Evidence map›Paper›PMID 33844963›Full record

ArticleLancet (London, England)2021

SARS-CoV-2 infection rates of antibody-positive compared with antibody-negative health-care workers in England: a large, multicentre, prospective cohort study (SIREN).

Victoria Jane Hall, Sarah Foulkes, Andre Charlett, Ana Atti, Edward J M Monk, Ruth Simmons, Edgar Wellington, Michelle J Cole, Ayoub Saei, Blanche Oguti and 14 more

Erratum issued Registry-linked trialOpen access · bronzeAbstract readMulticenter Study
In one paragraph

Article in Lancet (London, England), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT05774093 (Evaluation of COVID-19 Immune Barrier and Reinfection Risk), which is not on this map. Cited by 393 papers, 9 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
393citing papers in PubMed, 9 pooled it
45.3field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT05774093 recruitingnot on this mapstarted 2023, after this paper: background citation

Evaluation of COVID-19 Immune Barrier and Reinfection Risk

TypeobservationalSponsorSun Yat-sen UniversityRan2023 to 2027Enrolled300ConditionsCOVID-19 Infection, Immunization, Infection
3 · Its place in the literature

Who cites it

393 citing papers in PubMed, 9 syntheses or guidelines pooled it, 735 citations in OpenAlex.

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  15. Effectiveness of COVID-19 Vaccination and Prior Infections to Reduce Long COVID Risk During the Pre-Omicron and Omicron Periods.Clinical infectious diseases : an official publication of the Infectious Diseases Society of America · 2026
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333 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors at 4 institutions in 1 country.

Victoria Jane HallPublic Health England Colindale, Colindale, London, UK; The National Institute for Health Research Health Protection Research Unit in Healthcare Associated Infections and Antimicrobial Resistance at the University of Oxford, University of Oxford, Oxford, UK.
Sarah FoulkesPublic Health England Colindale, Colindale, London, UK.
Andre CharlettPublic Health England Colindale, Colindale, London, UK; The National Institute for Health Research Health Protection Research Unit in Behavioural Science and Evaluation at University of Bristol in partnership with Public Health England, Bristol, UK.
Ana AttiPublic Health England Colindale, Colindale, London, UK.
Edward J M MonkPublic Health England Colindale, Colindale, London, UK.
Ruth SimmonsPublic Health England Colindale, Colindale, London, UK.
Edgar WellingtonPublic Health England Colindale, Colindale, London, UK.
Michelle J ColePublic Health England Colindale, Colindale, London, UK.
Ayoub SaeiPublic Health England Colindale, Colindale, London, UK.
Blanche OgutiPublic Health England Colindale, Colindale, London, UK; Oxford Vaccine Group, University of Oxford, Oxford, UK.
Katie MunroPublic Health England Colindale, Colindale, London, UK.
Sarah WallacePublic Health England Colindale, Colindale, London, UK.
Peter D KirwanPublic Health England Colindale, Colindale, London, UK; Medical Research Council Biostatistics Unit, University of Cambridge, Cambridge, UK.
Madhumita ShrotriPublic Health England Colindale, Colindale, London, UK.
Amoolya VusirikalaPublic Health England Colindale, Colindale, London, UK.
Sakib RokadiyaPublic Health England Colindale, Colindale, London, UK.
Meaghan KallPublic Health England Colindale, Colindale, London, UK.
Maria ZambonPublic Health England Colindale, Colindale, London, UK.
Mary RamsayPublic Health England Colindale, Colindale, London, UK; Oxford Vaccine Group, University of Oxford, Oxford, UK.
Tim BrooksPublic Health England Colindale, Colindale, London, UK.
Colin S BrownPublic Health England Colindale, Colindale, London, UK.
Meera A ChandPublic Health England Colindale, Colindale, London, UK; Guys and St Thomas's Hospital NHS Trust, London, UK.
Susan HopkinsPublic Health England Colindale, Colindale, London, UK; The National Institute for Health Research Health Protection Research Unit in Healthcare Associated Infections and Antimicrobial Resistance at the University of Oxford, University of Oxford, Oxford, UK. Electronic address: susan.hopkins@phe.gov.uk.
SIREN Study Group
Public Health England · GBScottish Government · GBSt Thomas' Hospital · GBUniversity of Cambridge · GB

Funding

Medical Research Council MC_PC_20060Medical Research Council MC_UU_00002/11Wellcome Trust 109965/Z/15/ZWellcome Trust 211153/Z/18/Z
6 · The paper itself

Abstract

backgroundIncreased understanding of whether individuals who have recovered from COVID-19 are protected from future SARS-CoV-2 infection is an urgent requirement. We aimed to investigate whether antibodies against SARS-CoV-2 were associated with a decreased risk of symptomatic and asymptomatic reinfection.

methodsA large, multicentre, prospective cohort study was done, with participants recruited from publicly funded hospitals in all regions of England. All health-care workers, support staff, and administrative staff working at hospitals who could remain engaged in follow-up for 12 months were eligible to join The SARS-CoV-2 Immunity and Reinfection Evaluation study. Participants were excluded if they had no PCR tests after enrolment, enrolled after Dec 31, 2020, or had insufficient PCR and antibody data for cohort assignment. Participants attended regular SARS-CoV-2 PCR and antibody testing (every 2-4 weeks) and completed questionnaires every 2 weeks on symptoms and exposures. At enrolment, participants were assigned to either the positive cohort (antibody positive, or previous positive PCR or antibody test) or negative cohort (antibody negative, no previous positive PCR or antibody test). The primary outcome was a reinfection in the positive cohort or a primary infection in the negative cohort, determined by PCR tests. Potential reinfections were clinically reviewed and classified according to case definitions (confirmed, probable, or possible) and symptom-status, depending on the hierarchy of evidence. Primary infections in the negative cohort were defined as a first positive PCR test and seroconversions were excluded when not associated with a positive PCR test. A proportional hazards frailty model using a Poisson distribution was used to estimate incidence rate ratios (IRR) to compare infection rates in the two cohorts.

findingsFrom June 18, 2020, to Dec 31, 2020, 30 625 participants were enrolled into the study. 51 participants withdrew from the study, 4913 were excluded, and 25 661 participants (with linked data on antibody and PCR testing) were included in the analysis. Data were extracted from all sources on Feb 5, 2021, and include data up to and including Jan 11, 2021. 155 infections were detected in the baseline positive cohort of 8278 participants, collectively contributing 2 047 113 person-days of follow-up. This compares with 1704 new PCR positive infections in the negative cohort of 17 383 participants, contributing 2 971 436 person-days of follow-up. The incidence density was 7·6 reinfections per 100 000 person-days in the positive cohort, compared with 57·3 primary infections per 100 000 person-days in the negative cohort, between June, 2020, and January, 2021. The adjusted IRR was 0·159 for all reinfections (95% CI 0·13-0·19) compared with PCR-confirmed primary infections. The median interval between primary infection and reinfection was more than 200 days.

interpretationA previous history of SARS-CoV-2 infection was associated with an 84% lower risk of infection, with median protective effect observed 7 months following primary infection. This time period is the minimum probable effect because seroconversions were not included. This study shows that previous infection with SARS-CoV-2 induces effective immunity to future infections in most individuals.

fundingDepartment of Health and Social Care of the UK Government, Public Health England, The National Institute for Health Research, with contributions from the Scottish, Welsh and Northern Irish governments.

Indexed as

Health PersonnelAdultAntibodies, ViralAsymptomatic InfectionsCOVID-19COVID-19 Nucleic Acid TestingEnglandFemaleFollow-Up StudiesHumansMaleMiddle AgedPandemicsProspective StudiesReinfectionRisk FactorsAntibodies, Viral

Identifiers

PMID33844963
PMCPMC8040523
OpenAlexW3153039449

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.