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Kinetics of naturally induced binding and neutralising anti-SARS-CoV-2 antibody levels and potencies among SARS-CoV-2 infected Kenyans with diverse grades of COVID-19 severity: an observational study

Abstract:
BackgroundGiven the low levels of coronavirus disease 2019 (COVID-19) vaccine coverage in sub-Saharan Africa (sSA), despite high levels of natural severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) exposures, strategies for extending the breadth and longevity of naturally acquired immunity are warranted. Designing such strategies will require a good understanding of naturally acquired immunity.MethodsWe measured whole-spike immunoglobulin G (IgG) and spike-receptor binding domain (RBD) total immunoglobulins (Igs) on 585 plasma samples collected longitudinally over five successive time points within six months of COVID-19 diagnosis in 309 COVID-19 patients. We measured antibody-neutralising potency against the wild-type (Wuhan) SARS-CoV-2 pseudovirus in a subset of 51 patients over three successive time points. Binding and neutralising antibody levels and potencies were then tested for correlations with COVID-19 severities.ResultsRates of seroconversion increased from day 0 (day of PCR testing) to day 180 (six months) (63.6% to 100 %) and (69.3 % to 97%) for anti-spike-IgG and anti-spike-RBD binding Igs, respectively. Levels of these binding antibodies peaked at day 28 (p0.99). Similarly, antibody-neutralising potencies peaked at day 28 (p0.60, pConclusionsMost COVID-19 patients generated SARS-CoV-2 specific binding antibodies that remained stable in the first six months of infection. However, the respective neutralising antibodies decayed three-fold by month-six of COVID-19 diagnosis suggesting that they are short-lived, consistent with what has been observed elsewhere in the world. Thus, regular vaccination boosters are required to sustain the high levels of anti-SARS-CoV-2 naturally acquired neutralising antibody potencies in our population.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.12688/wellcomeopenres.19414.2

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Author
ORCID:
0000-0002-4843-9958
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ORCID:
0000-0002-6448-672X
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ORCID:
0000-0003-1729-5012
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ORCID:
0000-0002-7757-7516


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Funder identifier:
https://ror.org/029chgv08


Publisher:
Taylor and Francis
Journal:
Wellcome Open Research More from this journal
Volume:
8
Pages:
350
Publication date:
2023-01-01
Acceptance date:
2024-11-26
DOI:
EISSN:
2398-502X
ISSN:
2398-502X
Pmid:
39640868


Language:
English
Keywords:
Source identifiers:
2496921
Deposit date:
2024-12-14
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