Dynamics of SARS-CoV-2 neutralising antibody responses and duration of immunity: a longitudinal study.


Journal

The Lancet. Microbe
ISSN: 2666-5247
Titre abrégé: Lancet Microbe
Pays: England
ID NLM: 101769019

Informations de publication

Date de publication:
06 2021
Historique:
pubmed: 30 3 2021
medline: 30 3 2021
entrez: 29 3 2021
Statut: ppublish

Résumé

Studies have found different waning rates of neutralising antibodies compared with binding antibodies against SARS-CoV-2. The impact of neutralising antibody waning rate at the individual patient level on the longevity of immunity remains unknown. We aimed to investigate the peak levels and dynamics of neutralising antibody waning and IgG avidity maturation over time, and correlate this with clinical parameters, cytokines, and T-cell responses. We did a longitudinal study of patients who had recovered from COVID-19 up to day 180 post-symptom onset by monitoring changes in neutralising antibody levels using a previously validated surrogate virus neutralisation test. Changes in antibody avidities and other immune markers at different convalescent stages were determined and correlated with clinical features. Using a machine learning algorithm, temporal change in neutralising antibody levels was classified into five groups and used to predict the longevity of neutralising antibody-mediated immunity. We approached 517 patients for participation in the study, of whom 288 consented for outpatient follow-up and collection of serial blood samples. 164 patients were followed up and had adequate blood samples collected for analysis, with a total of 546 serum samples collected, including 128 blood samples taken up to 180 days post-symptom onset. We identified five distinctive patterns of neutralising antibody dynamics as follows: negative, individuals who did not, at our intervals of sampling, develop neutralising antibodies at the 30% inhibition level (19 [12%] of 164 patients); rapid waning, individuals who had varying levels of neutralising antibodies from around 20 days after symptom onset, but seroreverted in less than 180 days (44 [27%] of 164 patients); slow waning, individuals who remained neutralising antibody-positive at 180 days post-symptom onset (46 [28%] of 164 patients); persistent, although with varying peak neutralising antibody levels, these individuals had minimal neutralising antibody decay (52 [32%] of 164 patients); and delayed response, a small group that showed an unexpected increase of neutralising antibodies during late convalescence (at 90 or 180 days after symptom onset; three [2%] of 164 patients). Persistence of neutralising antibodies was associated with disease severity and sustained level of pro-inflammatory cytokines, chemokines, and growth factors. By contrast, T-cell responses were similar among the different neutralising antibody dynamics groups. On the basis of the different decay dynamics, we established a prediction algorithm that revealed a wide range of neutralising antibody longevity, varying from around 40 days to many decades. Neutralising antibody response dynamics in patients who have recovered from COVID-19 vary greatly, and prediction of immune longevity can only be accurately determined at the individual level. Our findings emphasise the importance of public health and social measures in the ongoing pandemic outbreak response, and might have implications for longevity of immunity after vaccination. National Medical Research Council, Biomedical Research Council, and A*STAR, Singapore.

Sections du résumé

BACKGROUND
Studies have found different waning rates of neutralising antibodies compared with binding antibodies against SARS-CoV-2. The impact of neutralising antibody waning rate at the individual patient level on the longevity of immunity remains unknown. We aimed to investigate the peak levels and dynamics of neutralising antibody waning and IgG avidity maturation over time, and correlate this with clinical parameters, cytokines, and T-cell responses.
METHODS
We did a longitudinal study of patients who had recovered from COVID-19 up to day 180 post-symptom onset by monitoring changes in neutralising antibody levels using a previously validated surrogate virus neutralisation test. Changes in antibody avidities and other immune markers at different convalescent stages were determined and correlated with clinical features. Using a machine learning algorithm, temporal change in neutralising antibody levels was classified into five groups and used to predict the longevity of neutralising antibody-mediated immunity.
FINDINGS
We approached 517 patients for participation in the study, of whom 288 consented for outpatient follow-up and collection of serial blood samples. 164 patients were followed up and had adequate blood samples collected for analysis, with a total of 546 serum samples collected, including 128 blood samples taken up to 180 days post-symptom onset. We identified five distinctive patterns of neutralising antibody dynamics as follows: negative, individuals who did not, at our intervals of sampling, develop neutralising antibodies at the 30% inhibition level (19 [12%] of 164 patients); rapid waning, individuals who had varying levels of neutralising antibodies from around 20 days after symptom onset, but seroreverted in less than 180 days (44 [27%] of 164 patients); slow waning, individuals who remained neutralising antibody-positive at 180 days post-symptom onset (46 [28%] of 164 patients); persistent, although with varying peak neutralising antibody levels, these individuals had minimal neutralising antibody decay (52 [32%] of 164 patients); and delayed response, a small group that showed an unexpected increase of neutralising antibodies during late convalescence (at 90 or 180 days after symptom onset; three [2%] of 164 patients). Persistence of neutralising antibodies was associated with disease severity and sustained level of pro-inflammatory cytokines, chemokines, and growth factors. By contrast, T-cell responses were similar among the different neutralising antibody dynamics groups. On the basis of the different decay dynamics, we established a prediction algorithm that revealed a wide range of neutralising antibody longevity, varying from around 40 days to many decades.
INTERPRETATION
Neutralising antibody response dynamics in patients who have recovered from COVID-19 vary greatly, and prediction of immune longevity can only be accurately determined at the individual level. Our findings emphasise the importance of public health and social measures in the ongoing pandemic outbreak response, and might have implications for longevity of immunity after vaccination.
FUNDING
National Medical Research Council, Biomedical Research Council, and A*STAR, Singapore.

Identifiants

pubmed: 33778792
doi: 10.1016/S2666-5247(21)00025-2
pii: S2666-5247(21)00025-2
pmc: PMC7987301
doi:

Substances chimiques

Antibodies, Neutralizing 0
Antibodies, Viral 0
Cytokines 0

Types de publication

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

Langues

eng

Pagination

e240-e249

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© 2021 The Author(s). Published by Elsevier Ltd. This is an Open Access article under the CC BY-NC-ND 4.0 license.

Auteurs

Wan Ni Chia (WN)

Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore.

Feng Zhu (F)

Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore.

Sean Wei Xiang Ong (SWX)

National Centre for Infectious Diseases, Singapore.
Department of Infectious Diseases, Tan Tock Seng Hospital, Singapore.

Barnaby Edward Young (BE)

National Centre for Infectious Diseases, Singapore.
Department of Infectious Diseases, Tan Tock Seng Hospital, Singapore.
Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore.

Siew-Wai Fong (SW)

ASTAR Infectious Diseases Labs, Agency for Science, Technology and Research, Singapore.
Singapore Immunology Network, Agency for Science, Technology and Research, Singapore.

Nina Le Bert (N)

Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore.

Chee Wah Tan (CW)

Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore.

Charles Tiu (C)

Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore.

Jinyan Zhang (J)

Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore.

Seow Yen Tan (SY)

Department of Infectious Diseases, Changi General Hospital, Singapore.

Surinder Pada (S)

Division of Infectious Diseases, Ng Teng Fong General Hospital, Singapore.

Yi-Hao Chan (YH)

ASTAR Infectious Diseases Labs, Agency for Science, Technology and Research, Singapore.
Singapore Immunology Network, Agency for Science, Technology and Research, Singapore.

Christine Y L Tham (CYL)

Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore.

Kamini Kunasegaran (K)

Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore.

Mark I-C Chen (MI)

National Centre for Infectious Diseases, Singapore.
Department of Infectious Diseases, Tan Tock Seng Hospital, Singapore.

Jenny G H Low (JGH)

Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore.
Department of Infectious Diseases, Singapore General Hospital, Singapore.

Yee-Sin Leo (YS)

National Centre for Infectious Diseases, Singapore.
Department of Infectious Diseases, Tan Tock Seng Hospital, Singapore.
Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore.
Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
Saw Swee Hock School of Public Health, National University of Singapore, Singapore.

Laurent Renia (L)

ASTAR Infectious Diseases Labs, Agency for Science, Technology and Research, Singapore.
Singapore Immunology Network, Agency for Science, Technology and Research, Singapore.

Antonio Bertoletti (A)

Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore.

Lisa F P Ng (LFP)

ASTAR Infectious Diseases Labs, Agency for Science, Technology and Research, Singapore.
Singapore Immunology Network, Agency for Science, Technology and Research, Singapore.

David Chien Lye (DC)

National Centre for Infectious Diseases, Singapore.
Department of Infectious Diseases, Tan Tock Seng Hospital, Singapore.
Lee Kong Chian School of Medicine, Nanyang Technological University, Singapore.
Yong Loo Lin School of Medicine, National University of Singapore, Singapore.

Lin-Fa Wang (LF)

Programme in Emerging Infectious Diseases, Duke-NUS Medical School, Singapore.
SingHealth Duke-NUS Global Health Institute, Singapore.

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