Robust humoral and cellular immune responses and low risk for reinfection at least 8 months following asymptomatic to mild COVID-19.


Journal

Journal of internal medicine
ISSN: 1365-2796
Titre abrégé: J Intern Med
Pays: England
ID NLM: 8904841

Informations de publication

Date de publication:
01 2022
Historique:
pubmed: 31 8 2021
medline: 11 1 2022
entrez: 30 8 2021
Statut: ppublish

Résumé

Emerging data support detectable immune responses for months after severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and vaccination, but it is not yet established to what degree and for how long protection against reinfection lasts. We investigated SARS-CoV-2-specific humoral and cellular immune responses more than 8 months post-asymptomatic, mild and severe infection in a cohort of 1884 healthcare workers (HCW) and 51 hospitalized COVID-19 patients. Possible protection against SARS-CoV-2 reinfection was analyzed by a weekly 3-month polymerase chain reaction (PCR) screening of 252 HCW that had seroconverted 7 months prior to start of screening and 48 HCW that had remained seronegative at multiple time points. All COVID-19 patients and 96% (355/370) of HCW who were anti-spike IgG positive at inclusion remained anti-spike IgG positive at the 8-month follow-up. Circulating SARS-CoV-2-specific memory T cell responses were detected in 88% (45/51) of COVID-19 patients and in 63% (233/370) of seropositive HCW. The cumulative incidence of PCR-confirmed SARS-CoV-2 infection was 1% (3/252) among anti-spike IgG positive HCW (0.13 cases per 100 weeks at risk) compared to 23% (11/48) among anti-spike IgG negative HCW (2.78 cases per 100 weeks at risk), resulting in a protective effect of 95.2% (95% CI 81.9%-99.1%). The vast majority of anti-spike IgG positive individuals remain anti-spike IgG positive for at least 8 months regardless of initial COVID-19 disease severity. The presence of anti-spike IgG antibodies is associated with a substantially reduced risk of reinfection up to 9 months following asymptomatic to mild COVID-19.

Sections du résumé

BACKGROUND
Emerging data support detectable immune responses for months after severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and vaccination, but it is not yet established to what degree and for how long protection against reinfection lasts.
METHODS
We investigated SARS-CoV-2-specific humoral and cellular immune responses more than 8 months post-asymptomatic, mild and severe infection in a cohort of 1884 healthcare workers (HCW) and 51 hospitalized COVID-19 patients. Possible protection against SARS-CoV-2 reinfection was analyzed by a weekly 3-month polymerase chain reaction (PCR) screening of 252 HCW that had seroconverted 7 months prior to start of screening and 48 HCW that had remained seronegative at multiple time points.
RESULTS
All COVID-19 patients and 96% (355/370) of HCW who were anti-spike IgG positive at inclusion remained anti-spike IgG positive at the 8-month follow-up. Circulating SARS-CoV-2-specific memory T cell responses were detected in 88% (45/51) of COVID-19 patients and in 63% (233/370) of seropositive HCW. The cumulative incidence of PCR-confirmed SARS-CoV-2 infection was 1% (3/252) among anti-spike IgG positive HCW (0.13 cases per 100 weeks at risk) compared to 23% (11/48) among anti-spike IgG negative HCW (2.78 cases per 100 weeks at risk), resulting in a protective effect of 95.2% (95% CI 81.9%-99.1%).
CONCLUSIONS
The vast majority of anti-spike IgG positive individuals remain anti-spike IgG positive for at least 8 months regardless of initial COVID-19 disease severity. The presence of anti-spike IgG antibodies is associated with a substantially reduced risk of reinfection up to 9 months following asymptomatic to mild COVID-19.

Identifiants

pubmed: 34459525
doi: 10.1111/joim.13387
pmc: PMC8661920
doi:

Substances chimiques

Antibodies, Viral 0
Immunoglobulin G 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

72-80

Informations de copyright

© 2021 The Authors. Journal of Internal Medicine published by John Wiley & Sons Ltd on behalf of Association for Publication of The Journal of Internal Medicine.

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Auteurs

Sebastian Havervall (S)

Department of Clinical Sciences, Karolinska Institutet Danderyd Hospital, Stockholm, Sweden.

Henry Ng (H)

Department of Clinical Sciences, Karolinska Institutet Danderyd Hospital, Stockholm, Sweden.
Department of Medical Cell Biology, Uppsala University, Uppsala, Sweden.

August Jernbom Falk (A)

Department of Protein Science, SciLifeLab, KTH Royal Institute of Technology, Stockholm, Sweden.

Nina Greilert-Norin (N)

Department of Clinical Sciences, Karolinska Institutet Danderyd Hospital, Stockholm, Sweden.

Anna Månberg (A)

Department of Protein Science, SciLifeLab, KTH Royal Institute of Technology, Stockholm, Sweden.

Ulrika Marking (U)

Department of Clinical Sciences, Karolinska Institutet Danderyd Hospital, Stockholm, Sweden.

Ida Laurén (I)

Department of Pharmacy, Uppsala University, Uppsala, Sweden.

Lena Gabrielsson (L)

Department of Clinical Sciences, Karolinska Institutet Danderyd Hospital, Stockholm, Sweden.

Ann-Christin Salomonsson (AC)

Department of Clinical Sciences, Karolinska Institutet Danderyd Hospital, Stockholm, Sweden.

Katherina Aguilera (K)

Department of Clinical Sciences, Karolinska Institutet Danderyd Hospital, Stockholm, Sweden.

Martha Kihlgren (M)

Department of Clinical Sciences, Karolinska Institutet Danderyd Hospital, Stockholm, Sweden.

Maja Månsson (M)

Department of Clinical Sciences, Karolinska Institutet Danderyd Hospital, Stockholm, Sweden.

Axel Rosell (A)

Department of Clinical Sciences, Karolinska Institutet Danderyd Hospital, Stockholm, Sweden.

Cecilia Hellström (C)

Department of Protein Science, SciLifeLab, KTH Royal Institute of Technology, Stockholm, Sweden.

Eni Andersson (E)

Department of Protein Science, SciLifeLab, KTH Royal Institute of Technology, Stockholm, Sweden.

Jennie Olofsson (J)

Department of Protein Science, SciLifeLab, KTH Royal Institute of Technology, Stockholm, Sweden.

Lovisa Skoglund (L)

Department of Protein Science, SciLifeLab, KTH Royal Institute of Technology, Stockholm, Sweden.

Jamil Yousef (J)

Department of Protein Science, SciLifeLab, KTH Royal Institute of Technology, Stockholm, Sweden.

Elisa Pin (E)

Department of Protein Science, SciLifeLab, KTH Royal Institute of Technology, Stockholm, Sweden.

Martin Lord (M)

Department of Pharmacy, Uppsala University, Uppsala, Sweden.

Mikael Åberg (M)

Department of Medical Sciences, Clinical Chemistry and Science for Life Laboratory, Uppsala University, Uppsala, Sweden.

My Hedhammar (M)

Department of Protein Science, SciLifeLab, KTH Royal Institute of Technology, Stockholm, Sweden.

Hanna Tegel (H)

Department of Protein Science, SciLifeLab, KTH Royal Institute of Technology, Stockholm, Sweden.

Pierre Dönnes (P)

SciCross AB, Skövde, Sweden.

Mia Phillipson (M)

Department of Medical Cell Biology, Uppsala University, Uppsala, Sweden.

Peter Nilsson (P)

Department of Protein Science, SciLifeLab, KTH Royal Institute of Technology, Stockholm, Sweden.

Jonas Klingström (J)

Centre for Infectious Medicine, Department of Medicine Huddinge, Karolinska Institutet, Stockholm, Sweden.

Sara Mangsbo (S)

Department of Pharmacy, Uppsala University, Uppsala, Sweden.

Sophia Hober (S)

Department of Protein Science, SciLifeLab, KTH Royal Institute of Technology, Stockholm, Sweden.

Charlotte Thålin (C)

Department of Clinical Sciences, Karolinska Institutet Danderyd Hospital, Stockholm, Sweden.

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