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

被引:51
作者
Lumley, Sheila F. [1 ,2 ,3 ,4 ]
Rodger, Gillian [2 ]
Constantinides, Bede [2 ]
Sanderson, Nicholas [2 ,3 ]
Chau, Kevin K. [2 ]
Street, Teresa L. [2 ,3 ]
O'Donnell, Denise [2 ]
Howarth, Alison [2 ]
Hatch, Stephanie B. [2 ]
Marsden, Brian D. [2 ,5 ]
Cox, Stuart [1 ]
James, Tim [1 ]
Warren, Fiona [1 ]
Peck, Liam J. [6 ]
Ritter, Thomas G. [6 ]
de Toledo, Zoe [6 ]
Warren, Laura [1 ]
Axten, David [1 ]
Cornall, Richard J. [2 ]
Jones, E. Yvonne [2 ]
Stuart, David, I [2 ]
Screaton, Gavin [2 ]
Ebner, Daniel [2 ,7 ]
Hoosdally, Sarah [2 ,3 ,4 ]
Chand, Meera [8 ]
Crook, Derrick W. [2 ,3 ,4 ]
O'donnell, Anne-Marie [1 ,9 ]
Conlon, Christopher P. [2 ]
Pouwels, Koen B. [4 ,9 ]
Walker, A. Sarah [2 ,3 ,4 ]
Peto, Tim E. A. [2 ,3 ,4 ]
Hopkins, Susan [8 ]
Walker, Timothy M. [2 ,10 ]
Stoesser, Nicole E. [1 ,2 ,3 ,4 ]
Matthews, Philippa C. [1 ,2 ,3 ,4 ]
Jeffery, Katie [1 ]
Eyre, David W. [3 ,4 ,9 ,11 ]
机构
[1] Oxford Univ Hosp NHS Fdn Trust, Oxford, England
[2] Univ Oxford, Nuffield Dept Med, Oxford, England
[3] Univ Oxford, NIHR Oxford Biomed Res Ctr, Oxford, England
[4] Univ Oxford, NIHR Hlth Protect Res Unit Healthcare Associated, Publ Hlth England, Oxford, England
[5] Univ Oxford, Kennedy Inst Rheumatol Res, Oxford, England
[6] Univ Oxford, Med Sch, Oxford, England
[7] Univ Oxford, Target Discovery Inst, Oxford, England
[8] Publ Hlth England Colindale, Natl Infect Serv, London, England
[9] Univ Oxford, Nuffield Dept Populat Hlth, Oxford, England
[10] Univ Oxford, Clin Res Unit, Ho Chi Minh City, Vietnam
[11] Univ Oxford, Big Data Inst, Oxford, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
SARS-CoV-2; vaccine; antibody; healthcare worker; immunity; COVID-19;
D O I
10.1093/cid/ciab608
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
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. Natural infection resulting in detectable anti-spike antibodies and two vaccine doses both provided >= 85% protection against symptomatic and asymptomatic SARS-CoV-2 infection in healthcare workers, including against the B.1.1.7 variant. Single dose vaccination reduced symptomatic infection by 67%.
引用
收藏
页码:1208 / 1219
页数:12
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