Clinical and Genomic Characterization of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS CoV-2) Infections in mRNA Vaccinated Health Care Personnel in New York City
Abstract Background Vaccine-induced clinical protection against severe acute respiratory syndrome coronavirus 2 (SARS CoV-2) variants is an evolving target. There are limited genomic level data on SARS CoV-2 breakthrough infections and vaccine effectiveness (VE) since the global spread of the B.1.61...
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creator | Robilotti, Elizabeth V Whiting, Karissa Lucca, Anabella Poon, Chester Guest, Rebecca McMillen, Tracy Jani, Krupa Solovyov, Alexander Kelson, Suzanne Browne, Kevin Freeswick, Scott Hohl, Tobias M Korenstein, Deborah Ruchnewitz, Denis Lässig, Michael Łuksza, Marta Greenbaum, Benjamin Seshan, Venkatraman E Esther Babady, N Kamboj, Mini |
description | Abstract
Background
Vaccine-induced clinical protection against severe acute respiratory syndrome coronavirus 2 (SARS CoV-2) variants is an evolving target. There are limited genomic level data on SARS CoV-2 breakthrough infections and vaccine effectiveness (VE) since the global spread of the B.1.617.2 (Delta) variant.
Methods
In a retrospective study from 1 November 2020 to 31 August 2021, divided as pre-Delta and Delta-dominant periods, laboratory-confirmed SARS CoV-2 infections among healthcare personnel (HCP) at a large tertiary cancer center in New York City were examined to compare the weekly infection rate-ratio in vaccinated, partially vaccinated, and unvaccinated HCP. We describe the clinical and genomic epidemiologic features of post-vaccine infections to assess for selection of variants of concern (VOC)/variants of interest (VOI) in the early post-vaccine period and impact of B.1.617.2 (Delta) variant domination on VE.
Results
Among 13658 HCP in our cohort, 12379 received at least 1 dose of a messenger RNA (mRNA) vaccine. In the pre-Delta period overall VE was 94.5%. Whole genome sequencing (WGS) of 369 isolates in the pre-Delta period did not reveal a clade bias for VOC/VOI specific to post-vaccine infections. VE in the Delta dominant phase was 75.6%. No hospitalizations occurred among vaccinated HCP in the entire study period, compared to 17 hospitalizations and 1 death among unvaccinated HCP.
Conclusions
Findings show high VE among HCP in New York City in the pre-Delta phase, with moderate decline in VE post-Delta emergence. SARS CoV-2 clades were similarly distributed among vaccinated and unvaccinated infected HCP without apparent clustering during the pre-Delta period of diverse clade circulation. Strong vaccine protection against hospitalization was maintained through the entire study period.
study of >13000 healthcare personnel (HCP) showed that messenger RNA (mRNA) vaccine effectiveness (VE) against coronavirus disease 2019 (COVID-19) was 94% through initial 5 months of follow-up, with moderate VE reduction to 75% during subsequent Delta-dominant period. No hospitalizations occurred among vaccinated HCP throughout the study period. |
doi_str_mv | 10.1093/cid/ciab886 |
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Background
Vaccine-induced clinical protection against severe acute respiratory syndrome coronavirus 2 (SARS CoV-2) variants is an evolving target. There are limited genomic level data on SARS CoV-2 breakthrough infections and vaccine effectiveness (VE) since the global spread of the B.1.617.2 (Delta) variant.
Methods
In a retrospective study from 1 November 2020 to 31 August 2021, divided as pre-Delta and Delta-dominant periods, laboratory-confirmed SARS CoV-2 infections among healthcare personnel (HCP) at a large tertiary cancer center in New York City were examined to compare the weekly infection rate-ratio in vaccinated, partially vaccinated, and unvaccinated HCP. We describe the clinical and genomic epidemiologic features of post-vaccine infections to assess for selection of variants of concern (VOC)/variants of interest (VOI) in the early post-vaccine period and impact of B.1.617.2 (Delta) variant domination on VE.
Results
Among 13658 HCP in our cohort, 12379 received at least 1 dose of a messenger RNA (mRNA) vaccine. In the pre-Delta period overall VE was 94.5%. Whole genome sequencing (WGS) of 369 isolates in the pre-Delta period did not reveal a clade bias for VOC/VOI specific to post-vaccine infections. VE in the Delta dominant phase was 75.6%. No hospitalizations occurred among vaccinated HCP in the entire study period, compared to 17 hospitalizations and 1 death among unvaccinated HCP.
Conclusions
Findings show high VE among HCP in New York City in the pre-Delta phase, with moderate decline in VE post-Delta emergence. SARS CoV-2 clades were similarly distributed among vaccinated and unvaccinated infected HCP without apparent clustering during the pre-Delta period of diverse clade circulation. Strong vaccine protection against hospitalization was maintained through the entire study period.
study of >13000 healthcare personnel (HCP) showed that messenger RNA (mRNA) vaccine effectiveness (VE) against coronavirus disease 2019 (COVID-19) was 94% through initial 5 months of follow-up, with moderate VE reduction to 75% during subsequent Delta-dominant period. No hospitalizations occurred among vaccinated HCP throughout the study period.</description><identifier>ISSN: 1058-4838</identifier><identifier>EISSN: 1537-6591</identifier><identifier>DOI: 10.1093/cid/ciab886</identifier><identifier>PMID: 34644393</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><subject>COVID-19 - epidemiology ; COVID-19 - prevention & control ; Delivery of Health Care ; Genomics ; Humans ; Major ; New York City - epidemiology ; Retrospective Studies ; RNA, Messenger ; SARS-CoV-2 - genetics</subject><ispartof>Clinical infectious diseases, 2022-08, Vol.75 (1), p.e774-e782</ispartof><rights>The Author(s) 2021. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com. 2021</rights><rights>The Author(s) 2021. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c412t-b663234397faafcc2e95d4ba775ee5e14a9a593211597c98f2728cd83ba445683</citedby><cites>FETCH-LOGICAL-c412t-b663234397faafcc2e95d4ba775ee5e14a9a593211597c98f2728cd83ba445683</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,1578,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34644393$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Robilotti, Elizabeth V</creatorcontrib><creatorcontrib>Whiting, Karissa</creatorcontrib><creatorcontrib>Lucca, Anabella</creatorcontrib><creatorcontrib>Poon, Chester</creatorcontrib><creatorcontrib>Guest, Rebecca</creatorcontrib><creatorcontrib>McMillen, Tracy</creatorcontrib><creatorcontrib>Jani, Krupa</creatorcontrib><creatorcontrib>Solovyov, Alexander</creatorcontrib><creatorcontrib>Kelson, Suzanne</creatorcontrib><creatorcontrib>Browne, Kevin</creatorcontrib><creatorcontrib>Freeswick, Scott</creatorcontrib><creatorcontrib>Hohl, Tobias M</creatorcontrib><creatorcontrib>Korenstein, Deborah</creatorcontrib><creatorcontrib>Ruchnewitz, Denis</creatorcontrib><creatorcontrib>Lässig, Michael</creatorcontrib><creatorcontrib>Łuksza, Marta</creatorcontrib><creatorcontrib>Greenbaum, Benjamin</creatorcontrib><creatorcontrib>Seshan, Venkatraman E</creatorcontrib><creatorcontrib>Esther Babady, N</creatorcontrib><creatorcontrib>Kamboj, Mini</creatorcontrib><title>Clinical and Genomic Characterization of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS CoV-2) Infections in mRNA Vaccinated Health Care Personnel in New York City</title><title>Clinical infectious diseases</title><addtitle>Clin Infect Dis</addtitle><description>Abstract
Background
Vaccine-induced clinical protection against severe acute respiratory syndrome coronavirus 2 (SARS CoV-2) variants is an evolving target. There are limited genomic level data on SARS CoV-2 breakthrough infections and vaccine effectiveness (VE) since the global spread of the B.1.617.2 (Delta) variant.
Methods
In a retrospective study from 1 November 2020 to 31 August 2021, divided as pre-Delta and Delta-dominant periods, laboratory-confirmed SARS CoV-2 infections among healthcare personnel (HCP) at a large tertiary cancer center in New York City were examined to compare the weekly infection rate-ratio in vaccinated, partially vaccinated, and unvaccinated HCP. We describe the clinical and genomic epidemiologic features of post-vaccine infections to assess for selection of variants of concern (VOC)/variants of interest (VOI) in the early post-vaccine period and impact of B.1.617.2 (Delta) variant domination on VE.
Results
Among 13658 HCP in our cohort, 12379 received at least 1 dose of a messenger RNA (mRNA) vaccine. In the pre-Delta period overall VE was 94.5%. Whole genome sequencing (WGS) of 369 isolates in the pre-Delta period did not reveal a clade bias for VOC/VOI specific to post-vaccine infections. VE in the Delta dominant phase was 75.6%. No hospitalizations occurred among vaccinated HCP in the entire study period, compared to 17 hospitalizations and 1 death among unvaccinated HCP.
Conclusions
Findings show high VE among HCP in New York City in the pre-Delta phase, with moderate decline in VE post-Delta emergence. SARS CoV-2 clades were similarly distributed among vaccinated and unvaccinated infected HCP without apparent clustering during the pre-Delta period of diverse clade circulation. Strong vaccine protection against hospitalization was maintained through the entire study period.
study of >13000 healthcare personnel (HCP) showed that messenger RNA (mRNA) vaccine effectiveness (VE) against coronavirus disease 2019 (COVID-19) was 94% through initial 5 months of follow-up, with moderate VE reduction to 75% during subsequent Delta-dominant period. No hospitalizations occurred among vaccinated HCP throughout the study period.</description><subject>COVID-19 - epidemiology</subject><subject>COVID-19 - prevention & control</subject><subject>Delivery of Health Care</subject><subject>Genomics</subject><subject>Humans</subject><subject>Major</subject><subject>New York City - epidemiology</subject><subject>Retrospective Studies</subject><subject>RNA, Messenger</subject><subject>SARS-CoV-2 - genetics</subject><issn>1058-4838</issn><issn>1537-6591</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kUGL1DAUx4so7rp68i45yYpUmyZp04swFN1dWFaZ0QVP4TV9daJtMibpyPiR_JRmmHHRi4eQ8PLj997jn2VPafGKFg17rU2fDnRSVveyUypYnVeioffTuxAy55LJk-xRCF-LglJZiIfZCeMV56xhp9mvdjTWaBgJ2J5coHWT0aRdgwcd0ZufEI2zxA1khVv0SBZ6jkiWGDbGQ3R-R1Y723s3IWmddxa2xs-BlOR8tViuUu02L1-QKzug3psCMZZMy5sFuQWtjYWIPblEGOOatJD8H9AHZy2Oe_AGf5DPzn8jrYm7x9mDAcaAT473Wfbp3duP7WV-_f7iql1c55rTMuZdVbGSpe3qAWDQusRG9LyDuhaIAimHBkTDSkpFU-tGDmVdSt1L1gHnopLsLHtz8G7mbsJeo40eRrXxZgK_Uw6M-vfHmrX64raqqWhZNzwJzo8C777PGKKaTNA4jmDRzUGVQqbujNM6oS8PqPYuBI_DXRtaqH26KqWrjukm-tnfk92xf-JMwPMD4ObNf02_Aa76sEg</recordid><startdate>20220824</startdate><enddate>20220824</enddate><creator>Robilotti, Elizabeth V</creator><creator>Whiting, Karissa</creator><creator>Lucca, Anabella</creator><creator>Poon, Chester</creator><creator>Guest, Rebecca</creator><creator>McMillen, Tracy</creator><creator>Jani, Krupa</creator><creator>Solovyov, Alexander</creator><creator>Kelson, Suzanne</creator><creator>Browne, Kevin</creator><creator>Freeswick, Scott</creator><creator>Hohl, Tobias M</creator><creator>Korenstein, Deborah</creator><creator>Ruchnewitz, Denis</creator><creator>Lässig, Michael</creator><creator>Łuksza, Marta</creator><creator>Greenbaum, Benjamin</creator><creator>Seshan, Venkatraman E</creator><creator>Esther Babady, N</creator><creator>Kamboj, Mini</creator><general>Oxford University Press</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20220824</creationdate><title>Clinical and Genomic Characterization of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS CoV-2) Infections in mRNA Vaccinated Health Care Personnel in New York City</title><author>Robilotti, Elizabeth V ; Whiting, Karissa ; Lucca, Anabella ; Poon, Chester ; Guest, Rebecca ; McMillen, Tracy ; Jani, Krupa ; Solovyov, Alexander ; Kelson, Suzanne ; Browne, Kevin ; Freeswick, Scott ; Hohl, Tobias M ; Korenstein, Deborah ; Ruchnewitz, Denis ; Lässig, Michael ; Łuksza, Marta ; Greenbaum, Benjamin ; Seshan, Venkatraman E ; Esther Babady, N ; Kamboj, Mini</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c412t-b663234397faafcc2e95d4ba775ee5e14a9a593211597c98f2728cd83ba445683</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>COVID-19 - epidemiology</topic><topic>COVID-19 - prevention & control</topic><topic>Delivery of Health Care</topic><topic>Genomics</topic><topic>Humans</topic><topic>Major</topic><topic>New York City - epidemiology</topic><topic>Retrospective Studies</topic><topic>RNA, Messenger</topic><topic>SARS-CoV-2 - genetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Robilotti, Elizabeth V</creatorcontrib><creatorcontrib>Whiting, Karissa</creatorcontrib><creatorcontrib>Lucca, Anabella</creatorcontrib><creatorcontrib>Poon, Chester</creatorcontrib><creatorcontrib>Guest, Rebecca</creatorcontrib><creatorcontrib>McMillen, Tracy</creatorcontrib><creatorcontrib>Jani, Krupa</creatorcontrib><creatorcontrib>Solovyov, Alexander</creatorcontrib><creatorcontrib>Kelson, Suzanne</creatorcontrib><creatorcontrib>Browne, Kevin</creatorcontrib><creatorcontrib>Freeswick, Scott</creatorcontrib><creatorcontrib>Hohl, Tobias M</creatorcontrib><creatorcontrib>Korenstein, Deborah</creatorcontrib><creatorcontrib>Ruchnewitz, Denis</creatorcontrib><creatorcontrib>Lässig, Michael</creatorcontrib><creatorcontrib>Łuksza, Marta</creatorcontrib><creatorcontrib>Greenbaum, Benjamin</creatorcontrib><creatorcontrib>Seshan, Venkatraman E</creatorcontrib><creatorcontrib>Esther Babady, N</creatorcontrib><creatorcontrib>Kamboj, Mini</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Clinical infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Robilotti, Elizabeth V</au><au>Whiting, Karissa</au><au>Lucca, Anabella</au><au>Poon, Chester</au><au>Guest, Rebecca</au><au>McMillen, Tracy</au><au>Jani, Krupa</au><au>Solovyov, Alexander</au><au>Kelson, Suzanne</au><au>Browne, Kevin</au><au>Freeswick, Scott</au><au>Hohl, Tobias M</au><au>Korenstein, Deborah</au><au>Ruchnewitz, Denis</au><au>Lässig, Michael</au><au>Łuksza, Marta</au><au>Greenbaum, Benjamin</au><au>Seshan, Venkatraman E</au><au>Esther Babady, N</au><au>Kamboj, Mini</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical and Genomic Characterization of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS CoV-2) Infections in mRNA Vaccinated Health Care Personnel in New York City</atitle><jtitle>Clinical infectious diseases</jtitle><addtitle>Clin Infect Dis</addtitle><date>2022-08-24</date><risdate>2022</risdate><volume>75</volume><issue>1</issue><spage>e774</spage><epage>e782</epage><pages>e774-e782</pages><issn>1058-4838</issn><eissn>1537-6591</eissn><abstract>Abstract
Background
Vaccine-induced clinical protection against severe acute respiratory syndrome coronavirus 2 (SARS CoV-2) variants is an evolving target. There are limited genomic level data on SARS CoV-2 breakthrough infections and vaccine effectiveness (VE) since the global spread of the B.1.617.2 (Delta) variant.
Methods
In a retrospective study from 1 November 2020 to 31 August 2021, divided as pre-Delta and Delta-dominant periods, laboratory-confirmed SARS CoV-2 infections among healthcare personnel (HCP) at a large tertiary cancer center in New York City were examined to compare the weekly infection rate-ratio in vaccinated, partially vaccinated, and unvaccinated HCP. We describe the clinical and genomic epidemiologic features of post-vaccine infections to assess for selection of variants of concern (VOC)/variants of interest (VOI) in the early post-vaccine period and impact of B.1.617.2 (Delta) variant domination on VE.
Results
Among 13658 HCP in our cohort, 12379 received at least 1 dose of a messenger RNA (mRNA) vaccine. In the pre-Delta period overall VE was 94.5%. Whole genome sequencing (WGS) of 369 isolates in the pre-Delta period did not reveal a clade bias for VOC/VOI specific to post-vaccine infections. VE in the Delta dominant phase was 75.6%. No hospitalizations occurred among vaccinated HCP in the entire study period, compared to 17 hospitalizations and 1 death among unvaccinated HCP.
Conclusions
Findings show high VE among HCP in New York City in the pre-Delta phase, with moderate decline in VE post-Delta emergence. SARS CoV-2 clades were similarly distributed among vaccinated and unvaccinated infected HCP without apparent clustering during the pre-Delta period of diverse clade circulation. Strong vaccine protection against hospitalization was maintained through the entire study period.
study of >13000 healthcare personnel (HCP) showed that messenger RNA (mRNA) vaccine effectiveness (VE) against coronavirus disease 2019 (COVID-19) was 94% through initial 5 months of follow-up, with moderate VE reduction to 75% during subsequent Delta-dominant period. No hospitalizations occurred among vaccinated HCP throughout the study period.</abstract><cop>US</cop><pub>Oxford University Press</pub><pmid>34644393</pmid><doi>10.1093/cid/ciab886</doi><oa>free_for_read</oa></addata></record> |
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subjects | COVID-19 - epidemiology COVID-19 - prevention & control Delivery of Health Care Genomics Humans Major New York City - epidemiology Retrospective Studies RNA, Messenger SARS-CoV-2 - genetics |
title | Clinical and Genomic Characterization of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS CoV-2) Infections in mRNA Vaccinated Health Care Personnel in New York City |
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