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An Observational Cohort Study on the Incidence of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection and B.1.1.7 Variant Infection in Healthcare Workers by Antibody and Vaccination Status

BACKGROUND: Natural and vaccine-induced immunity will play a key role in controlling the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic. SARS-CoV-2 variants have the potential to evade natural and vaccine-induced immunity. METHODS: In a longitudinal cohort study of healthcare...

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Autores principales: Lumley, Sheila F, Rodger, Gillian, Constantinides, Bede, Sanderson, Nicholas, Chau, Kevin K, Street, Teresa L, O’Donnell, Denise, Howarth, Alison, Hatch, Stephanie B, Marsden, Brian D, Cox, Stuart, James, Tim, Warren, Fiona, Peck, Liam J, Ritter, Thomas G, de Toledo, Zoe, Warren, Laura, Axten, David, Cornall, Richard J, Jones, E Yvonne, Stuart, David I, Screaton, Gavin, Ebner, Daniel, Hoosdally, Sarah, Chand, Meera, Crook, Derrick W, O’Donnell, Anne-Marie, Conlon, Christopher P, Pouwels, Koen B, Walker, A Sarah, Peto, Tim E A, Hopkins, Susan, Walker, Timothy M, Stoesser, Nicole E, Matthews, Philippa C, Jeffery, Katie, Eyre, David W
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8994591/
https://www.ncbi.nlm.nih.gov/pubmed/34216472
http://dx.doi.org/10.1093/cid/ciab608
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author Lumley, Sheila F
Rodger, Gillian
Constantinides, Bede
Sanderson, Nicholas
Chau, Kevin K
Street, Teresa L
O’Donnell, Denise
Howarth, Alison
Hatch, Stephanie B
Marsden, Brian D
Cox, Stuart
James, Tim
Warren, Fiona
Peck, Liam J
Ritter, Thomas G
de Toledo, Zoe
Warren, Laura
Axten, David
Cornall, Richard J
Jones, E Yvonne
Stuart, David I
Screaton, Gavin
Ebner, Daniel
Hoosdally, Sarah
Chand, Meera
Crook, Derrick W
O’Donnell, Anne-Marie
Conlon, Christopher P
Pouwels, Koen B
Walker, A Sarah
Peto, Tim E A
Hopkins, Susan
Walker, Timothy M
Stoesser, Nicole E
Matthews, Philippa C
Jeffery, Katie
Eyre, David W
author_facet Lumley, Sheila F
Rodger, Gillian
Constantinides, Bede
Sanderson, Nicholas
Chau, Kevin K
Street, Teresa L
O’Donnell, Denise
Howarth, Alison
Hatch, Stephanie B
Marsden, Brian D
Cox, Stuart
James, Tim
Warren, Fiona
Peck, Liam J
Ritter, Thomas G
de Toledo, Zoe
Warren, Laura
Axten, David
Cornall, Richard J
Jones, E Yvonne
Stuart, David I
Screaton, Gavin
Ebner, Daniel
Hoosdally, Sarah
Chand, Meera
Crook, Derrick W
O’Donnell, Anne-Marie
Conlon, Christopher P
Pouwels, Koen B
Walker, A Sarah
Peto, Tim E A
Hopkins, Susan
Walker, Timothy M
Stoesser, Nicole E
Matthews, Philippa C
Jeffery, Katie
Eyre, David W
author_sort Lumley, Sheila F
collection PubMed
description BACKGROUND: Natural and vaccine-induced immunity will play a key role in controlling the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic. SARS-CoV-2 variants have the potential to evade natural and vaccine-induced immunity. METHODS: In a longitudinal cohort study of healthcare workers (HCWs) in Oxfordshire, United Kingdom, we investigated the protection from symptomatic and asymptomatic polymerase chain reaction (PCR)-confirmed SARS-CoV-2 infection conferred by vaccination (Pfizer-BioNTech BNT162b2, Oxford-AstraZeneca ChAdOx1 nCOV-19) and prior infection (determined using anti-spike antibody status), using Poisson regression adjusted for age, sex, temporal changes in incidence and role. We estimated protection conferred after 1 versus 2 vaccinations and from infections with the B.1.1.7 variant identified using whole genome sequencing. RESULTS: In total, 13 109 HCWs participated; 8285 received the Pfizer-BioNTech vaccine (1407 two doses), and 2738 the Oxford-AstraZeneca vaccine (49 two doses). Compared to unvaccinated seronegative HCWs, natural immunity and 2 vaccination doses provided similar protection against symptomatic infection: no HCW vaccinated twice had symptomatic infection, and incidence was 98% lower in seropositive HCWs (adjusted incidence rate ratio 0.02 [95% confidence interval {CI} < .01–.18]). Two vaccine doses or seropositivity reduced the incidence of any PCR-positive result with or without symptoms by 90% (0.10 [95% CI .02–.38]) and 85% (0.15 [95% CI .08–.26]), respectively. Single-dose vaccination reduced the incidence of symptomatic infection by 67% (0.33 [95% CI .21–.52]) and any PCR-positive result by 64% (0.36 [95% CI .26–.50]). There was no evidence of differences in immunity induced by natural infection and vaccination for infections with S-gene target failure and B.1.1.7. CONCLUSIONS: Natural infection resulting in detectable anti-spike antibodies and 2 vaccine doses both provide robust protection against SARS-CoV-2 infection, including against the B.1.1.7 variant.
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spelling pubmed-89945912022-04-11 An Observational Cohort Study on the Incidence of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection and B.1.1.7 Variant Infection in Healthcare Workers by Antibody and Vaccination Status Lumley, Sheila F Rodger, Gillian Constantinides, Bede Sanderson, Nicholas Chau, Kevin K Street, Teresa L O’Donnell, Denise Howarth, Alison Hatch, Stephanie B Marsden, Brian D Cox, Stuart James, Tim Warren, Fiona Peck, Liam J Ritter, Thomas G de Toledo, Zoe Warren, Laura Axten, David Cornall, Richard J Jones, E Yvonne Stuart, David I Screaton, Gavin Ebner, Daniel Hoosdally, Sarah Chand, Meera Crook, Derrick W O’Donnell, Anne-Marie Conlon, Christopher P Pouwels, Koen B Walker, A Sarah Peto, Tim E A Hopkins, Susan Walker, Timothy M Stoesser, Nicole E Matthews, Philippa C Jeffery, Katie Eyre, David W Clin Infect Dis Major Articles and Commentaries BACKGROUND: Natural and vaccine-induced immunity will play a key role in controlling the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic. SARS-CoV-2 variants have the potential to evade natural and vaccine-induced immunity. METHODS: In a longitudinal cohort study of healthcare workers (HCWs) in Oxfordshire, United Kingdom, we investigated the protection from symptomatic and asymptomatic polymerase chain reaction (PCR)-confirmed SARS-CoV-2 infection conferred by vaccination (Pfizer-BioNTech BNT162b2, Oxford-AstraZeneca ChAdOx1 nCOV-19) and prior infection (determined using anti-spike antibody status), using Poisson regression adjusted for age, sex, temporal changes in incidence and role. We estimated protection conferred after 1 versus 2 vaccinations and from infections with the B.1.1.7 variant identified using whole genome sequencing. RESULTS: In total, 13 109 HCWs participated; 8285 received the Pfizer-BioNTech vaccine (1407 two doses), and 2738 the Oxford-AstraZeneca vaccine (49 two doses). Compared to unvaccinated seronegative HCWs, natural immunity and 2 vaccination doses provided similar protection against symptomatic infection: no HCW vaccinated twice had symptomatic infection, and incidence was 98% lower in seropositive HCWs (adjusted incidence rate ratio 0.02 [95% confidence interval {CI} < .01–.18]). Two vaccine doses or seropositivity reduced the incidence of any PCR-positive result with or without symptoms by 90% (0.10 [95% CI .02–.38]) and 85% (0.15 [95% CI .08–.26]), respectively. Single-dose vaccination reduced the incidence of symptomatic infection by 67% (0.33 [95% CI .21–.52]) and any PCR-positive result by 64% (0.36 [95% CI .26–.50]). There was no evidence of differences in immunity induced by natural infection and vaccination for infections with S-gene target failure and B.1.1.7. CONCLUSIONS: Natural infection resulting in detectable anti-spike antibodies and 2 vaccine doses both provide robust protection against SARS-CoV-2 infection, including against the B.1.1.7 variant. Oxford University Press 2021-07-03 /pmc/articles/PMC8994591/ /pubmed/34216472 http://dx.doi.org/10.1093/cid/ciab608 Text en © The Author(s) 2021. Published by Oxford University Press for the Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Major Articles and Commentaries
Lumley, Sheila F
Rodger, Gillian
Constantinides, Bede
Sanderson, Nicholas
Chau, Kevin K
Street, Teresa L
O’Donnell, Denise
Howarth, Alison
Hatch, Stephanie B
Marsden, Brian D
Cox, Stuart
James, Tim
Warren, Fiona
Peck, Liam J
Ritter, Thomas G
de Toledo, Zoe
Warren, Laura
Axten, David
Cornall, Richard J
Jones, E Yvonne
Stuart, David I
Screaton, Gavin
Ebner, Daniel
Hoosdally, Sarah
Chand, Meera
Crook, Derrick W
O’Donnell, Anne-Marie
Conlon, Christopher P
Pouwels, Koen B
Walker, A Sarah
Peto, Tim E A
Hopkins, Susan
Walker, Timothy M
Stoesser, Nicole E
Matthews, Philippa C
Jeffery, Katie
Eyre, David W
An Observational Cohort Study on the Incidence of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection and B.1.1.7 Variant Infection in Healthcare Workers by Antibody and Vaccination Status
title An Observational Cohort Study on the Incidence of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection and B.1.1.7 Variant Infection in Healthcare Workers by Antibody and Vaccination Status
title_full An Observational Cohort Study on the Incidence of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection and B.1.1.7 Variant Infection in Healthcare Workers by Antibody and Vaccination Status
title_fullStr An Observational Cohort Study on the Incidence of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection and B.1.1.7 Variant Infection in Healthcare Workers by Antibody and Vaccination Status
title_full_unstemmed An Observational Cohort Study on the Incidence of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection and B.1.1.7 Variant Infection in Healthcare Workers by Antibody and Vaccination Status
title_short An Observational Cohort Study on the Incidence of Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection and B.1.1.7 Variant Infection in Healthcare Workers by Antibody and Vaccination Status
title_sort observational cohort study on the incidence of severe acute respiratory syndrome coronavirus 2 (sars-cov-2) infection and b.1.1.7 variant infection in healthcare workers by antibody and vaccination status
topic Major Articles and Commentaries
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8994591/
https://www.ncbi.nlm.nih.gov/pubmed/34216472
http://dx.doi.org/10.1093/cid/ciab608
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