Evidence map›Paper›PMID 39640868›Full record

ArticleWellcome open research2023

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.

John Kimotho, Yiakon Sein, Shahin Sayed, Reena Shah, Kennedy Mwai, Mansoor Saleh, Perpetual Wanjiku, Jedidah Mwacharo, James Nyagwange, Henry Karanja and 18 more

Abstract read
In one paragraph

Article in Wellcome open research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

28 authors.

John KimothoKEMRI-Wellcome Trust Research Programme, KILIFI, Coast, 230-80108, Kenya.ORCID https://orcid.org/0000-0002-4843-9958
Yiakon SeinKEMRI-Wellcome Trust Research Programme, KILIFI, Coast, 230-80108, Kenya.ORCID https://orcid.org/0000-0002-6448-672X
Shahin SayedAga Khan University Hospital, 3rd Parklands Avenue, Nairobi, 30270 - 00100, Kenya.
Reena ShahAga Khan University Hospital, 3rd Parklands Avenue, Nairobi, 30270 - 00100, Kenya.ORCID https://orcid.org/0000-0003-1729-5012
Kennedy MwaiKEMRI-Wellcome Trust Research Programme, KILIFI, Coast, 230-80108, Kenya.ORCID https://orcid.org/0000-0002-7757-7516
Mansoor SalehAga Khan University Hospital, 3rd Parklands Avenue, Nairobi, 30270 - 00100, Kenya.
Perpetual WanjikuKEMRI-Wellcome Trust Research Programme, KILIFI, Coast, 230-80108, Kenya.ORCID https://orcid.org/0000-0001-9293-0181
Jedidah MwacharoKEMRI-Wellcome Trust Research Programme, KILIFI, Coast, 230-80108, Kenya.
James NyagwangeKEMRI-Wellcome Trust Research Programme, KILIFI, Coast, 230-80108, Kenya.ORCID https://orcid.org/0000-0001-5430-6011
Henry KaranjaKEMRI-Wellcome Trust Research Programme, KILIFI, Coast, 230-80108, Kenya.ORCID https://orcid.org/0000-0002-8249-6833
Bernadette KutimaKEMRI-Wellcome Trust Research Programme, KILIFI, Coast, 230-80108, Kenya.ORCID https://orcid.org/0000-0001-6823-4071
John N GitongaKEMRI-Wellcome Trust Research Programme, KILIFI, Coast, 230-80108, Kenya.ORCID https://orcid.org/0000-0001-6482-9107
Daisy MugoKEMRI-Wellcome Trust Research Programme, KILIFI, Coast, 230-80108, Kenya.
Ann KaranuAga Khan University Hospital, 3rd Parklands Avenue, Nairobi, 30270 - 00100, Kenya.
Linda MorangaKEMRI-Wellcome Trust Research Programme, KILIFI, Coast, 230-80108, Kenya.ORCID https://orcid.org/0009-0006-7529-3639
Viviane OluochAga Khan University Hospital, 3rd Parklands Avenue, Nairobi, 30270 - 00100, Kenya.
Jasmit ShahAga Khan University Hospital, 3rd Parklands Avenue, Nairobi, 30270 - 00100, Kenya.
Julius MutisoAga Khan University Hospital, 3rd Parklands Avenue, Nairobi, 30270 - 00100, Kenya.
Alfred MburuAga Khan University Hospital, 3rd Parklands Avenue, Nairobi, 30270 - 00100, Kenya.
Zaitun NnekaAga Khan University Hospital, 3rd Parklands Avenue, Nairobi, 30270 - 00100, Kenya.
Peter BettiAga Khan University Hospital, 3rd Parklands Avenue, Nairobi, 30270 - 00100, Kenya.ORCID https://orcid.org/0009-0002-0914-4695
Wanzila Usyu MutindaPwani University, KILIFI, 230-80108, Kenya.ORCID https://orcid.org/0000-0002-9212-0856
Abdirahman Issak AbdiKEMRI-Wellcome Trust Research Programme, KILIFI, Coast, 230-80108, Kenya.ORCID https://orcid.org/0000-0001-7989-2125
Philip BejonKEMRI-Wellcome Trust Research Programme, KILIFI, Coast, 230-80108, Kenya.ORCID https://orcid.org/0000-0002-2135-7549
Lynette Isabella Ochola-OyierKEMRI-Wellcome Trust Research Programme, KILIFI, Coast, 230-80108, Kenya.
George M WarimweKEMRI-Wellcome Trust Research Programme, KILIFI, Coast, 230-80108, Kenya.ORCID https://orcid.org/0000-0002-4911-6333
Eunice W NduatiKEMRI-Wellcome Trust Research Programme, KILIFI, Coast, 230-80108, Kenya.ORCID https://orcid.org/0000-0001-7578-3095
Francis M NdunguKEMRI-Wellcome Trust Research Programme, KILIFI, Coast, 230-80108, Kenya.ORCID https://orcid.org/0000-0002-8977-0030

Funding

EPA EP-C-15-003Wellcome Trust
6 · The paper itself

Abstract

Background: Given 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. Methods: We 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. Results: Rates 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 (p<0.01) and were subsequently maintained for six months without significant decay (p>0.99). Similarly, antibody-neutralising potencies peaked at day 28 (p<0.01) but declined by three-fold, six months after COVID-19 diagnosis (p<0.01). Binding antibody levels were highly correlated with neutralising antibody potencies at all the time points analysed (r>0.60, p<0.01). Levels and potencies of binding and neutralising antibodies increased with disease severity. Conclusions: Most 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.

Indexed as

binding-antibodiesCOVID-19Kenyakineticsnatural infectionneutralizing antibodiesSARS-CoV-2sub-Saharan Africa

Identifiers

PMID39640868
PMCPMC11617823

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Registered trials

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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.