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	<front>
		<journal-meta>
			<journal-id journal-id-type="publisher-id">rfmun</journal-id>
			<journal-title-group>
				<journal-title>Revista de la Facultad de Medicina</journal-title>
				<abbrev-journal-title abbrev-type="publisher">rev.fac.med.</abbrev-journal-title>
			</journal-title-group>
			<issn pub-type="ppub">0120-0011</issn>
			<publisher>
				<publisher-name>Universidad Nacional de Colombia</publisher-name>
			</publisher>
		</journal-meta>
		<article-meta>
			<article-id pub-id-type="other">400</article-id>
			<article-id pub-id-type="doi">10.15446/revfacmed.v70n1.97560</article-id>
			<article-categories>
				<subj-group subj-group-type="heading">
					<subject>Reflection article</subject>
				</subj-group>
			</article-categories>
			<title-group>
				<article-title>Delta variant of SARS-CoV-2: characteristics and implications for public health in Colombia</article-title>
				<trans-title-group xml:lang="es">
					<trans-title>Variante delta del SARS-CoV-2: características e implicaciones para la salud pública en Colombia</trans-title>
				</trans-title-group>
			</title-group>
			<contrib-group>
				<contrib contrib-type="author">
					<contrib-id contrib-id-type="orcid">0000-0003-2886-8146</contrib-id>
					<name>
						<surname>Yomayusa</surname>
						<given-names>Nancy</given-names>
					</name>
					<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
					<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
				</contrib>
				<contrib contrib-type="author">
					<contrib-id contrib-id-type="orcid">0000-0002-7632-6723</contrib-id>
					<name>
						<surname>Vega</surname>
						<given-names>Roman</given-names>
					</name>
					<xref ref-type="aff" rid="aff3"><sup>3</sup></xref>
					<xref ref-type="aff" rid="aff4"><sup>4</sup></xref>
				</contrib>
				<contrib contrib-type="author">
					<contrib-id contrib-id-type="orcid">0000-0002-3718-4558</contrib-id>
					<name>
						<surname>Restrepo-Henao</surname>
						<given-names>Alexandra</given-names>
					</name>
					<xref ref-type="aff" rid="aff5"><sup>5</sup></xref>
					<xref ref-type="corresp" rid="c1"><sup>*</sup></xref>
				</contrib>
				<contrib contrib-type="author">
					<contrib-id contrib-id-type="orcid">0000-0002-5044-7252</contrib-id>
					<name>
						<surname>Morón</surname>
						<given-names>Lina</given-names>
					</name>
					<xref ref-type="aff" rid="aff1"><sup>1</sup></xref>
					<xref ref-type="aff" rid="aff2"><sup>2</sup></xref>
				</contrib>
				<contrib contrib-type="author">
					<contrib-id contrib-id-type="orcid">0000-0001-5489-2671</contrib-id>
					<name>
						<surname>Vaca</surname>
						<given-names>Claudia</given-names>
					</name>
					<xref ref-type="aff" rid="aff6"><sup>6</sup></xref>
				</contrib>
				<contrib contrib-type="author">
					<contrib-id contrib-id-type="orcid">0000-0002-6180-792X</contrib-id>
					<name>
						<surname>Oñate</surname>
						<given-names>José</given-names>
					</name>
					<xref ref-type="aff" rid="aff7"><sup>7</sup></xref>
				</contrib>
			</contrib-group>
			<aff id="aff1">
				<label>1</label>
				<institution content-type="original"> Keralty Instituto Global de Excelencia Clínica - Translational Research Group - Bogotá D.C. - Colombia.</institution>
				<institution content-type="orgname">Keralty Instituto Global de Excelencia Clínica</institution>
				<addr-line>
					<city>Bogotá</city>
					<state>D.C</state>
				</addr-line>
				<country country="CO">Colombia</country>
			</aff>
			<aff id="aff2">
				<label>2</label>
				<institution content-type="original"> Grupo Keralty - Fundación Universitaria Sanitas - Bogotá D.C. - Colombia.</institution>
				<institution content-type="orgname">Fundación Universitaria Sanitas</institution>
				<addr-line>
					<city>Bogotá</city>
					<state>D.C</state>
				</addr-line>
				<country country="CO">Colombia</country>
			</aff>
			<aff id="aff3">
				<label>3</label>
				<institution content-type="original"> Pontificia Universidad Javeriana - Faculty of Social Sciences - Interdisciplinary Doctórate in Social and Human Sciences - Bogotá D.C. - Colombia.</institution>
				<institution content-type="normalized">Pontificia Universidad Javeriana</institution>
				<institution content-type="orgname">Pontificia Universidad Javeriana</institution>
				<institution content-type="orgdiv1">Faculty of Social Sciences</institution>
				<addr-line>
					<city>Bogotá</city>
					<state>D.C</state>
				</addr-line>
				<country country="CO">Colombia</country>
			</aff>
			<aff id="aff4">
				<label>4</label>
				<institution content-type="original"> Pontificia Universidad Javeriana - Public Health Institute - Bogotá D.C. - Colombia.</institution>
				<institution content-type="normalized">Pontificia Universidad Javeriana</institution>
				<institution content-type="orgname">Pontificia Universidad Javeriana</institution>
				<addr-line>
					<city>Bogotá</city>
					<state>D.C</state>
				</addr-line>
				<country country="CO">Colombia</country>
			</aff>
			<aff id="aff5">
				<label>5</label>
				<institution content-type="original"> Universidad de Antioquia - National School of Public Health - Epidemiology Research Group - Medellín - Colombia.</institution>
				<institution content-type="normalized">Universidad de Antioquia</institution>
				<institution content-type="orgname">Universidad de Antioquia</institution>
				<addr-line>
					<city>Medellín -</city>
				</addr-line>
				<country country="CO">Colombia</country>
			</aff>
			<aff id="aff6">
				<label>6</label>
				<institution content-type="original"> Universidad Nacional de Colombia - Bogotá Campus - Faculty of Sciences - Centro de Pensamiento Medicamentos, Información y Poder - Bogotá D.C. - Colombia.</institution>
				<institution content-type="normalized">Universidad Nacional de Colombia</institution>
				<institution content-type="orgname">Universidad Nacional de Colombia</institution>
				<institution content-type="orgdiv1">Faculty of Sciences</institution>
				<addr-line>
					<city>Bogotá</city>
					<state>D.C</state>
				</addr-line>
				<country country="CO">Colombia</country>
			</aff>
			<aff id="aff7">
				<label>7</label>
				<institution content-type="original"> Asociación Colombiana de Infectología - Presidency - Bogotá D.C. - Colombia.</institution>
				<institution content-type="orgname">Asociación Colombiana de Infectología</institution>
				<addr-line>
					<city>Bogotá</city>
					<state>D.C</state>
				</addr-line>
				<country country="CO">Colombia</country>
			</aff>
			<author-notes>
				<corresp id="c1">
					<label>*</label><bold>Corresponding author:</bold> Alexandra Restrepo-Henao. Grupo de Investigación en Epidemiología, Facultad Nacional de Salud Pública, Universidad de Antioquia. Medellín. Colombia. Email: <email>cheres80@gmail.com</email>.</corresp>
				<fn fn-type="conflict" id="fn3">
					<label>Conflicts of interest</label>
					<p> None stated by the authors. </p>
				</fn>
			</author-notes>
			<pub-date date-type="pub" publication-format="electronic">
				<day>06</day>
				<month>09</month>
				<year>2022</year>
			</pub-date>
			<pub-date date-type="collection" publication-format="electronic">
				<season>Jan-Mar</season>
				<year>2022</year>
			</pub-date>
			<volume>70</volume>
			<issue>1</issue>
			<elocation-id>e400</elocation-id>
			<history>
				<date date-type="received">
					<day>25</day>
					<month>07</month>
					<year>2021</year>
				</date>
				<date date-type="accepted">
					<day>10</day>
					<month>09</month>
					<year>2021</year>
				</date>
			</history>
			<permissions>
				<license license-type="open-access" xlink:href="https://creativecommons.org/licenses/by/4.0/" xml:lang="en">
					<license-p>This is an open-access article distributed under the terms of the Creative Commons Attribution License</license-p>
				</license>
			</permissions>
			<abstract>
				<title><italic>Abstract</italic></title>
				<p>The SARS-CoV-2 Delta variant has become one of the greatest public health challenges worldwide since, after being first identified in India in December 2020, it has spread rapidly, affecting mainly countries with low vaccination rates and those that have relaxed the public health and social measures implemented to control the COVID-19 pandemic.</p>
				<p>The Delta variant has a higher replication capacity and is associated with viral loads up to 1 260 times higher than those of infections caused by the original strain, which may be associated with an increased likelihood of hospitalization, ICU admission, need for oxygen therapy, pneumonia, or even death.</p>
				<p>Fully vaccinated individuals have almost similar protection against both Delta and Alpha variants. Given the impact of Delta in countries where it is the dominant variant, it is necessary for all countries to develop systematic action plans focused on implementing strict public health and social measures in the context of the COVID-19 pandemic and on increasing vaccination coverage. Bearing this in mind, the objective of this reflection paper is to describe the main characteristics of the Delta variant, its impact on the dynamics of the pandemic in some of the countries where it has been detected, the effectiveness of vaccines against this variant, and its implications for public health in Colombia.</p>
			</abstract>
			<trans-abstract xml:lang="es">
				<title><italic>Resumen</italic></title>
				<p>La variante delta del SARS-CoV-2 se ha convertido en uno de los mayores desafíos en salud pública a nivel mundial, ya que, luego de su identificación en la India en diciembre de 2020, se ha extendido de manera rápida, afectando principalmente a los países con bajas tasas de vacunación, y aquellos que han flexibilizado las medidas de salud pública establecidas para controlar la pandemia por COVID-19.</p>
				<p>La variante delta tiene una mayor capacidad de replicación y se asocia con cargas virales hasta 1 260 veces más altas en comparación con las de infecciones causadas por la cepa original, lo cual puede estar asociado a mayores probabilidades de hospitalización, ingreso a UCI, necesidad de oxigenoterapia, neumonía, o incluso muerte.</p>
				<p>Las personas con vacunación completa tienen una protección casi similar contra las variantes delta y alfa. Dado el impacto de delta en los países afectados en los que es la variante dominante, es necesario que todos los países desarrollen planes de acción sistemáticos enfocados en implementar estrictas medidas de salud pública y sociales en el contexto de la pandemia por COVID-19, y aumentar la cobertura de vacunación. Teniendo en cuenta lo anterior, el objetivo de esta reflexión es describir las principales características de la variante delta, su impacto en la dinámica de la pandemia en algunos de los países en que ha sido detectada, la efectividad de las vacunas contra esta variante, y sus implicaciones para la salud pública en Colombia.</p>
			</trans-abstract>
			<kwd-group xml:lang="en">
				<title>Keywords:</title>
				<kwd>SARS-CoV-2</kwd>
				<kwd>COVID-19</kwd>
				<kwd>Pandemic</kwd>
				<kwd>Public Health (MeSH)</kwd>
			</kwd-group>
			<kwd-group xml:lang="es">
				<title>Palabras clave:</title>
				<kwd>SARS-CoV-2</kwd>
				<kwd>COVID-19</kwd>
				<kwd>Pandemia</kwd>
				<kwd>Salud pública (DeCS)</kwd>
			</kwd-group>
			<counts>
				<fig-count count="0"/>
				<table-count count="1"/>
				<equation-count count="0"/>
				<ref-count count="56"/>
				<page-count count="0"/>
			</counts>
		</article-meta>
	</front>
	<body>
		<sec sec-type="intro">
			<title>Introduction</title>
			<p>The Delta variant of SARS-CoV-2 has spread rapidly in some countries where social and public health measures to control the COVID-19 pandemic have become more flexible. This variant has led to an increase in the number of cases and mortality and, as a result, to the collapse of health systems, particularly in low- and middle-income countries.</p>
			<p>The countries most affected by the Delta variant have limited vaccination coverage and were already dealing with the severe impact of the third wave of the pandemic, which exacerbated the lack of resources and increased the fatigue of health professionals.<xref ref-type="bibr" rid="B1"><sup>1</sup></xref><sup>,</sup><xref ref-type="bibr" rid="B2"><sup>2</sup></xref>
			</p>
			<p>Phylogenic analysis performed on the complete genome of SARS-CoV-2, identified on January 3, 2020, by scientists at the National Institute for Viral Disease Control and Prevention in China, confirmed that it is a novel coronavirus of the genus β(2019-nCoVs).<xref ref-type="bibr" rid="B3"><sup>3</sup></xref>
			</p>
			<p>The World Health Organization (WHO) has worked with networks of experts around the world to assess the evolution of SARS-CoV-2. In doing so, variants that pose an increased risk to global public health have been identified and termed &quot;variants of interest&quot; (VOI) and &quot;variants of concern&quot; (VOC). A third category, called &quot;variants under monitoring&quot; (VUM) was also established, including variants that may pose a risk to global public health but for which there is still insufficient evidence of their epidemiological impact.<xref ref-type="bibr" rid="B4"><sup>4</sup></xref>
			</p>
			<p>WHO<xref ref-type="bibr" rid="B5"><sup>5</sup></xref> defines VOIs as those variants with changes in the genome that have been shown or are expected to have an impact on certain characteristics of the virus such as transmissibility, disease severity, the ability to escape the action of the immune system, the possibility of being detected by diagnostic methods, and changes in response to medications. In this sense, it is necessary to monitor variants that have an increasing relative prevalence with respect to others, or those with characteristics that indicate that they may pose a new risk to global public health.<xref ref-type="bibr" rid="B6"><sup>6</sup></xref>
			</p>
			<p>On the other hand, a VOC is defined as a variant associated with one or more of the following changes: 1) increased transmissibility or adverse change in the epidemiology of COVID-19, 2) increased virulence or change in the clinical presentation of the disease, and 3) decreased efficacy of public health measures implemented to counter its spread, or decreased effectiveness of diagnoses, vaccines or therapies.<xref ref-type="bibr" rid="B6"><sup>6</sup></xref>
			</p>
			<p>The Delta variant (B.1.617.2) was first reported in December 2020 in India, where it caused a public health crisis. It has quickly become the dominant variant in the places where it has been identified because it is more transmissible: it is 40-60% more contagious than the Alpha variant (B.1.1.7).<xref ref-type="bibr" rid="B7"><sup>7</sup></xref><sup>,</sup><xref ref-type="bibr" rid="B8"><sup>8</sup></xref>
			</p>
			<p>Similarly, Delta has the potential to be more lethal because it is associated with more cases, greater capacity to bind to lung cell receptors, and a possible reduction in response to antibody neutralization, including some of the monoclonal antibodies available for treatment.<xref ref-type="bibr" rid="B9"><sup>9</sup></xref><sup>,</sup><xref ref-type="bibr" rid="B10"><sup>10</sup></xref> Furthermore, it affects vulnerable populations more, particularly in countries with fragile health systems, without strong and predictive public health policies, and with low rates of vaccination against COVID-19. For all of the reasons listed above, WHO declared Delta a VOC on May 24, 2021.<xref ref-type="bibr" rid="B4"><sup>4</sup></xref><sup>,</sup><xref ref-type="bibr" rid="B11"><sup>11</sup></xref>
			</p>
			<p>Delta has rapidly become the dominant lineage in the countries in which it has emerged. According to WHO,<xref ref-type="bibr" rid="B11"><sup>11</sup></xref> as of June 27, 2021, Delta had been reported in 96 countries, although this is likely to be an underestimate as the sequencing capabilities required to identify variants are limited. In the same report, WHO also indicated that several of the countries with Delta are attributing surges in infections and hospitalizations to this variant,<xref ref-type="bibr" rid="B11"><sup>11</sup></xref> and, in fact, as of July 25, 2021, Delta had already been detected in 130 countries, including Colombia.<xref ref-type="bibr" rid="B12"><sup>12</sup></xref>
			</p>
			<p>Considering the above, the objective of this reflection is to describe the main characteristics of the SARS-CoV-2 Delta variant, how the dynamics of the pandemic has changed in some of the countries where it has been detected, as well as the effectiveness of vaccines against this variant and its implications for public health in Colombia.</p>
			<sec>
				<title>Is the Delta variant more contagious?</title>
				<p>The Delta variant spreads 40-60% faster than Alpha.<xref ref-type="bibr" rid="B7"><sup>7</sup></xref><sup>,</sup><xref ref-type="bibr" rid="B8"><sup>8</sup></xref> This increased transmissibility can be explained by changes in its constituent proteins, since Delta has mutations in the receptor-binding domain (RBD) of protein S (L452R, E484Q, and D614G being the main ones), which interacts with the angiotensin-converting enzyme receptor 2 (ACE2) in host cells. This results in a noticeable increase in transmissibility due to greater affinity and significant conformational changes important for binding with ACE2.<xref ref-type="bibr" rid="B13"><sup>13</sup></xref> The P681R mutation, located at the furin cleavage site, has also been identified; this mutation optimizes the cleavage of protein S by furin, which ultimately results in increased transmissibility and pathogenicity.<xref ref-type="bibr" rid="B14"><sup>14</sup></xref> Transmission of infection in people with Delta takes seconds and occurs at a shorter distance compared to the Alpha variant, which required at least 15 minutes of contact and a distance of &lt;1.5m.<xref ref-type="bibr" rid="B15"><sup>15</sup></xref>
				</p>
				<p>The latest report from the Imperial College of London and studies from the University of Warwick and the London School of Hygiene and Tropical Medicine (LSHTM)<xref ref-type="bibr" rid="B16"><sup>16</sup></xref><sup>-</sup><xref ref-type="bibr" rid="B19"><sup>19</sup></xref> suggest that by June 2021 it had become the dominant variant in the UK. According to mathematical modeling carried out by these institutions, in England, it is estimated that the effective reproduction number (R) for the Alpha variant is approximately 0.8, while for Delta it is 1.5, with an overall R value of around 1.4 for both variants. In view of the above, they recommend strengthening public health measures to reduce the number of cases and deaths, as well as ensuring that all countries work together to control global transmission by promoting equitable access to vaccines, thus preventing the emergence of new variants that would perpetuate the severity of subsequent waves of infection.</p>
			</sec>
			<sec>
				<title>Is the Delta variant a threat to populations with inadequate vaccination coverage?</title>
				<p>In April 2021, the United Kingdom was preparing to open spaces for the development of economic and social activities as the numbers of cases, hospitalizations and deaths due to COVID-19 had decreased; however, after the first cases of the Delta variant were detected, economic and social reactivation plans were suspended. By June 14, 2021, Delta already accounted for 91% of cases in that country, and it had been established that children and adults under 50 years of age were 2.5 times more likely to be infected with this variant.<xref ref-type="bibr" rid="B9"><sup>9</sup></xref><sup>,</sup><xref ref-type="bibr" rid="B20"><sup>20</sup></xref><sup>,</sup><xref ref-type="bibr" rid="B21"><sup>21</sup></xref>
				</p>
				<p>Despite the millions of doses of COVID-19 vaccines administered in the United States, the Delta variant is a real threat there given the large disparities and inequities in health care and access to vaccination, the vulnerability of ethnic minorities, the influence of anti-vaccine movements, and the low vaccination coverage in adolescents (&lt;10%).<xref ref-type="bibr" rid="B22"><sup>22</sup></xref>
				</p>
				<p>Cases of COVID-19 in the United States have increased mainly in territories with low vaccination rates. In this regard, the Centers for Disease Control and Prevention (CDC)<xref ref-type="bibr" rid="B23"><sup>23</sup></xref> reported that the weekly number (7 days) of hospitalizations for COVID-19 has been steadily increasing since June 25, 2021, and that between July 21 and July 27, 2021, there were 5 475 hospitalizations, which represented an increase of 46.3% compared to the figure reported in the previous week (from July 14 to 20; n=3 742). In addition, when comparing the week of July 21 to 27 with that of July 14 to 21, there was also a 64.1% increase in the number of new cases (66 606 vs. 40 597) and a 33.3% increase in the number of deaths from this disease (296 vs. 222). Finally, according to the CDC, and based on preliminary data, weekly hospitalization rates for COVD-19 have increased significantly in adults aged 18 to 49 years, rising by nearly 40% between the week ending June 26 and the week ending July 10, 2021.</p>
				<p>Bolze <italic>et al.</italic><xref ref-type="bibr" rid="B24"><sup>
 <italic>24</italic>
</sup></xref> established, by sequencing 19 987 samples obtained in the United States since April 2021, that Delta spread faster in counties with a low vaccination rate (defined as less than 28.5% of residents with a full vaccination schedule as of May 1), compared with those with a high vaccination rate (&gt;28.5%).</p>
			</sec>
			<sec>
				<title>Do people infected with the Delta variant have different manifestations and a greater likelihood of hospitalization and death?</title>
				<p>THE ZOE Health Study<xref ref-type="bibr" rid="B25"><sup>25</sup></xref> reported that there are some differences between classic and specific symptoms of the Delta variant, since headache, sore throat, runny nose and fever are more frequent with the latter, while cough and loss of smell are less common.</p>
				<p>In a study conducted in Scotland, Sheikh <italic>et al.</italic><xref ref-type="bibr" rid="B26"><sup>
 <italic>26</italic>
</sup></xref> established that, compared with people infected with Alpha, Delta cases had an increased risk of hospital admission due to COVID-19 (HR: 1.85; 95%CI: 1.39-2.47) after adjusting the Cox regression model for age, sex, deprivation, temporal trend, and comorbidities. These authors also found that the risk of hospital admission was particularly higher in patients with 5 or more relevant comorbidities.</p>
				<p>Similarly, based on a record linkage of sequence-confirmed Delta and Alpha cases in England analyzed between March 29 and May 23, 2021, and with hospitalization data up until June 5, 2021, a preliminary analysis of 43 338 cases found that there was a significantly increased risk of hospitalization within 14 days after taking the sample (HR: 2.26; 95%CI: 1.32-3.89) for Delta compared to Alpha cases after adjustment for confounding variables (age, sex, ethnicity, area of residence, vaccination status).<xref ref-type="bibr" rid="B27"><sup>27</sup></xref>
				</p>
				<p>Moreover, in an analysis of surveillance data on all COVID-19 cases reported to the European Surveillance System by 10 countries for the period between December 28, 2020, and May 16, 2021, the hospitalization rate was 3.3% for cases aged 40 to 49 years and then nearly doubled with the increase of the decade of age, reaching 25.3% for people aged 70 to 79 years and 36.2% for those aged 80 and over. In addition, during the same study period, cases aged 50 years or older accounted for 39% of all cases and 83% of hospital admissions.<xref ref-type="bibr" rid="B28"><sup>28</sup></xref>
				</p>
				<p>Likewise, in Ontario, Canada, Fisman &amp; Tuite<xref ref-type="bibr" rid="B29"><sup>29</sup></xref> estimated the risk of hospitalization caused by the Delta variant using a retrospective cohort of patients who tested positive for SARSCoV-2 and screened for VOC between February 7 and June 22, 2021 (n=211 197). They found that, compared with non-VOC SARS-CoV-2 strains, the adjusted increase of the risk associated with N501Y-positive variants was 59% (95%CI: 49-69) for hospital admission, 105% (95%CI: 82-134) for admission to the intensive care unit (ICU), and 61% (95%CI: 40-87) for death.</p>
				<p>Finally, in the United Kingdom, according to a technical report from Public Health England, a case fatality rate of 0.2% (95%CI: 0.2-0.3) was reported on July 5, 2021, after 28 days of follow-up among cases with the Delta variant, whereas the case fatality rate in cases infected with the Alpha variant was 1.9% (95%CI: 1.8-2.0).<xref ref-type="bibr" rid="B15"><sup>15</sup></xref> However, these are preliminary studies and further evidence is required to conclude whether fatality is similar or not for these two variants.</p>
			</sec>
			<sec>
				<title>Are vaccines effective against the Delta variant?</title>
				<p>The emergence of new VOC of SARS-CoV-2 poses a potential threat to the effectiveness of available vaccines. Evidence shows that people who have only received the first dose of a two-dose scheme are less protected against Delta-variant infection, regardless of the type of vaccine. However, full vaccination provides very similar protection against the Delta and Alpha variants. <xref ref-type="bibr" rid="B26"><sup>26</sup></xref><sup>,</sup><xref ref-type="bibr" rid="B30"><sup>30</sup></xref><sup>,</sup><xref ref-type="bibr" rid="B31"><sup>31</sup></xref>
				</p>
				<p>In this regard, Lopez-Bernal <italic>et</italic> al.,<xref ref-type="bibr" rid="B30"><sup>30</sup></xref> in a case-control study of negative tests carried out to estimate the effectiveness of vaccination against symptomatic disease caused by the Delta and Alpha variants, established that the effectiveness of one dose of Pfizer-BioNTech and Oxford/AstraZeneca BNT162b2 vaccines was significantly lower among people with Delta (30.7%; 95%CI: 25.2-35.7) than among people with Alpha (48.7%; 95%CI: 45.5-51.7). The authors also found that the results for two doses of both vaccines were similar: the effectiveness of the Pfizer-BioNTech vaccine was 93.7% (95%CI: 91.6-95.3) among people with Alpha and 88.0% (95%CI: 85.3-90.1) among those with Delta, whereas the effectiveness of two doses of Oxford/AstraZeneca was 74.5% (95%CI: 68.4-79.4) among people with Alpha and 67.0% (95%CI: 61.3-71.8) among people with Delta.<xref ref-type="bibr" rid="B30"><sup>30</sup></xref>
				</p>
				<p>In turn, Stowe <italic>et</italic> al.,<xref ref-type="bibr" rid="B32"><sup>32</sup></xref> in a study that included 14 019 symptomatic cases of the Delta variant between April 12 and June 4, 2021, in England, reported that the effectiveness of the Pfizer-BioNTech vaccine against hospitalization was 94% after one dose and 96% after two doses, while the effectiveness of the Oxford/AstraZeneca vaccine was 71% after one dose and 92% after two doses.</p>
				<p>Finally, in a cohort study conducted to describe the demographic profile of patients with COVID-19, investigate the risk of hospital admission due to COVID-19, and estimate the effectiveness of the vaccine in preventing hospital admissions due to COVID-19 in cases with the Delta variant, Sheikh <italic>et al.</italic><xref ref-type="bibr" rid="B26"><sup>
 <italic>26</italic>
</sup></xref> found that, compared with unvaccinated individuals, at least 14 days after the second dose, the Pfizer-BioNTech vaccine offered 79% protection against the Delta variant and 92% protection against the Alpha variant, while the protection offered by the Oxford/AstraZeneca vaccine was 60% against Delta and 73% against Alpha.</p>
				<p>This shows that, as with all known variants, complete vaccination schedules work against the Delta variant and prevent severe presentations of the disease. Therefore, given the high transmissibility of Delta, in countries with greater social inequities and low vaccination coverage, the risk of contagion is maintained and the risk of hospitalization increases (<xref ref-type="table" rid="t1">Table 1</xref>).</p>
				<p>
					<table-wrap id="t1">
						<label>Table 1</label>
						<caption>
							<title>Characteristics of the Delta variant in relation to the vaccines.</title>
						</caption>
						<table>
							<colgroup>
								<col/>
								<col/>
							</colgroup>
							<thead>
								<tr>
									<th align="center">Characteristics</th>
									<th align="center">Delta variant</th>
								</tr>
							</thead>
							<tbody>
								<tr>
									<td align="left">Transmissibility</td>
									<td align="left">Increased transmissibility and secondary attack <xref ref-type="bibr" rid="B15">rate<sup>15</sup></xref><sup>,</sup><xref ref-type="bibr" rid="B20"><sup>20</sup></xref>
									</td>
								</tr>
								<tr>
									<td align="left">Severity of the disease</td>
									<td align="left">Possible increased risk of hospitalization</td>
								</tr>
								<tr>
									<td align="left">Risk of reinfection</td>
									<td align="left">Reduction of the neutralizing activity of vaccines<xref ref-type="bibr" rid="B10"><sup>10</sup></xref>
									</td>
								</tr>
								<tr>
									<td align="left">Impact on diagnostic methods</td>
									<td align="left">None reported</td>
								</tr>
								<tr>
									<td align="left">Efficacy/Effectiveness (%)</td>
									<td align="left">Protection against severe COVID-19 remains the same, but protection against symptomatic disease and infection may be reduced</td>
								</tr>
								<tr>
									<td align="left">Severe disease</td>
									<td align="left">Oxford/AstraZeneca and Pfizer-BioNTech: reduction in efficacy &lt;10% or efficacy &gt;90% without comparator, or &lt;2-fold reduction in neutralization<xref ref-type="bibr" rid="B32"><sup>32</sup></xref>
									</td>
								</tr>
								<tr>
									<td align="left">Symptomatic disease</td>
									<td align="left">
										<p>
											<list list-type="simple">
												<list-item>
													<p>Pfizer-BioNTech: reduction in efficacy &lt;10% or efficacy &gt;90% without comparator, or &lt;2-fold reduction in neutralization<xref ref-type="bibr" rid="B26"><sup>26</sup></xref>. Reduction in efficacy from 10% to &lt;20%, or 2-fold to &lt;5-fold reduction in neutralization<xref ref-type="bibr" rid="B30"><sup>30</sup></xref>
													</p>
												</list-item>
												<list-item>
													<p>Oxford/AstraZeneca: reduction in efficacy from 20% to &lt;30%, or 5-fold to &lt;10-fold reduction in neutralization<xref ref-type="bibr" rid="B29"><sup>29</sup></xref><sup>,</sup><xref ref-type="bibr" rid="B31"><sup>31</sup></xref>
													</p>
												</list-item>
											</list>
										</p>
									</td>
								</tr>
								<tr>
									<td align="left">Infections</td>
									<td align="left">Oxford/AstraZeneca and Pfizer-BioNTech: reduction in efficacy from 10% to &lt;20%, or 2 to &lt;5-fold reduction in neutralization<xref ref-type="bibr" rid="B31"><sup>31</sup></xref>
									</td>
								</tr>
								<tr>
									<td align="left">Neutralization</td>
									<td align="left">
										<p>
											<list list-type="simple">
												<list-item>
													<p>Janssen-Ad.COV 2.5: &lt;2-fold reduction in neutralization<xref ref-type="bibr" rid="B33"><sup>33</sup></xref>
													</p>
												</list-item>
												<list-item>
													<p>AstraZeneca-Vaxzevria and Moderna-mRNA-1273: 2 to &lt;5-fold reduction in neutralization <xref ref-type="bibr" rid="B34"><sup>34</sup></xref><sup>-</sup><xref ref-type="bibr" rid="B36"><sup>36</sup></xref> Pfizer-BioNTech: 2 to &lt;5-fold reduction in neutralization, or 5 to &lt;10-fold or more reduction in neutralization</p>
												</list-item>
											</list>
										</p>
									</td>
								</tr>
							</tbody>
						</table>
						<table-wrap-foot>
							<fn id="TFN1">
								<p>Source: Own elaboration.</p>
							</fn>
						</table-wrap-foot>
					</table-wrap>
				</p>
			</sec>
			<sec>
				<title>What are the characteristics of the immune response to vaccines in vaccinated people?</title>
				<p>Adaptive humoral and cell-mediated immune responses to infections depend on the pathogen and protect against future reinfections. Thus, vaccine-induced immune responses are usually multifaceted; however, most of the currently accepted correlates of protection are based on antibody measurements.<xref ref-type="bibr" rid="B37"><sup>37</sup></xref> Although it is known that these correlates are not the only mechanism of protection, they are often much easier to measure than cellular responses and, therefore, neutralizing antibody responses to SARS-CoV-2 are analyzed in most studies to evaluate the efficacy of vaccines against this virus.<xref ref-type="bibr" rid="B34"><sup>34</sup></xref>
				</p>
				<p>Results from a neutralizing antibody titer assay suggested that titers in people who received two doses of the vaccine decreased by 5.8-fold against the Delta variant compared to wild-type virus when the Pfizer-BioNTech vaccine was used.<xref ref-type="bibr" rid="B38"><sup>38</sup></xref>
				</p>
				<p>Jongeneelen <italic>et al.</italic><xref ref-type="bibr" rid="B33"><sup>33</sup></xref> analyzed sera from recipients of a single dose of Ad26.COV2.S/Janssen vaccine to determine the neutralizing activity against several SARS-CoV-2 VOCs and found that Delta showed only a 1.6-fold reduction in neutralization sensitivity. However, Tada <italic>et al.</italic><xref ref-type="bibr" rid="B39"><sup>
 <italic>39</italic>
</sup></xref> reported that neutralizing antibody titers were decreased by 5.4-fold for Delta.</p>
				<p>On the other hand, Barouch <italic>et al.,</italic><xref ref-type="bibr" rid="B31"><sup>
 <italic>31</italic>
</sup></xref> based on a study of 25 participants -20 who received 1 or 2 doses of the Ad26.COV2.S/Janssen vaccine (either 5x1010 viral particles or 1011 viral particles) and 5 who received placebo- reported that this vaccine caused long-lasting humoral and cellular immune responses with minimal decreases for at least 8 months after immunization, and that there was also an expansion of the amplitude of neutralizing antibodies against the Delta, Beta, and Gamma variants. This suggests maturation of B cell responses, even without additional booster.</p>
				<p>In a study intended to update on the neutralization activity of the mRNA-1273/Moderna vaccine sera against some newly emerged variants (including Delta) compared to the neutralization of wild-type SARS-CoV-2 virus, Choi <italic>et al.</italic><xref ref-type="bibr" rid="B40"><sup>
 <italic>40</italic>
</sup></xref> found minimal effects on neutralization titers against Alpha (1.2-fold reduction compared to wild-type variant); but they observed reductions in neutralization of titers ranging from 2.1 to 8.4 times for the Beta, Delta and Gamma variants, compared to the wild-type variant, although all remained susceptible to serum neutralization caused by this vaccine.</p>
			</sec>
			<sec>
				<title>What is the viral load in people with the Delta variant and how is it affected by vaccination?</title>
				<p>So far, evidence shows that the Delta variant has greater transmissibility, which may be associated with a mutation found in its spike<xref ref-type="bibr" rid="B41"><sup>41</sup></xref> and a higher viral load.</p>
				<p>Li <italic>et al.</italic><xref ref-type="bibr" rid="B42"><sup>
 <italic>42</italic>
</sup></xref> conducted a study that characterized a large transmission chain that originated from the first local infection of the SARS-CoV-2 Delta variant in mainland China and found evidence of a potentially higher viral replication rate of this variant because viral loads in Delta infections are about 1 000 times higher than those of infections with other variants on the day of the first positive PCR test.</p>
				<p>Brown <italic>et al.</italic><xref ref-type="bibr" rid="B43"><sup>
 <italic>43</italic>
</sup></xref> published an analysis of an outbreak of SARS-CoV-2 infections in Barnstable County, Massachusetts, in July 2021. According to this report, vaccination coverage among Massachusetts residents was 69%, and 469 COVID-19 cases were associated with various cultural events with a large number of attendees in a town in this county. Of these 469 cases, 74% occurred in people who were fully vaccinated (46% with Pfizer, 38% with Moderna, and 16% with Janssen). In addition, 113 patients underwent initial genomic sequencing of specimens, which identified the Delta variant in 119 (89%) cases and the Delta AY.3 sublineage in one case (1%); genomic sequencing was unsuccessful in 13 (10%) specimens. In general, the symptoms of the people infected were mild and only 5 patients were hospitalized, 4 of whom were fully vaccinated.</p>
			</sec>
			<sec>
				<title>What is the risk of the Delta variant in countries that relax social and public health measures implemented to control the spread of SARS-CoV-2?</title>
				<p>The Delta variant is spreading rapidly as some countries reactivate their economic and social activities and make public health measures more flexible, as these actions undoubtedly lead to an increased risk of viral transmission and, thus, to an increase in the number of cases, hospitalizations, and deaths.<xref ref-type="bibr" rid="B44"><sup>44</sup></xref>
				</p>
				<p>Model based analyzes conducted in the United Kingdom<xref ref-type="bibr" rid="B45"><sup>45</sup></xref><sup>-</sup><xref ref-type="bibr" rid="B49"><sup>49</sup></xref> indicate that any relaxation of non-pharmacological measures implemented to control the spread of SARS-CoV-2 could lead to a rapid and significant increase in daily cases in all age groups, with a higher incidence in people under 50 years of age, particularly young people, and an associated increase in the number of hospitalizations. Therefore, it is of vital importance to avoid the relaxation of these measures, which include isolation, quarantine, testing, follow-up of positive cases, the use of face masks, social distancing, and the promotion of respiratory hygiene measures.</p>
				<p>In this sense, despite the risk that the Delta variant implies for world public health, the reduction in the rigor of social and public health measures in many countries without complete vaccination coverage in people at greater risk is striking.<xref ref-type="bibr" rid="B28"><sup>28</sup></xref>
				</p>
				<p>Baker <italic>et</italic> al.<xref ref-type="bibr" rid="B50"><sup>50</sup></xref> established that countries that implemented non-pharmacological interventions to eliminate SARS-CoV-2 transmission had better results in controlling the pandemic than those that opted for mitigation strategies, which aimed at establishing gradual measures to reduce cases and not overburdening health systems.</p>
				<p>Likewise, Oliu-Barton <italic>et al.,</italic><xref ref-type="bibr" rid="B51"><sup>
 <italic>51</italic>
</sup></xref> in a study comparing the number of deaths by COVID-19, gross domestic product (GDP) growth, and the strictness of containment measures during the first 12 months of the pandemic in Organisation for Economic Co-operation and Development (OECD) countries, found that COVID-19 deaths per million population in the 5 OECD countries that opted for the elimination of SARS-CoV-2 (Australia, Iceland, Japan, New Zealand, and South Korea) were about 25 times lower than in countries that favored SARS-CoV-2 mitigation.</p>
				<p>Oliu-Barton <italic>et al.</italic><xref ref-type="bibr" rid="B51"><sup>
 <italic>51</italic>
</sup></xref> also established that there is increasing consensus that elimination is preferable to mitigation in relation to a country's economic performance since they found that GDP growth returned to pre-pandemic levels in early 2021 in the 5 countries that opted for elimination, while growth remained negative for the other 32 countries.</p>
				<p>In this sense, it can be concluded that the countries that took preventive measures and acted quickly against local outbreaks were able to control the virus and reduce the impact on public health. However, given the complexity of the potential impact of Delta circulation, it is necessary to implement a multidimensional approach combining public health and social measures from different perspectives and disciplines.</p>
			</sec>
			<sec>
				<title>What can be learned in Colombia?</title>
				<p>On July 24, 2021, the first case of Delta in Colombia was reported, raising the need to assimilate the lessons learned in other countries in a timely manner to avoid the complications they have experienced with this variant. These lessons are mainly related to the fact that public health strategies that have been relaxed in recent months must be re-implemented, including isolation, testing, and promotion of vaccination.</p>
				<p>The Delta variant is yet further evidence of how SARS-CoV-2 continues to evolve to spread more rapidly. In this regard, it is important to bear in mind that this variant can be transmitted both in vaccinated and unvaccinated populations and, therefore, mass vaccination against COVID-19, although one of the most important measures to counteract its rapid spread, cannot be the only one. Considering this is also of paramount importance given that the impact of Delta may be much greater in Colombia, where COVID-19 vaccination coverage at the end of July 2021 is low compared to vaccination rates in England, where Delta quickly became dominant and its impact has caused major consequences; at this point, it should also be noted that public health measures have been relaxed there (reduction in capacity has been lifted and crowded events are performed).</p>
				<p>According to Lazarus,<xref ref-type="bibr" rid="B52"><sup>52</sup></xref> some members of the Lancet COVID-19 Commission working group on public health called for urgent action in response to the new variants: &quot;these new variants mean we cannot rely only on vaccines alone to provide protection but must maintain strong public health measures to reduce the risk from these variants. At the same time, we must accelerate the vaccine program in all countries in an equitable way.&quot; In this sense, the presence of VOIs requires a unified and non-isolated response from the competent entities, which should include the acceleration of vaccination and the implementation of effective non-pharmacological measures.</p>
				<p>Undoubtedly, evidence on the mechanisms involved in the transmission and morbidity and mortality of SARS-CoV-2 has increased considerably. However, the way this knowledge has been translated into the design of public health and containment policies is the subject of intense debate<xref ref-type="bibr" rid="B53"><sup>53</sup></xref> because there are multiple pressing, and often conflicting, societal objectives that create a fundamental problem when deciding on what aspects should be prioritized, such as short-term reduction of COVID-19 morbidity and mortality, mitigation of long-term social impacts caused by containment policies (increased social inequalities, mental health problems due to social isolation, lack of access to health services, and inter-generational conflicts), or adverse financial and social consequences.<xref ref-type="bibr" rid="B54"><sup>54</sup></xref><sup>,</sup><xref ref-type="bibr" rid="B55"><sup>55</sup></xref> For this reason, the COVID-19 pandemic has been considered a true &quot;wicked problem,&quot;<xref ref-type="bibr" rid="B56"><sup>56</sup></xref> since it not only caused an unprecedented global health crisis, but has also led to an economic and social crisis<xref ref-type="bibr" rid="B35"><sup>35</sup></xref> that is difficult to address from classical linear or traditional analytical approaches.</p>
				<p>Individual and community non-pharmacological interventions, such as mobility restrictions, testing strategies, tracing and isolation of confirmed cases and their contacts, as well as other social and biosecurity measures, have shown to be effective even in the absence of pharmacological interventions such as vaccines, because in countries where these first interventions have been consistently implemented, the results are positive and satisfactory, not only in reducing the incidence of infection and mortality rates, but in economic and social recovery.<xref ref-type="bibr" rid="B45"><sup>45</sup></xref><sup>,</sup><xref ref-type="bibr" rid="B46"><sup>46</sup></xref>
				</p>
				<p>On the basis of the evidence presented here, it could be said that the evolution of SARS-CoV-2 towards more transmissible, virulent and lethal variants, with a greater capacity to evade the host immune response, requires the development of multidimensional strategies that consider not only the control of the pandemic, but also the economic and social needs of the population. The design of these strategies should combine mass and rapid vaccination with non-pharmacological interventions and social support, education and assertive communication strategies that enable the empowerment and self-management of individuals, families and communities.</p>
				<p>Given the characteristics of Delta and because it has begun to be the dominant variant around the world, health systems in several countries, including those with high and moderate rates of vaccination coverage such as Israel, England, China, Australia, and New Zealand, have had to accelerate mass vaccination among uncovered populations (e.g. youth and adolescents) and implement public health and social strategies and non-pharmacological measures to control the spread of the pandemic and sustain the economic and social reactivation achieved.<xref ref-type="bibr" rid="B45"><sup>45</sup></xref><sup>,</sup><xref ref-type="bibr" rid="B47"><sup>47</sup></xref>
				</p>
				<p>In this sense, it is necessary to design synergistic and transdisciplinary solutions based on evidence and susceptible to systematic evaluation<xref ref-type="bibr" rid="B53"><sup>53</sup></xref> to solve the wicked problems created by the pandemic in Colombia. To achieve this, it is necessary to take into account that public health strategies during a pandemic, and any disaster, must be based on an analysis of the available evidence and take into account the economic and social consequences it may cause; therefore, their effectiveness should be evaluated before they are implemented.</p>
				<p>The following are some of the strategies that should be improved in order to respond adequately to the pandemic in the presence of the Delta variant in Colombia:</p>
				<p>
					<list list-type="order">
						<list-item>
							<p>The vaccination plan should be accelerated by ensuring compliance with complete schemes, particularly for vulnerable populations.</p>
						</list-item>
						<list-item>
							<p>Barriers to access to the vaccine in the global market must be overcome, requiring decisions to release patents and strengthen national production capacities.</p>
						</list-item>
						<list-item>
							<p>Effective and sustainable health surveillance measures should be put in place to control the potential circulation of the Delta variant, eliminate community-based transmission of SARS-CoV-2, and strengthen non-pharmacological interventions and primary health care aimed at preventing infection, detecting the virus early and managing cases and their contacts through tracing and isolation.</p>
						</list-item>
						<list-item>
							<p>Diagnostic testing capacity should be increased to detect positive cases so that they and their contacts can be adequately traced.</p>
						</list-item>
						<list-item>
							<p>Genomic surveillance of circulating variants should be strengthened, including weekly representative samples of sufficient size and specific samples from special environments and populations (travel-related cases or cases associated with a special clinical presentation and outbreaks).</p>
						</list-item>
						<list-item>
							<p>Control measures should be adopted for the entry of travelers; taking into account the evidence, the National Government should assess the country's vulnerability in terms of vaccination coverage and the circulation of new variants in order to determine whether or not measures should be implemented for travelers from other nations. These measures may include requesting RT-PCR tests and quarantine for five to seven days.</p>
						</list-item>
						<list-item>
							<p>Education and literacy programs aimed at the general community should be strengthened to enable people to understand the health implications of the new variant and to strengthen individual biosafety measures.</p>
						</list-item>
						<list-item>
							<p>The capacity of venues and enclosed areas should be monitored, and biosecurity controls that have been methodically planned and reviewed should be applied at workplaces, educational institutions, and recreation and cultural events.</p>
						</list-item>
						<list-item>
							<p>Finally, a panel discussion should be created with academics and experts from different disciplines to analyze the available evidence, support decision-making, and evaluate the public health measures implemented.</p>
						</list-item>
					</list>
				</p>
			</sec>
		</sec>
		<sec sec-type="conclusions">
			<title>Conclusions</title>
			<p>Due to its high transmissibility, Delta has become the dominant variant in the countries where it has been identified. This variant is associated with higher rates of transmission and mortality, and mainly affects unvaccinated people. However, available vaccines are effective in preventing severe forms of disease and death.</p>
			<p>In this regard, addressing the crisis and the impact of the pandemic, as well as the uncertainties raised by the evolution of SARS-CoV-2 and the emergence of new variants, requires a truly multidisciplinary and transdisciplinary approach that provides simultaneous solutions, which should be subject to frequent data-driven evaluation. Evidence-based public health containment measures to deal with the pandemic can be ethically justifiable and understood through a clear and transparent comprehension of the values underpinning political decisions.</p>
		</sec>
	</body>
	<back>
		<ack>
			<title>Acknowledgments</title>
			<p>None stated by the authors.</p>
		</ack>
		<ref-list>
			<title>References</title>
			<ref id="B1">
				<label>1</label>
				<mixed-citation>1. Boehm E, Kronig I, Neher RA, Eckerle I, Vetter P, Kaiser L. Novel SARS-CoV-2 variants: the pandemics within the pandemic. Clin Microbiol Infect. 2021;27(8):1109-17. <ext-link ext-link-type="uri" xlink:href="https://doi.org/gk7348">https://doi.org/gk7348</ext-link>.</mixed-citation>
				<element-citation publication-type="journal">
					<person-group person-group-type="author">
						<name>
							<surname>Boehm</surname>
							<given-names>E</given-names>
						</name>
						<name>
							<surname>Kronig</surname>
							<given-names>I</given-names>
						</name>
						<name>
							<surname>Neher</surname>
							<given-names>RA</given-names>
						</name>
						<name>
							<surname>Eckerle</surname>
							<given-names>I</given-names>
						</name>
						<name>
							<surname>Vetter</surname>
							<given-names>P</given-names>
						</name>
						<name>
							<surname>Kaiser</surname>
							<given-names>L</given-names>
						</name>
					</person-group>
					<article-title>Novel SARS-CoV-2 variants: the pandemics within the pandemic</article-title>
					<source>Clin Microbiol Infect</source>
					<year>2021</year>
					<volume>27</volume>
					<issue>8</issue>
					<fpage>1109</fpage>
					<lpage>1117</lpage>
					<ext-link ext-link-type="uri" xlink:href="https://doi.org/gk7348">https://doi.org/gk7348</ext-link>
				</element-citation>
			</ref>
			<ref id="B2">
				<label>2</label>
				<mixed-citation>2. Callaway E. Delta coronavirus variant: scientists brace for impact. Nature. 2021;595(7865):17-8. <ext-link ext-link-type="uri" xlink:href="https://doi.org/gkzc4t">https://doi.org/gkzc4t</ext-link>.</mixed-citation>
				<element-citation publication-type="journal">
					<person-group person-group-type="author">
						<name>
							<surname>Callaway</surname>
							<given-names>E</given-names>
						</name>
					</person-group>
					<article-title>Delta coronavirus variant: scientists brace for impact</article-title>
					<source>Nature</source>
					<year>2021</year>
					<volume>595</volume>
					<issue>7865</issue>
					<fpage>17</fpage>
					<lpage>18</lpage>
					<ext-link ext-link-type="uri" xlink:href="https://doi.org/gkzc4t">https://doi.org/gkzc4t</ext-link>
				</element-citation>
			</ref>
			<ref id="B3">
				<label>3</label>
				<mixed-citation>3. Tan W, Zhao X, Ma X, Wang W, Niu P, Xu W, <italic>et al</italic>. A Novel Coronavirus Genome Identified in a Cluster of Pneumonia Cases - Wuhan, China 2019-2020. China CDC Weekly. 2020;2(4):61-2. <ext-link ext-link-type="uri" xlink:href="https://doi.org/gg8z47">https://doi.org/gg8z47</ext-link>.</mixed-citation>
				<element-citation publication-type="journal">
					<person-group person-group-type="author">
						<name>
							<surname>Tan</surname>
							<given-names>W</given-names>
						</name>
						<name>
							<surname>Zhao</surname>
							<given-names>X</given-names>
						</name>
						<name>
							<surname>Ma</surname>
							<given-names>X</given-names>
						</name>
						<name>
							<surname>Wang</surname>
							<given-names>W</given-names>
						</name>
						<name>
							<surname>Niu</surname>
							<given-names>P</given-names>
						</name>
						<name>
							<surname>Xu</surname>
							<given-names>W</given-names>
						</name>
						<etal/>
					</person-group>
					<article-title>A Novel Coronavirus Genome Identified in a Cluster of Pneumonia Cases - Wuhan, China 2019-2020</article-title>
					<source>China CDC Weekly</source>
					<year>2020</year>
					<volume>2</volume>
					<issue>4</issue>
					<fpage>61</fpage>
					<lpage>62</lpage>
					<ext-link ext-link-type="uri" xlink:href="https://doi.org/gg8z47">https://doi.org/gg8z47</ext-link>
				</element-citation>
			</ref>
			<ref id="B4">
				<label>4</label>
				<mixed-citation>4. World Health Organization (WHO). Tracking SARS-CoV-2 variants. Geneva: WHO; 2021 [cited 2021 Jul 28]. Available from: <comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3uezo35">https://bit.ly/3uezo35</ext-link>
					</comment>.</mixed-citation>
				<element-citation publication-type="book">
					<person-group person-group-type="author">
						<collab>World Health Organization (WHO)</collab>
					</person-group>
					<source>Tracking SARS-CoV-2 variants</source>
					<publisher-loc>Geneva</publisher-loc>
					<publisher-name>WHO</publisher-name>
					<year>2021</year>
					<date-in-citation content-type="access-date" iso-8601-date="2021-00-00">2021 Jul 28</date-in-citation>
					<comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3uezo35">https://bit.ly/3uezo35</ext-link>
					</comment>
				</element-citation>
			</ref>
			<ref id="B5">
				<label>5</label>
				<mixed-citation>5. World Health Organization. Enfermedad por coronavirus (COVID-19): variantes del SARS-COV-2. Geneve: OMS; 2021.</mixed-citation>
				<element-citation publication-type="book">
					<person-group person-group-type="author">
						<collab>World Health Organization</collab>
					</person-group>
					<source>Enfermedad por coronavirus (COVID-19): variantes del SARS-COV-2</source>
					<publisher-loc>Geneve</publisher-loc>
					<publisher-name>OMS</publisher-name>
					<year>2021</year>
				</element-citation>
			</ref>
			<ref id="B6">
				<label>6</label>
				<mixed-citation>6. European Centre for Disease Prevention and Control (ECDC). Threat Assessment Brief: Implications for the EU/EEA on the spread of the SARS-CoV-2 Delta (B.1.617.2) variant of concern. Stockholm: ECDC; 2021 [cited 2021 Jul 28]. Available from: <comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3NC0h8d">https://bit.ly/3NC0h8d</ext-link>
					</comment>.</mixed-citation>
				<element-citation publication-type="book">
					<person-group person-group-type="author">
						<collab>European Centre for Disease Prevention and Control (ECDC)</collab>
					</person-group>
					<source>Threat Assessment Brief: Implications for the EU/EEA on the spread of the SARS-CoV-2 Delta (B.1.617.2) variant of concern. Stockholm: ECDC</source>
					<year>2021</year>
					<date-in-citation content-type="access-date" iso-8601-date="2021-00-00">2021 Jul 28</date-in-citation>
					<comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3NC0h8d">https://bit.ly/3NC0h8d</ext-link>
					</comment>
				</element-citation>
			</ref>
			<ref id="B7">
				<label>7</label>
				<mixed-citation>7. American Society for Microbiology (ASM). How Dangerous Is the Delta Variant (B.1.617.2)? Washington, DC: ASM; 2021.</mixed-citation>
				<element-citation publication-type="book">
					<person-group person-group-type="author">
						<collab>American Society for Microbiology (ASM)</collab>
					</person-group>
					<source>How Dangerous Is the Delta Variant (B.1.617.2)?</source>
					<publisher-loc>Washington, DC</publisher-loc>
					<publisher-name>ASM</publisher-name>
					<year>2021</year>
				</element-citation>
			</ref>
			<ref id="B8">
				<label>8</label>
				<mixed-citation>8. del Rio C, Malani PN, Omer SB. Confronting the Delta Variant of SARS-CoV-2, Summer 2021. JAMA. 2021;326(11):1001-2. <ext-link ext-link-type="uri" xlink:href="https://doi.org/gmzprd">https://doi.org/gmzprd</ext-link>.</mixed-citation>
				<element-citation publication-type="journal">
					<person-group person-group-type="author">
						<name>
							<surname>del Rio</surname>
							<given-names>C</given-names>
						</name>
						<name>
							<surname>Malani</surname>
							<given-names>PN</given-names>
						</name>
						<name>
							<surname>Omer</surname>
							<given-names>SB</given-names>
						</name>
					</person-group>
					<article-title>Confronting the Delta Variant of SARS-CoV-2, Summer 2021</article-title>
					<source>JAMA</source>
					<year>2021</year>
					<volume>326</volume>
					<issue>11</issue>
					<fpage>1001</fpage>
					<lpage>1002</lpage>
					<ext-link ext-link-type="uri" xlink:href="https://doi.org/gmzprd">https://doi.org/gmzprd</ext-link>
				</element-citation>
			</ref>
			<ref id="B9">
				<label>9</label>
				<mixed-citation>9. Riley S, Wang H, Eales O, Haw D, Walters CE, Ainslie KEC, <italic>et al</italic>. REACT-1 round 12 report: resurgence of SARS-CoV-2 infections in England associated with increased frequency of the Delta variant. medRxiv. 2021. <ext-link ext-link-type="uri" xlink:href="https://doi.org/h3x9">https://doi.org/h3x9</ext-link>.</mixed-citation>
				<element-citation publication-type="book">
					<person-group person-group-type="author">
						<name>
							<surname>Riley</surname>
							<given-names>S</given-names>
						</name>
						<name>
							<surname>Wang</surname>
							<given-names>H</given-names>
						</name>
						<name>
							<surname>Eales</surname>
							<given-names>O</given-names>
						</name>
						<name>
							<surname>Haw</surname>
							<given-names>D</given-names>
						</name>
						<name>
							<surname>Walters</surname>
							<given-names>CE</given-names>
						</name>
						<name>
							<surname>Ainslie</surname>
							<given-names>KEC</given-names>
						</name>
						<etal/>
					</person-group>
					<source>REACT-1 round 12 report: resurgence of SARS-CoV-2 infections in England associated with increased frequency of the Delta variant. medRxiv</source>
					<year>2021</year>
					<ext-link ext-link-type="uri" xlink:href="https://doi.org/h3x9">https://doi.org/h3x9</ext-link>
				</element-citation>
			</ref>
			<ref id="B10">
				<label>10</label>
				<mixed-citation>10. Planas D, Veyer D, Baidaliuk A, Staropoli I, Guivel-Benhassine F, Rajah MM, <italic>et al</italic>. Reduced sensitivity of SARS-CoV-2 variant Delta to antibody neutralization. Nature. 2021;596(7871):276-80. <ext-link ext-link-type="uri" xlink:href="https://doi.org/gk5m38">https://doi.org/gk5m38</ext-link>.</mixed-citation>
				<element-citation publication-type="journal">
					<person-group person-group-type="author">
						<name>
							<surname>Planas</surname>
							<given-names>D</given-names>
						</name>
						<name>
							<surname>Veyer</surname>
							<given-names>D</given-names>
						</name>
						<name>
							<surname>Baidaliuk</surname>
							<given-names>A</given-names>
						</name>
						<name>
							<surname>Staropoli</surname>
							<given-names>I</given-names>
						</name>
						<name>
							<surname>Guivel-Benhassine</surname>
							<given-names>F</given-names>
						</name>
						<name>
							<surname>Rajah</surname>
							<given-names>MM</given-names>
						</name>
						<etal/>
					</person-group>
					<article-title>Reduced sensitivity of SARS-CoV-2 variant Delta to antibody neutralization</article-title>
					<source>Nature</source>
					<year>2021</year>
					<volume>596</volume>
					<issue>7871</issue>
					<fpage>276</fpage>
					<lpage>280</lpage>
					<ext-link ext-link-type="uri" xlink:href="https://doi.org/gk5m38">https://doi.org/gk5m38</ext-link>
				</element-citation>
			</ref>
			<ref id="B11">
				<label>11</label>
				<mixed-citation>11. World Health Organization (WHO). COVID-19 weekly epidemiological update, edition 46, 29 Jun 2021. Geneve: WHO; 2021 [cited 2021 Jul 29]. Available from: <comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3BuPpqo">https://bit.ly/3BuPpqo</ext-link>
					</comment>.</mixed-citation>
				<element-citation publication-type="book">
					<person-group person-group-type="author">
						<collab>World Health Organization (WHO)</collab>
					</person-group>
					<source>COVID-19 weekly epidemiological update, edition 46, 29 Jun 2021</source>
					<publisher-loc>Geneve</publisher-loc>
					<publisher-name>WHO</publisher-name>
					<year>2021</year>
					<date-in-citation content-type="access-date" iso-8601-date="2021-00-00">2021 Jul 29</date-in-citation>
					<comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3BuPpqo">https://bit.ly/3BuPpqo</ext-link>
					</comment>
				</element-citation>
			</ref>
			<ref id="B12">
				<label>12</label>
				<mixed-citation>12. World Health Organization (WHO). COVID-19 weekly epidemiological update, edition 50, 27 Jul 2021. Geneva: WHO; 2021 [cited 2021 Jul 29]. Available from: <comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3OSZMr6">https://bit.ly/3OSZMr6</ext-link>
					</comment>.</mixed-citation>
				<element-citation publication-type="book">
					<person-group person-group-type="author">
						<collab>World Health Organization (WHO)</collab>
					</person-group>
					<source>COVID-19 weekly epidemiological update, edition 50, 27 Jul 2021</source>
					<publisher-loc>Geneva</publisher-loc>
					<publisher-name>WHO</publisher-name>
					<year>2021</year>
					<date-in-citation content-type="access-date" iso-8601-date="2021-00-00">2021 Jul 29</date-in-citation>
					<comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3OSZMr6">https://bit.ly/3OSZMr6</ext-link>
					</comment>
				</element-citation>
			</ref>
			<ref id="B13">
				<label>13</label>
				<mixed-citation>13. Cherian S, Potdar V, Jadhav S, Yadav P, Gupta N, Das M, <italic>et al</italic>. SARS-CoV-2 Spike Mutations, L452R, T478K, E484Q and P681R, in the Second Wave of COVID-19 in Maharashtra, India. Microorganisms. 2021;9(7):1542. <ext-link ext-link-type="uri" xlink:href="https://doi.org/gmkck4">https://doi.org/gmkck4</ext-link>.</mixed-citation>
				<element-citation publication-type="journal">
					<person-group person-group-type="author">
						<name>
							<surname>Cherian</surname>
							<given-names>S</given-names>
						</name>
						<name>
							<surname>Potdar</surname>
							<given-names>V</given-names>
						</name>
						<name>
							<surname>Jadhav</surname>
							<given-names>S</given-names>
						</name>
						<name>
							<surname>Yadav</surname>
							<given-names>P</given-names>
						</name>
						<name>
							<surname>Gupta</surname>
							<given-names>N</given-names>
						</name>
						<name>
							<surname>Das</surname>
							<given-names>M</given-names>
						</name>
						<etal/>
					</person-group>
					<article-title>SARS-CoV-2 Spike Mutations, L452R, T478K, E484Q and P681R, in the Second Wave of COVID-19 in Maharashtra, India</article-title>
					<source>Microorganisms</source>
					<year>2021</year>
					<volume>9</volume>
					<issue>7</issue>
					<fpage>1542</fpage>
					<lpage>1542</lpage>
					<ext-link ext-link-type="uri" xlink:href="https://doi.org/gmkck4">https://doi.org/gmkck4</ext-link>
				</element-citation>
			</ref>
			<ref id="B14">
				<label>14</label>
				<mixed-citation>14. Peacock TP, Sheppard CM, Brown JC, Goonawardane N, Zhou J, Whiteley M, <italic>et al</italic>. The SARS-CoV-2 variants associated with infections in India, B.1.617, show enhanced spike cleavage by furin. bioRxiv. 2021. <ext-link ext-link-type="uri" xlink:href="https://doi.org/h3zb">https://doi.org/h3zb</ext-link>.</mixed-citation>
				<element-citation publication-type="book">
					<person-group person-group-type="author">
						<name>
							<surname>Peacock</surname>
							<given-names>TP</given-names>
						</name>
						<name>
							<surname>Sheppard</surname>
							<given-names>CM</given-names>
						</name>
						<name>
							<surname>Brown</surname>
							<given-names>JC</given-names>
						</name>
						<name>
							<surname>Goonawardane</surname>
							<given-names>N</given-names>
						</name>
						<name>
							<surname>Zhou</surname>
							<given-names>J</given-names>
						</name>
						<name>
							<surname>Whiteley</surname>
							<given-names>M</given-names>
						</name>
						<etal/>
					</person-group>
					<source>The SARS-CoV-2 variants associated with infections in India, B.1.617, show enhanced spike cleavage by furin. bioRxiv</source>
					<year>2021</year>
					<ext-link ext-link-type="uri" xlink:href="https://doi.org/h3zb">https://doi.org/h3zb</ext-link>
				</element-citation>
			</ref>
			<ref id="B15">
				<label>15</label>
				<mixed-citation>15. Public Health England. SARS-CoV-2 variants of concern and variants under investigation in England. Technical briefing 18. Public Health England; 2021 [Cited 2021 July 29]. Available from: <comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3uezo35">https://bit.ly/3uezo35</ext-link>
					</comment>.</mixed-citation>
				<element-citation publication-type="book">
					<person-group person-group-type="author">
						<collab>Public Health England</collab>
					</person-group>
					<source>SARS-CoV-2 variants of concern and variants under investigation in England. Technical briefing 18</source>
					<publisher-name>Public Health England</publisher-name>
					<year>2021</year>
					<date-in-citation content-type="access-date" iso-8601-date="2021-00-00">2021 July </date-in-citation>
					<comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3uezo35">https://bit.ly/3uezo35</ext-link>
					</comment>
				</element-citation>
			</ref>
			<ref id="B16">
				<label>16</label>
				<mixed-citation>16. GOV.UK. Imperial College London: Evaluating the roadmap out of lockdown - modelling Step 4 of the roadmap in the context of B.1.617.2. London; 2021 [cited 2021 Jul 29]. Available from: <comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3abfvDs">https://bit.ly/3abfvDs</ext-link>
					</comment>.</mixed-citation>
				<element-citation publication-type="book">
					<person-group person-group-type="author">
						<collab>GOV.UK</collab>
					</person-group>
					<source>Imperial College London: Evaluating the roadmap out of lockdown - modelling Step 4 of the roadmap in the context of B.1.617.2</source>
					<publisher-loc>London</publisher-loc>
					<year>2021</year>
					<date-in-citation content-type="access-date" iso-8601-date="2021-00-00">2021 Jul 29</date-in-citation>
					<comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3abfvDs">https://bit.ly/3abfvDs</ext-link>
					</comment>
				</element-citation>
			</ref>
			<ref id="B17">
				<label>17</label>
				<mixed-citation>17. GOV.UK. SPI-M-O: Summary of further modelling of easing restrictions - roadmap Step 4, 9 June 2021. London; 2021 [cited 2021 Jul 29]. Available from: <comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3Ah8POR">https://bit.ly/3Ah8POR</ext-link>
					</comment>.</mixed-citation>
				<element-citation publication-type="book">
					<person-group person-group-type="author">
						<collab>GOV.UK</collab>
					</person-group>
					<source>SPI-M-O: Summary of further modelling of easing restrictions - roadmap Step 4, 9 June 2021</source>
					<publisher-loc>London</publisher-loc>
					<year>2021</year>
					<date-in-citation content-type="access-date" iso-8601-date="2021-00-00">2021 Jul 29</date-in-citation>
					<comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3Ah8POR">https://bit.ly/3Ah8POR</ext-link>
					</comment>
				</element-citation>
			</ref>
			<ref id="B18">
				<label>18</label>
				<mixed-citation>18. GOV.UK. University of Warwick: Road map scenarios and sensitivity - Step 4, 9 June 2021. London; 2021 [cited 2021 Jul 29]. Available from: <comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3OVGWQu">https://bit.ly/3OVGWQu</ext-link>
					</comment>.</mixed-citation>
				<element-citation publication-type="book">
					<person-group person-group-type="author">
						<collab>GOV.UK</collab>
					</person-group>
					<source>University of Warwick: Road map scenarios and sensitivity - Step 4, 9 June 2021</source>
					<publisher-loc>London</publisher-loc>
					<year>2021</year>
					<date-in-citation content-type="access-date" iso-8601-date="2021-00-00">2021 Jul 29</date-in-citation>
					<comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3OVGWQu">https://bit.ly/3OVGWQu</ext-link>
					</comment>
				</element-citation>
			</ref>
			<ref id="B19">
				<label>19</label>
				<mixed-citation>19. GOV.UK. LSHTM: Interim roadmap assessment - prior to Step 4, 9 June 2021. London; 2021 [cited 2021 Jul 29]. Available from: <comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3NCFIs7">https://bit.ly/3NCFIs7</ext-link>
					</comment>.</mixed-citation>
				<element-citation publication-type="book">
					<person-group person-group-type="author">
						<collab>GOV.UK</collab>
					</person-group>
					<source>LSHTM: Interim roadmap assessment - prior to Step 4, 9 June 2021</source>
					<publisher-loc>London</publisher-loc>
					<year>2021</year>
					<date-in-citation content-type="access-date" iso-8601-date="2021-00-00">2021 Jul 29</date-in-citation>
					<comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3NCFIs7">https://bit.ly/3NCFIs7</ext-link>
					</comment>
				</element-citation>
			</ref>
			<ref id="B20">
				<label>20</label>
				<mixed-citation>20. Campbell F, Archer B, Laurenson-Schafer H, Jinnai Y, Konings F, Batra N, <italic>et al</italic>. Increased transmissibility and global spread of SARS-CoV-2 variants of concern as at June 2021. Euro Surveill. 2021;26(24):2100509. <ext-link ext-link-type="uri" xlink:href="https://doi.org/gmkjw6">https://doi.org/gmkjw6</ext-link>.</mixed-citation>
				<element-citation publication-type="journal">
					<person-group person-group-type="author">
						<name>
							<surname>Campbell</surname>
							<given-names>F</given-names>
						</name>
						<name>
							<surname>Archer</surname>
							<given-names>B</given-names>
						</name>
						<name>
							<surname>Laurenson-Schafer</surname>
							<given-names>H</given-names>
						</name>
						<name>
							<surname>Jinnai</surname>
							<given-names>Y</given-names>
						</name>
						<name>
							<surname>Konings</surname>
							<given-names>F</given-names>
						</name>
						<name>
							<surname>Batra</surname>
							<given-names>N</given-names>
						</name>
						<etal/>
					</person-group>
					<article-title>Increased transmissibility and global spread of SARS-CoV-2 variants of concern as at June 2021</article-title>
					<source>Euro Surveill</source>
					<year>2021</year>
					<volume>26</volume>
					<issue>24</issue>
					<fpage>2100509</fpage>
					<lpage>2100509</lpage>
					<ext-link ext-link-type="uri" xlink:href="https://doi.org/gmkjw6">https://doi.org/gmkjw6</ext-link>
				</element-citation>
			</ref>
			<ref id="B21">
				<label>21</label>
				<mixed-citation>21. Mahase E. Delta variant: What is happening with transmission, hospital admissions, and restrictions? BMJ. 2021;373:n1513. <ext-link ext-link-type="uri" xlink:href="https://doi.org/gmkxxq">https://doi.org/gmkxxq</ext-link>.</mixed-citation>
				<element-citation publication-type="journal">
					<person-group person-group-type="author">
						<name>
							<surname>Mahase</surname>
							<given-names>E</given-names>
						</name>
					</person-group>
					<article-title>Delta variant: What is happening with transmission, hospital admissions, and restrictions?</article-title>
					<source>BMJ</source>
					<year>2021</year>
					<issue>373</issue>
					<fpage>n1513</fpage>
					<lpage>n1513</lpage>
					<ext-link ext-link-type="uri" xlink:href="https://doi.org/gmkxxq">https://doi.org/gmkxxq</ext-link>
				</element-citation>
			</ref>
			<ref id="B22">
				<label>22</label>
				<mixed-citation>22. Mackey K, Ayers CK, Kondo KK, Saha S, Advani SM, Young S, <italic>et al</italic>. Racial and Ethnic Disparities in COVID-19-Related Infections, Hospitalizations, and Deaths: A Systematic Review. Ann Intern Med. 2021;174(3):362-73. <ext-link ext-link-type="uri" xlink:href="https://doi.org/gkchjz">https://doi.org/gkchjz</ext-link>.</mixed-citation>
				<element-citation publication-type="journal">
					<person-group person-group-type="author">
						<name>
							<surname>Mackey</surname>
							<given-names>K</given-names>
						</name>
						<name>
							<surname>Ayers</surname>
							<given-names>CK</given-names>
						</name>
						<name>
							<surname>Kondo</surname>
							<given-names>KK</given-names>
						</name>
						<name>
							<surname>Saha</surname>
							<given-names>S</given-names>
						</name>
						<name>
							<surname>Advani</surname>
							<given-names>SM</given-names>
						</name>
						<name>
							<surname>Young</surname>
							<given-names>S</given-names>
						</name>
						<etal/>
					</person-group>
					<article-title>Racial and Ethnic Disparities in COVID-19-Related Infections, Hospitalizations, and Deaths: A Systematic Review</article-title>
					<source>Ann Intern Med</source>
					<year>2021</year>
					<volume>174</volume>
					<issue>3</issue>
					<fpage>362</fpage>
					<lpage>373</lpage>
					<ext-link ext-link-type="uri" xlink:href="https://doi.org/gkchjz">https://doi.org/gkchjz</ext-link>
				</element-citation>
			</ref>
			<ref id="B23">
				<label>23</label>
				<mixed-citation>23. Center for Disease Control and Prevention (CDC). COVID Data Tracker Weekly Review. Don't Run Down the Shot Clock. Clifton: CDC; 2021 [cited 2021 Jul 30]. Available from: <comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3OJfVjm">https://bit.ly/3OJfVjm</ext-link>
					</comment>.</mixed-citation>
				<element-citation publication-type="book">
					<person-group person-group-type="author">
						<collab>Center for Disease Control and Prevention (CDC)</collab>
					</person-group>
					<source>COVID Data Tracker Weekly Review. Don't Run Down the Shot Clock</source>
					<publisher-loc>Clifton</publisher-loc>
					<publisher-loc>CDC</publisher-loc>
					<year>2021</year>
					<date-in-citation content-type="access-date" iso-8601-date="2021-00-00">2021 Jul 30</date-in-citation>
					<comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3OJfVjm">https://bit.ly/3OJfVjm</ext-link>
					</comment>
				</element-citation>
			</ref>
			<ref id="B24">
				<label>24</label>
				<mixed-citation>24. Bolze A, Cirulli ET, Luo S, White S, Cassens T, Jacobs S, <italic>et al</italic>. Rapid displacement of SARS-CoV-2 variant B.1.1.7 by B.1.617.2 and P.1 in the United States. medRxiv. 2021.</mixed-citation>
				<element-citation publication-type="book">
					<person-group person-group-type="author">
						<name>
							<surname>Bolze</surname>
							<given-names>A</given-names>
						</name>
						<name>
							<surname>Cirulli</surname>
							<given-names>ET</given-names>
						</name>
						<name>
							<surname>Luo</surname>
							<given-names>S</given-names>
						</name>
						<name>
							<surname>White</surname>
							<given-names>S</given-names>
						</name>
						<name>
							<surname>Cassens</surname>
							<given-names>T</given-names>
						</name>
						<name>
							<surname>Jacobs</surname>
							<given-names>S</given-names>
						</name>
						<etal/>
					</person-group>
					<source>Rapid displacement of SARS-CoV-2 variant B.1.1.7 by B.1.617.2 and P.1 in the United States. medRxiv</source>
					<year>2021</year>
				</element-citation>
			</ref>
			<ref id="B25">
				<label>25</label>
				<mixed-citation>25. COVID infection &amp; vaccination rates in the UK today. ZOE Health Study. ZOE Limited; 2021 [cited 2021 Jul 27]. Available from: <comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3uf7yEc">https://bit.ly/3uf7yEc</ext-link>
					</comment>.</mixed-citation>
				<element-citation publication-type="book">
					<person-group person-group-type="author">
						<collab>COVID infection &amp; vaccination rates in the UK today</collab>
					</person-group>
					<source>ZOE Health Study</source>
					<publisher-name>ZOE Limited</publisher-name>
					<year>2021</year>
					<date-in-citation content-type="access-date" iso-8601-date="2021-00-00">2021 Jul 27</date-in-citation>
					<comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3uf7yEc">https://bit.ly/3uf7yEc</ext-link>
					</comment>
				</element-citation>
			</ref>
			<ref id="B26">
				<label>26</label>
				<mixed-citation>26. Sheikh A, McMenamin J, Taylor B, Robertson C. SARS-CoV-2 Delta VOC in Scotland: demographics, risk of hospital admission, and vaccine effectiveness. Lancet. 2021;397(10293):2461-2. <ext-link ext-link-type="uri" xlink:href="https://doi.org/gk4ht8">https://doi.org/gk4ht8</ext-link>.</mixed-citation>
				<element-citation publication-type="journal">
					<person-group person-group-type="author">
						<name>
							<surname>Sheikh</surname>
							<given-names>A</given-names>
						</name>
						<name>
							<surname>McMenamin</surname>
							<given-names>J</given-names>
						</name>
						<name>
							<surname>Taylor</surname>
							<given-names>B</given-names>
						</name>
						<name>
							<surname>Robertson</surname>
							<given-names>C</given-names>
						</name>
					</person-group>
					<article-title>SARS-CoV-2 Delta VOC in Scotland: demographics, risk of hospital admission, and vaccine effectiveness.</article-title>
					<source>Lancet</source>
					<year>2021</year>
					<volume>397</volume>
					<issue>10293</issue>
					<fpage>2461</fpage>
					<lpage>2462</lpage>
					<ext-link ext-link-type="uri" xlink:href="https://doi.org/gk4ht8">https://doi.org/gk4ht8</ext-link>
				</element-citation>
			</ref>
			<ref id="B27">
				<label>27</label>
				<mixed-citation>27. Public Health England. SARS-CoV-2 variants of concern and variants under investigation in England. Technical briefing 15. Public Health England; 2021 [Cited 2021 Jul 29]. Available from: <comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3QXdcVb">https://bit.ly/3QXdcVb</ext-link>
					</comment>.</mixed-citation>
				<element-citation publication-type="book">
					<person-group person-group-type="author">
						<collab>Public Health England</collab>
					</person-group>
					<source>SARS-CoV-2 variants of concern and variants under investigation in England. Technical briefing 15</source>
					<publisher-name>Public Health England</publisher-name>
					<year>2021</year>
					<date-in-citation content-type="access-date" iso-8601-date="2021-00-00">2021 Jul 29</date-in-citation>
					<comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3QXdcVb">https://bit.ly/3QXdcVb</ext-link>
					</comment>
				</element-citation>
			</ref>
			<ref id="B28">
				<label>28</label>
				<mixed-citation>28. European Centre for Disease Prevention and Control (ECDC). Implications for the EU/EEA on the spread of the SARS-CoV-2 Delta (B.1.617.2) variant of concern. Stockholm: ECDC; 2021 [cited 2021 Jul 27]. Available from: <comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3a4lNVy">https://bit.ly/3a4lNVy</ext-link>
					</comment>.</mixed-citation>
				<element-citation publication-type="book">
					<person-group person-group-type="author">
						<collab>European Centre for Disease Prevention and Control (ECDC)</collab>
					</person-group>
					<source>Implications for the EU/EEA on the spread of the SARS-CoV-2 Delta (B.1.617.2) variant of concern</source>
					<publisher-loc>Stockholm</publisher-loc>
					<publisher-name>ECDC</publisher-name>
					<year>2021</year>
					<date-in-citation content-type="access-date" iso-8601-date="2021-00-00">2021 Jul 27</date-in-citation>
					<comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3a4lNVy">https://bit.ly/3a4lNVy</ext-link>
					</comment>
				</element-citation>
			</ref>
			<ref id="B29">
				<label>29</label>
				<mixed-citation>29. Fisman DN, Tuite AR. Progressive Increase in Virulence of Novel SARS-CoV-2 Variants in Ontario, Canada. medRxiv. 2021. <ext-link ext-link-type="uri" xlink:href="https://doi.org/gmns9b">https://doi.org/gmns9b</ext-link>.</mixed-citation>
				<element-citation publication-type="book">
					<person-group person-group-type="author">
						<name>
							<surname>Fisman</surname>
							<given-names>DN</given-names>
						</name>
						<name>
							<surname>Tuite</surname>
							<given-names>AR</given-names>
						</name>
					</person-group>
					<source>Progressive Increase in Virulence of Novel SARS-CoV-2 Variants in Ontario, Canada. medRxiv</source>
					<year>2021</year>
					<ext-link ext-link-type="uri" xlink:href="https://doi.org/gmns9b">https://doi.org/gmns9b</ext-link>
				</element-citation>
			</ref>
			<ref id="B30">
				<label>30</label>
				<mixed-citation>30. Lopez-Bernal J, Andrews N, Gower C, Gallagher E, Simmons R, Thelwall S, <italic>et al</italic>. Effectiveness of COVID-19 vaccines against the B.1.617.2 (Delta) variant. N Engl J Med. 2021;385(7):585-94. <ext-link ext-link-type="uri" xlink:href="https://doi.org/gk8984">https://doi.org/gk8984</ext-link>.</mixed-citation>
				<element-citation publication-type="journal">
					<person-group person-group-type="author">
						<name>
							<surname>Lopez-Bernal</surname>
							<given-names>J</given-names>
						</name>
						<name>
							<surname>Andrews</surname>
							<given-names>N</given-names>
						</name>
						<name>
							<surname>Gower</surname>
							<given-names>C</given-names>
						</name>
						<name>
							<surname>Gallagher</surname>
							<given-names>E</given-names>
						</name>
						<name>
							<surname>Simmons</surname>
							<given-names>R</given-names>
						</name>
						<name>
							<surname>Thelwall</surname>
							<given-names>S</given-names>
						</name>
						<etal/>
					</person-group>
					<article-title>Effectiveness of COVID-19 vaccines against the B.1.617.2 (Delta) variant</article-title>
					<source>N Engl J Med</source>
					<year>2021</year>
					<volume>385</volume>
					<issue>7</issue>
					<fpage>585</fpage>
					<lpage>594</lpage>
					<ext-link ext-link-type="uri" xlink:href="https://doi.org/gk8984">https://doi.org/gk8984</ext-link>
				</element-citation>
			</ref>
			<ref id="B31">
				<label>31</label>
				<mixed-citation>31. Barouch DH, Stephenson KE, Sadoff J, Yu J, Chang A, Gebre M, <italic>et al</italic>. Durable Humoral and Cellular Immune Responses 8 Months after Ad26.COV2.S Vaccination. N Engl J Med. 2021;385(10):951-3. <ext-link ext-link-type="uri" xlink:href="https://doi.org/h379">https://doi.org/h379</ext-link>.</mixed-citation>
				<element-citation publication-type="journal">
					<person-group person-group-type="author">
						<name>
							<surname>Barouch</surname>
							<given-names>DH</given-names>
						</name>
						<name>
							<surname>Stephenson</surname>
							<given-names>KE</given-names>
						</name>
						<name>
							<surname>Sadoff</surname>
							<given-names>J</given-names>
						</name>
						<name>
							<surname>Yu</surname>
							<given-names>J</given-names>
						</name>
						<name>
							<surname>Chang</surname>
							<given-names>A</given-names>
						</name>
						<name>
							<surname>Gebre</surname>
							<given-names>M</given-names>
						</name>
						<etal/>
					</person-group>
					<article-title>Durable Humoral and Cellular Immune Responses 8 Months after Ad26.COV2.S Vaccination</article-title>
					<source>N Engl J Med</source>
					<year>2021</year>
					<volume>385</volume>
					<issue>10</issue>
					<fpage>951</fpage>
					<lpage>953</lpage>
					<ext-link ext-link-type="uri" xlink:href="https://doi.org/h379">https://doi.org/h379</ext-link>
				</element-citation>
			</ref>
			<ref id="B32">
				<label>32</label>
				<mixed-citation>32. Stowe J, Andrews N, Gower C, Gallagher E, Utsi L, Simmons R, <italic>et al</italic>. Effectiveness of COVID-19 vaccines against hospital admission with the Delta (B.1.617.2) variant. UK Health Security Agency [preprint]. 2021 [cited 2021 Jul 29]. Available from: <comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3uOgxwr">https://bit.ly/3uOgxwr</ext-link>
					</comment>.</mixed-citation>
				<element-citation publication-type="book">
					<person-group person-group-type="author">
						<name>
							<surname>Stowe</surname>
							<given-names>J</given-names>
						</name>
						<name>
							<surname>Andrews</surname>
							<given-names>N</given-names>
						</name>
						<name>
							<surname>Gower</surname>
							<given-names>C</given-names>
						</name>
						<name>
							<surname>Gallagher</surname>
							<given-names>E</given-names>
						</name>
						<name>
							<surname>Utsi</surname>
							<given-names>L</given-names>
						</name>
						<name>
							<surname>Simmons</surname>
							<given-names>R</given-names>
						</name>
						<etal/>
					</person-group>
					<source>Effectiveness of COVID-19 vaccines against hospital admission with the Delta (B.1.617.2) variant</source>
					<publisher-name>UK Health Security Agency</publisher-name>
					<year>2021</year>
					<date-in-citation content-type="access-date" iso-8601-date="2021-00-00">2021 Jul 29</date-in-citation>
					<comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3uOgxwr">https://bit.ly/3uOgxwr</ext-link>
					</comment>
				</element-citation>
			</ref>
			<ref id="B33">
				<label>33</label>
				<mixed-citation>33. Jongeneelen M, Kaszas K, Veldman D, Huizingh J, van der Vlugt R, Schouten T, <italic>et al</italic>. Ad26.COV2.S elicited neutralizing activity against Delta and other SARS-CoV-2 variants of concern. bioRxiv. 2021. <ext-link ext-link-type="uri" xlink:href="https://doi.org/gmns9g">https://doi.org/gmns9g</ext-link>.</mixed-citation>
				<element-citation publication-type="book">
					<person-group person-group-type="author">
						<name>
							<surname>Jongeneelen</surname>
							<given-names>M</given-names>
						</name>
						<name>
							<surname>Kaszas</surname>
							<given-names>K</given-names>
						</name>
						<name>
							<surname>Veldman</surname>
							<given-names>D</given-names>
						</name>
						<name>
							<surname>Huizingh</surname>
							<given-names>J</given-names>
						</name>
						<name>
							<surname>van der Vlugt</surname>
							<given-names>R</given-names>
						</name>
						<name>
							<surname>Schouten</surname>
							<given-names>T</given-names>
						</name>
						<etal/>
					</person-group>
					<source>Ad26.COV2.S elicited neutralizing activity against Delta and other SARS-CoV-2 variants of concern. bioRxiv</source>
					<year>2021</year>
					<ext-link ext-link-type="uri" xlink:href="https://doi.org/gmns9g">https://doi.org/gmns9g</ext-link>
				</element-citation>
			</ref>
			<ref id="B34">
				<label>34</label>
				<mixed-citation>34. Khoury DS, Cromer D, Reynaldi A, Schlub TE, Wheatley AK, Juno JA, <italic>et al</italic>. Neutralizing antibody levels are highly predictive of immune protection from symptomatic SARS-CoV-2 infection. Nat Med. 2021;27(7):1205-11. <ext-link ext-link-type="uri" xlink:href="https://doi.org/gj3h47">https://doi.org/gj3h47</ext-link>.</mixed-citation>
				<element-citation publication-type="journal">
					<person-group person-group-type="author">
						<name>
							<surname>Khoury</surname>
							<given-names>DS</given-names>
						</name>
						<name>
							<surname>Cromer</surname>
							<given-names>D</given-names>
						</name>
						<name>
							<surname>Reynaldi</surname>
							<given-names>A</given-names>
						</name>
						<name>
							<surname>Schlub</surname>
							<given-names>TE</given-names>
						</name>
						<name>
							<surname>Wheatley</surname>
							<given-names>AK</given-names>
						</name>
						<name>
							<surname>Juno</surname>
							<given-names>JA</given-names>
						</name>
						<etal/>
					</person-group>
					<article-title>Neutralizing antibody levels are highly predictive of immune protection from symptomatic SARS-CoV-2 infection</article-title>
					<source>Nat Med</source>
					<year>2021</year>
					<volume>27</volume>
					<issue>7</issue>
					<fpage>1205</fpage>
					<lpage>1211</lpage>
					<ext-link ext-link-type="uri" xlink:href="https://doi.org/gj3h47">https://doi.org/gj3h47</ext-link>
				</element-citation>
			</ref>
			<ref id="B35">
				<label>35</label>
				<mixed-citation>35. Moon MJ. Fighting COVID-19 with Agility, Transparency, and Participation: Wicked Policy Problems and New Governance Challenges. Public Adm Rev. 2020;80(4):651-6. <ext-link ext-link-type="uri" xlink:href="https://doi.org/ggwq7q">https://doi.org/ggwq7q</ext-link>.</mixed-citation>
				<element-citation publication-type="journal">
					<person-group person-group-type="author">
						<name>
							<surname>Moon</surname>
							<given-names>MJ</given-names>
						</name>
					</person-group>
					<article-title>Fighting COVID-19 with Agility, Transparency, and Participation: Wicked Policy Problems and New Governance Challenges</article-title>
					<source>Public Adm Rev</source>
					<year>2020</year>
					<volume>80</volume>
					<issue>4</issue>
					<fpage>651</fpage>
					<lpage>656</lpage>
					<ext-link ext-link-type="uri" xlink:href="https://doi.org/ggwq7q">https://doi.org/ggwq7q</ext-link>
				</element-citation>
			</ref>
			<ref id="B36">
				<label>36</label>
				<mixed-citation>36. Wu K, Werner AP, Koch M, Choi A, Narayanan E, Stewart-Jones GBE, et al. Serum Neutralizing Activity Elicited by mRNA-1273 Vaccine. N Engl J Med. 2021;384(15):1468-1470. <ext-link ext-link-type="uri" xlink:href="https://doi.org/gh4t34">https://doi.org/gh4t34</ext-link>.</mixed-citation>
				<element-citation publication-type="journal">
					<person-group person-group-type="author">
						<name>
							<surname>Wu</surname>
							<given-names>K</given-names>
						</name>
						<name>
							<surname>Werner</surname>
							<given-names>AP</given-names>
						</name>
						<name>
							<surname>Koch</surname>
							<given-names>M</given-names>
						</name>
						<name>
							<surname>Choi</surname>
							<given-names>A</given-names>
						</name>
						<name>
							<surname>Narayanan</surname>
							<given-names>E</given-names>
						</name>
						<name>
							<surname>Stewart-Jones</surname>
							<given-names>GBE</given-names>
						</name>
						<etal/>
					</person-group>
					<article-title>Serum Neutralizing Activity Elicited by mRNA-1273 Vaccine</article-title>
					<source>N Engl J Med</source>
					<year>2021</year>
					<volume>384</volume>
					<issue>15</issue>
					<fpage>1468</fpage>
					<lpage>1470</lpage>
					<ext-link ext-link-type="uri" xlink:href="https://doi.org/gh4t34">https://doi.org/gh4t34</ext-link>
				</element-citation>
			</ref>
			<ref id="B37">
				<label>37</label>
				<mixed-citation>37. Plotkin SA. Correlates of protection induced by vaccination. Clin Vaccine Immunol. 2010;17(7):1055-65. <ext-link ext-link-type="uri" xlink:href="https://doi.org/c5cs2q">https://doi.org/c5cs2q</ext-link>.</mixed-citation>
				<element-citation publication-type="journal">
					<person-group person-group-type="author">
						<name>
							<surname>Plotkin</surname>
							<given-names>SA</given-names>
						</name>
					</person-group>
					<article-title>Correlates of protection induced by vaccination</article-title>
					<source>Clin Vaccine Immunol</source>
					<year>2010</year>
					<volume>17</volume>
					<issue>7</issue>
					<fpage>1055</fpage>
					<lpage>1065</lpage>
					<ext-link ext-link-type="uri" xlink:href="https://doi.org/c5cs2q">https://doi.org/c5cs2q</ext-link>
				</element-citation>
			</ref>
			<ref id="B38">
				<label>38</label>
				<mixed-citation>38. Wall EC, Wu M, Harvey R, Kelly G, Warchal S, Sawyer C, <italic>et al</italic>. Neutralising antibody activity against SARS-CoV-2 VOCs B.1.617.2 and B.1.351 by BNT162b2 vaccination. Lancet. 2021;397(10292):2331-3. <ext-link ext-link-type="uri" xlink:href="https://doi.org/gkc8fs">https://doi.org/gkc8fs</ext-link>.</mixed-citation>
				<element-citation publication-type="journal">
					<person-group person-group-type="author">
						<name>
							<surname>Wall</surname>
							<given-names>EC</given-names>
						</name>
						<name>
							<surname>Wu</surname>
							<given-names>M</given-names>
						</name>
						<name>
							<surname>Harvey</surname>
							<given-names>R</given-names>
						</name>
						<name>
							<surname>Kelly</surname>
							<given-names>G</given-names>
						</name>
						<name>
							<surname>Warchal</surname>
							<given-names>S</given-names>
						</name>
						<name>
							<surname>Sawyer</surname>
							<given-names>C</given-names>
						</name>
						<etal/>
					</person-group>
					<article-title>Neutralising antibody activity against SARS-CoV-2 VOCs B.1.617.2 and B.1.351 by BNT162b2 vaccination</article-title>
					<source>Lancet</source>
					<year>2021</year>
					<volume>397</volume>
					<issue>10292</issue>
					<fpage>2331</fpage>
					<lpage>2333</lpage>
					<ext-link ext-link-type="uri" xlink:href="https://doi.org/gkc8fs">https://doi.org/gkc8fs</ext-link>
				</element-citation>
			</ref>
			<ref id="B39">
				<label>39</label>
				<mixed-citation>39. Tada T, Zhou H, Samanovic MI, Dcosta BM, Cornelius A, Mulligan MJ, <italic>et al</italic>. Comparison of Neutralizing Antibody Titers Elicited by mRNA and Adenoviral Vector Vaccine against SARS-CoV-2 Variants. bioRxiv. 2021. <ext-link ext-link-type="uri" xlink:href="https://doi.org/gk858j">https://doi.org/gk858j</ext-link>.</mixed-citation>
				<element-citation publication-type="book">
					<person-group person-group-type="author">
						<name>
							<surname>Tada</surname>
							<given-names>T</given-names>
						</name>
						<name>
							<surname>Zhou</surname>
							<given-names>H</given-names>
						</name>
						<name>
							<surname>Samanovic</surname>
							<given-names>MI</given-names>
						</name>
						<name>
							<surname>Dcosta</surname>
							<given-names>BM</given-names>
						</name>
						<name>
							<surname>Cornelius</surname>
							<given-names>A</given-names>
						</name>
						<name>
							<surname>Mulligan</surname>
							<given-names>MJ</given-names>
						</name>
						<etal/>
					</person-group>
					<source>Comparison of Neutralizing Antibody Titers Elicited by mRNA and Adenoviral Vector Vaccine against SARS-CoV-2 Variants. bioRxiv</source>
					<year>2021</year>
					<ext-link ext-link-type="uri" xlink:href="https://doi.org/gk858j">https://doi.org/gk858j</ext-link>
				</element-citation>
			</ref>
			<ref id="B40">
				<label>40</label>
				<mixed-citation>40. Choi A, Koch M, Wu K, Dixon G, Oestreicher J, Legault H, <italic>et al</italic>. Serum Neutralizing Activity of mRNA-1273 against SARS-CoV-2 Variants. bioRxiv. 2021. <ext-link ext-link-type="uri" xlink:href="https://doi.org/gmns9q">https://doi.org/gmns9q</ext-link>.</mixed-citation>
				<element-citation publication-type="book">
					<person-group person-group-type="author">
						<name>
							<surname>Choi</surname>
							<given-names>A</given-names>
						</name>
						<name>
							<surname>Koch</surname>
							<given-names>M</given-names>
						</name>
						<name>
							<surname>Wu</surname>
							<given-names>K</given-names>
						</name>
						<name>
							<surname>Dixon</surname>
							<given-names>G</given-names>
						</name>
						<name>
							<surname>Oestreicher</surname>
							<given-names>J</given-names>
						</name>
						<name>
							<surname>Legault</surname>
							<given-names>H</given-names>
						</name>
						<etal/>
					</person-group>
					<source>Serum Neutralizing Activity of mRNA-1273 against SARS-CoV-2 Variants. bioRxiv</source>
					<year>2021</year>
					<ext-link ext-link-type="uri" xlink:href="https://doi.org/gmns9q">https://doi.org/gmns9q</ext-link>
				</element-citation>
			</ref>
			<ref id="B41">
				<label>41</label>
				<mixed-citation>41. Saito A, Irie T, Suzuki R, Maemura T, Nasser H, Uriu K, <italic>et al</italic>. SARS-CoV-2 spike P681R mutation, a hallmark of the Delta variant, enhances viral fusogenicity and pathogenicity. bioRxiv. 2021. <ext-link ext-link-type="uri" xlink:href="https://doi.org/gk7d6w">https://doi.org/gk7d6w</ext-link>.</mixed-citation>
				<element-citation publication-type="book">
					<person-group person-group-type="author">
						<name>
							<surname>Saito</surname>
							<given-names>A</given-names>
						</name>
						<name>
							<surname>Irie</surname>
							<given-names>T</given-names>
						</name>
						<name>
							<surname>Suzuki</surname>
							<given-names>R</given-names>
						</name>
						<name>
							<surname>Maemura</surname>
							<given-names>T</given-names>
						</name>
						<name>
							<surname>Nasser</surname>
							<given-names>H</given-names>
						</name>
						<name>
							<surname>Uriu</surname>
							<given-names>K</given-names>
						</name>
						<etal/>
					</person-group>
					<source>SARS-CoV-2 spike P681R mutation, a hallmark of the Delta variant, enhances viral fusogenicity and pathogenicity. bioRxiv</source>
					<year>2021</year>
					<ext-link ext-link-type="uri" xlink:href="https://doi.org/gk7d6w">https://doi.org/gk7d6w</ext-link>
				</element-citation>
			</ref>
			<ref id="B42">
				<label>42</label>
				<mixed-citation>42. Li B, Deng A, Li K, Hu Y, Li Z, Xiong Q, <italic>et al</italic>. Viral infection and transmission in a large, well-traced outbreak caused by the SARS-CoV-2 Delta variant. medRxiv. 2021. <ext-link ext-link-type="uri" xlink:href="https://doi.org/gk78tn">https://doi.org/gk78tn</ext-link>.</mixed-citation>
				<element-citation publication-type="book">
					<person-group person-group-type="author">
						<name>
							<surname>Li</surname>
							<given-names>B</given-names>
						</name>
						<name>
							<surname>Deng</surname>
							<given-names>A</given-names>
						</name>
						<name>
							<surname>Li</surname>
							<given-names>K</given-names>
						</name>
						<name>
							<surname>Hu</surname>
							<given-names>Y</given-names>
						</name>
						<name>
							<surname>Li</surname>
							<given-names>Z</given-names>
						</name>
						<name>
							<surname>Xiong</surname>
							<given-names>Q</given-names>
						</name>
						<etal/>
					</person-group>
					<source>Viral infection and transmission in a large, well-traced outbreak caused by the SARS-CoV-2 Delta variant. medRxiv</source>
					<year>2021</year>
					<ext-link ext-link-type="uri" xlink:href="https://doi.org/gk78tn">https://doi.org/gk78tn</ext-link>
				</element-citation>
			</ref>
			<ref id="B43">
				<label>43</label>
				<mixed-citation>43. Brown CM, Vostok J, Johnson H, Burns M, Gharpure R, Sami S, <italic>et al</italic>. Outbreak of SARS-CoV-2 Infections, Including COVID-19 Vaccine Breakthrough Infections, Associated with Large Public Gatherings- Barnstable County, Massachusetts, July 2021. MMMWR Morb Mortal Wkly Rep. 2021;70:1059-62. <ext-link ext-link-type="uri" xlink:href="https://doi.org/gmcq7m">https://doi.org/gmcq7m</ext-link>.</mixed-citation>
				<element-citation publication-type="journal">
					<person-group person-group-type="author">
						<name>
							<surname>Brown</surname>
							<given-names>CM</given-names>
						</name>
						<name>
							<surname>Vostok</surname>
							<given-names>J</given-names>
						</name>
						<name>
							<surname>Johnson</surname>
							<given-names>H</given-names>
						</name>
						<name>
							<surname>Burns</surname>
							<given-names>M</given-names>
						</name>
						<name>
							<surname>Gharpure</surname>
							<given-names>R</given-names>
						</name>
						<name>
							<surname>Sami</surname>
							<given-names>S</given-names>
						</name>
						<etal/>
					</person-group>
					<article-title>Outbreak of SARS-CoV-2 Infections, Including COVID-19 Vaccine Breakthrough Infections, Associated with Large Public Gatherings- Barnstable County, Massachusetts, July 2021</article-title>
					<source>MMMWR Morb Mortal Wkly Rep</source>
					<year>2021</year>
					<issue>70</issue>
					<fpage>1059</fpage>
					<lpage>1062</lpage>
					<ext-link ext-link-type="uri" xlink:href="https://doi.org/gmcq7m">https://doi.org/gmcq7m</ext-link>
				</element-citation>
			</ref>
			<ref id="B44">
				<label>44</label>
				<mixed-citation>44. European Centre for Disease Prevention and Control (ECDC). Guidelines for the implementation of non-pharmaceutical interventions against COVID-19. Stockholm: ECDC ; 2021 [cited 2021 Jul 29]. Available from: <comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3usMIRA">https://bit.ly/3usMIRA</ext-link>
					</comment>.</mixed-citation>
				<element-citation publication-type="book">
					<person-group person-group-type="author">
						<collab>European Centre for Disease Prevention and Control (ECDC)</collab>
					</person-group>
					<source>Guidelines for the implementation of non-pharmaceutical interventions against COVID-19</source>
					<publisher-loc>Stockholm</publisher-loc>
					<publisher-name>ECDC</publisher-name>
					<year>2021</year>
					<date-in-citation content-type="access-date" iso-8601-date="2021-00-00">2021 Jul 29</date-in-citation>
					<comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3usMIRA">https://bit.ly/3usMIRA</ext-link>
					</comment>
				</element-citation>
			</ref>
			<ref id="B45">
				<label>45</label>
				<mixed-citation>45. European Centre for Disease Prevention and Control (ECDC). COVID-19 Vaccine Tracker. Stockholm: ECDC ; 2021 [cited 2021 Jul 28]. Available from: <comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3Rd82Ev">https://bit.ly/3Rd82Ev</ext-link>
					</comment>.</mixed-citation>
				<element-citation publication-type="book">
					<person-group person-group-type="author">
						<collab>European Centre for Disease Prevention and Control (ECDC)</collab>
					</person-group>
					<source>COVID-19 Vaccine Tracker</source>
					<publisher-loc>Stockholm</publisher-loc>
					<publisher-name>ECDC</publisher-name>
					<year>2021</year>
					<date-in-citation content-type="access-date" iso-8601-date="2021-00-00">2021 Jul 28</date-in-citation>
					<comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3Rd82Ev">https://bit.ly/3Rd82Ev</ext-link>
					</comment>
				</element-citation>
			</ref>
			<ref id="B46">
				<label>46</label>
				<mixed-citation>46. European Centre for Disease Prevention and Control (ECDC). Operational tool on rapid risk assessment methodology - ECDC 2019. Stockholm: ECDC ; 2021 [cited 2021 Jul 29]. Available from: <comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3bNXwn0">https://bit.ly/3bNXwn0</ext-link>
					</comment>.</mixed-citation>
				<element-citation publication-type="book">
					<person-group person-group-type="author">
						<collab>European Centre for Disease Prevention and Control (ECDC)</collab>
					</person-group>
					<source>Operational tool on rapid risk assessment methodology - ECDC 2019</source>
					<publisher-loc>Stockholm</publisher-loc>
					<publisher-name>ECDC</publisher-name>
					<year>2021</year>
					<date-in-citation content-type="access-date" iso-8601-date="2021-00-00">2021 Jul 29</date-in-citation>
					<comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3bNXwn0">https://bit.ly/3bNXwn0</ext-link>
					</comment>
				</element-citation>
			</ref>
			<ref id="B47">
				<label>47</label>
				<mixed-citation>47. GOV.UK. Investigation of SARS-CoV-2 variants of concern: technical briefings. London; 2021 [cited 2021 Jul 28]. Available from: <comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3yInKjK">https://bit.ly/3yInKjK</ext-link>
					</comment>.</mixed-citation>
				<element-citation publication-type="book">
					<person-group person-group-type="author">
						<collab>GOV.UK</collab>
					</person-group>
					<source>Investigation of SARS-CoV-2 variants of concern: technical briefings</source>
					<publisher-loc>London</publisher-loc>
					<year>2021</year>
					<date-in-citation content-type="access-date" iso-8601-date="2021-00-00">2021 Jul 28</date-in-citation>
					<comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3yInKjK">https://bit.ly/3yInKjK</ext-link>
					</comment>
				</element-citation>
			</ref>
			<ref id="B48">
				<label>48</label>
				<mixed-citation>48. European Centre for Disease Prevention and Control (ECDC). The Response Measures Database (RMD). Stockholm: ECDC ; 2021 [cited 2021 Jul 28]. Available from: <comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3Ij0oV9">https://bit.ly/3Ij0oV9</ext-link>
					</comment>.</mixed-citation>
				<element-citation publication-type="book">
					<person-group person-group-type="author">
						<collab>European Centre for Disease Prevention and Control (ECDC)</collab>
					</person-group>
					<source>The Response Measures Database (RMD)</source>
					<publisher-loc>Stockholm</publisher-loc>
					<publisher-name>ECDC</publisher-name>
					<year>2021</year>
					<date-in-citation content-type="access-date" iso-8601-date="2021-00-00">2021 Jul 28</date-in-citation>
					<comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3Ij0oV9">https://bit.ly/3Ij0oV9</ext-link>
					</comment>
				</element-citation>
			</ref>
			<ref id="B49">
				<label>49</label>
				<mixed-citation>49. European Commission. Response Measures Database (RMD). 2021 [cited 2021 Jul 28]. Available from: <comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3IoQFg8">https://bit.ly/3IoQFg8</ext-link>
					</comment>.</mixed-citation>
				<element-citation publication-type="book">
					<person-group person-group-type="author">
						<collab>European Commission</collab>
					</person-group>
					<source>Response Measures Database (RMD)</source>
					<year>2021</year>
					<date-in-citation content-type="access-date" iso-8601-date="2021-00-00">2021 Jul 28</date-in-citation>
					<comment>Available from: <ext-link ext-link-type="uri" xlink:href="https://bit.ly/3IoQFg8">https://bit.ly/3IoQFg8</ext-link>
					</comment>
				</element-citation>
			</ref>
			<ref id="B50">
				<label>50</label>
				<mixed-citation>50. Baker MG, Wilson N, Blakely T. Elimination could be the optimal response strategy for covid-19 and other emerging pandemic diseases. BMJ. 2020;371:m4907. <ext-link ext-link-type="uri" xlink:href="https://doi.org/ghqk9h">https://doi.org/ghqk9h</ext-link>.</mixed-citation>
				<element-citation publication-type="journal">
					<person-group person-group-type="author">
						<name>
							<surname>Baker</surname>
							<given-names>MG</given-names>
						</name>
						<name>
							<surname>Wilson</surname>
							<given-names>N</given-names>
						</name>
						<name>
							<surname>Blakely</surname>
							<given-names>T</given-names>
						</name>
					</person-group>
					<article-title>Elimination could be the optimal response strategy for covid-19 and other emerging pandemic diseases</article-title>
					<source>BMJ</source>
					<year>2020</year>
					<issue>371</issue>
					<fpage>m4907</fpage>
					<lpage>m4907</lpage>
					<ext-link ext-link-type="uri" xlink:href="https://doi.org/ghqk9h">https://doi.org/ghqk9h</ext-link>
				</element-citation>
			</ref>
			<ref id="B51">
				<label>51</label>
				<mixed-citation>51. Oliu-Barton M, Pradelski BSR, Aghion P, Artus P, Kickbusch I, Lazarus JV, <italic>et al</italic>. SARS-CoV-2 elimination, not mitigation, creates best outcomes for health, the economy, and civil liberties. Lancet. 2021;397(10291):2234-6. <ext-link ext-link-type="uri" xlink:href="https://doi.org/f89p">https://doi.org/f89p</ext-link>.</mixed-citation>
				<element-citation publication-type="journal">
					<person-group person-group-type="author">
						<name>
							<surname>Oliu-Barton</surname>
							<given-names>M</given-names>
						</name>
						<name>
							<surname>Pradelski</surname>
							<given-names>BSR</given-names>
						</name>
						<name>
							<surname>Aghion</surname>
							<given-names>P</given-names>
						</name>
						<name>
							<surname>Artus</surname>
							<given-names>P</given-names>
						</name>
						<name>
							<surname>Kickbusch</surname>
							<given-names>I</given-names>
						</name>
						<name>
							<surname>Lazarus</surname>
							<given-names>JV</given-names>
						</name>
						<etal/>
					</person-group>
					<article-title>SARS-CoV-2 elimination, not mitigation, creates best outcomes for health, the economy, and civil liberties</article-title>
					<source>Lancet</source>
					<year>2021</year>
					<volume>397</volume>
					<issue>10291</issue>
					<fpage>2234</fpage>
					<lpage>2236</lpage>
					<ext-link ext-link-type="uri" xlink:href="https://doi.org/f89p">https://doi.org/f89p</ext-link>
				</element-citation>
			</ref>
			<ref id="B52">
				<label>52</label>
				<mixed-citation>52. Lazarus J. Las nuevas variantes de COVID-19 han cambiado las reglas del juego y no bastará con las vacunas. Necesitamos &quot;máxima supresión&quot; global. Barcelona: Instituto de Salud Global Barcelona; 2021.</mixed-citation>
				<element-citation publication-type="book">
					<person-group person-group-type="author">
						<name>
							<surname>Lazarus</surname>
							<given-names>J</given-names>
						</name>
					</person-group>
					<source>Las nuevas variantes de COVID-19 han cambiado las reglas del juego y no bastará con las vacunas. Necesitamos &quot;máxima supresión&quot; global</source>
					<publisher-loc>Barcelona</publisher-loc>
					<publisher-name>Instituto de Salud Global Barcelona</publisher-name>
					<year>2021</year>
				</element-citation>
			</ref>
			<ref id="B53">
				<label>53</label>
				<mixed-citation>53. Angeli F, Camporesi S, Dal Fabbro G. The COVID-19 wicked problem in public health ethics: conflicting evidence, or incommensurable values? Humanit Soc Sci Commun. 2021;8(161). <ext-link ext-link-type="uri" xlink:href="https://doi.org/h38q">https://doi.org/h38q</ext-link>.</mixed-citation>
				<element-citation publication-type="journal">
					<person-group person-group-type="author">
						<name>
							<surname>Angeli</surname>
							<given-names>F</given-names>
						</name>
						<name>
							<surname>Camporesi</surname>
							<given-names>S</given-names>
						</name>
						<name>
							<surname>Dal Fabbro</surname>
							<given-names>G</given-names>
						</name>
					</person-group>
					<article-title>The COVID-19 wicked problem in public health ethics: conflicting evidence, or incommensurable values?</article-title>
					<source>Humanit Soc Sci Commun</source>
					<year>2021</year>
					<volume>8</volume>
					<issue>161</issue>
					<ext-link ext-link-type="uri" xlink:href="https://doi.org/h38q">https://doi.org/h38q</ext-link>
				</element-citation>
			</ref>
			<ref id="B54">
				<label>54</label>
				<mixed-citation>54. Camporesi S, Mori M. Ethicists, doctors and triage decisions: who should decide? And on what basis? J Med Ethics. 2020;47(12):e18. <ext-link ext-link-type="uri" xlink:href="https://doi.org/gg4r4n">https://doi.org/gg4r4n</ext-link>.</mixed-citation>
				<element-citation publication-type="journal">
					<person-group person-group-type="author">
						<name>
							<surname>Camporesi</surname>
							<given-names>S</given-names>
						</name>
						<name>
							<surname>Mori</surname>
							<given-names>M</given-names>
						</name>
					</person-group>
					<article-title>Ethicists, doctors and triage decisions: who should decide? And on what basis?</article-title>
					<source>J Med Ethics</source>
					<year>2020</year>
					<volume>47</volume>
					<issue>12</issue>
					<elocation-id>e18</elocation-id>
					<ext-link ext-link-type="uri" xlink:href="https://doi.org/gg4r4n">https://doi.org/gg4r4n</ext-link>
				</element-citation>
			</ref>
			<ref id="B55">
				<label>55</label>
				<mixed-citation>55. Camporesi S. It Didn't Have to be This Way Reflections on the Ethical Justification of the Running Ban in Northern Italy in Response to the 2020 COVID-19 Outbreak. J Bioeth Inq. 2020;17(4):643-8. <ext-link ext-link-type="uri" xlink:href="https://doi.org/h38s">https://doi.org/h38s</ext-link>.</mixed-citation>
				<element-citation publication-type="journal">
					<person-group person-group-type="author">
						<name>
							<surname>Camporesi</surname>
							<given-names>S</given-names>
						</name>
					</person-group>
					<article-title>It Didn't Have to be This Way Reflections on the Ethical Justification of the Running Ban in Northern Italy in Response to the 2020 COVID-19 Outbreak</article-title>
					<source>J Bioeth Inq</source>
					<year>2020</year>
					<volume>17</volume>
					<issue>4</issue>
					<fpage>643</fpage>
					<lpage>648</lpage>
					<ext-link ext-link-type="uri" xlink:href="https://doi.org/h38s">https://doi.org/h38s</ext-link>
				</element-citation>
			</ref>
			<ref id="B56">
				<label>56</label>
				<mixed-citation>56. Rittel HWJ, Webber MM. Dilemmas in a general theory of planning. Policy Sci. 1973;4:155-69. <ext-link ext-link-type="uri" xlink:href="https://doi.org/c8mscz">https://doi.org/c8mscz</ext-link>.</mixed-citation>
				<element-citation publication-type="journal">
					<person-group person-group-type="author">
						<name>
							<surname>Rittel</surname>
							<given-names>HWJ</given-names>
						</name>
						<name>
							<surname>Webber</surname>
							<given-names>MM</given-names>
						</name>
					</person-group>
					<article-title>Dilemmas in a general theory of planning</article-title>
					<source>Policy Sci</source>
					<year>1973</year>
					<issue>4</issue>
					<fpage>155</fpage>
					<lpage>169</lpage>
					<ext-link ext-link-type="uri" xlink:href="https://doi.org/c8mscz">https://doi.org/c8mscz</ext-link>
				</element-citation>
			</ref>
		</ref-list>
		<fn-group>
			<fn fn-type="other" id="fn1">
				<label>How to cite:</label>
				<p> Yomayusa N, Vega R, Restre-po-Henao A, Morón L, Vaca C, Onate J. Delta variant of SARS-CoV-2: characteristics and implications for public health in Colombia. Rev. Fac. Med. 2022;70(1):e97460. English. doi: <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.15446/revfacmed.v70n1.97560">https://doi.org/10.15446/revfacmed.v70n1.97560</ext-link>.</p>
			</fn>
			<fn fn-type="other" id="fn2">
				<label>Cómo citar:</label>
				<p> Yomayusa N, Vega R, Restrepo-Henao A, Morón L, Vaca C, Onate J. [La variante Delta del SARS-CoV-2: características e implicaciones para la salud pública en Colombia]. Rev. Fac. Med. 2022;70(1):e97460. English. doi: <ext-link ext-link-type="uri" xlink:href="https://doi.org/10.15446/revfacmed.v70n1.97560">https://doi.org/10.15446/revfacmed.v70n1.97560</ext-link>.</p>
			</fn>
		</fn-group>
		<fn-group>
			<fn fn-type="financial-disclosure" id="fn4">
				<label>Funding</label>
				<p> None stated by the authors.</p>
			</fn>
		</fn-group>
	</back>
</article>