Evidence map›Paper›PMID 35346184›Full record

ArticleBMC medicine2022

AstraZeneca COVID-19 vaccine induces robust broadly cross-reactive antibody responses in Malawian adults previously infected with SARS-CoV-2.

Marah G Chibwana, Thandeka Moyo-Gwete, Gaurav Kwatra, Jonathan Mandolo, Tandile Hermanaus, Thopisang Motlou, Nonkululeko Mzindle, Frances Ayres, Mphatso Chaponda, Godwin Tembo and 13 more

Open access · goldAbstract read
In one paragraph

Article in BMC medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.5field-weighted citation impact, top 9% 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.

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

15 citing papers in PubMed, 25 citations in OpenAlex.

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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

23 authors at 5 institutions in 4 countries.

Marah G Chibwana *Malawi-Liverpool-Wellcome Trust Clinical Research programme (MLW), Blantyre, Malawi.
Thandeka Moyo-Gwete *National Institute for Communicable Diseases of the National Health Laboratory Services, Johannesburg, South Africa.
Gaurav KwatraRespiratory and Meningeal Pathogens Research Unit, University of the Witwatersrand, Johannesburg, South Africa.
Jonathan MandoloMalawi-Liverpool-Wellcome Trust Clinical Research programme (MLW), Blantyre, Malawi.
Tandile HermanausNational Institute for Communicable Diseases of the National Health Laboratory Services, Johannesburg, South Africa.
Thopisang MotlouNational Institute for Communicable Diseases of the National Health Laboratory Services, Johannesburg, South Africa.
Nonkululeko MzindleNational Institute for Communicable Diseases of the National Health Laboratory Services, Johannesburg, South Africa.
Frances AyresNational Institute for Communicable Diseases of the National Health Laboratory Services, Johannesburg, South Africa.
Mphatso ChapondaMalawi-Liverpool-Wellcome Trust Clinical Research programme (MLW), Blantyre, Malawi.
Godwin TemboMalawi-Liverpool-Wellcome Trust Clinical Research programme (MLW), Blantyre, Malawi.
Percy MwenechanyaMalawi-Liverpool-Wellcome Trust Clinical Research programme (MLW), Blantyre, Malawi.
Ndaona MitoleMalawi-Liverpool-Wellcome Trust Clinical Research programme (MLW), Blantyre, Malawi.
Chisomo JassiMalawi-Liverpool-Wellcome Trust Clinical Research programme (MLW), Blantyre, Malawi.
Raphael Kamng'onaMalawi-Liverpool-Wellcome Trust Clinical Research programme (MLW), Blantyre, Malawi.
Louise AfranMalawi-Liverpool-Wellcome Trust Clinical Research programme (MLW), Blantyre, Malawi.
David MzinzaMalawi-Liverpool-Wellcome Trust Clinical Research programme (MLW), Blantyre, Malawi.
Henry C MwandumbaMalawi-Liverpool-Wellcome Trust Clinical Research programme (MLW), Blantyre, Malawi.
Stephen B GordonMalawi-Liverpool-Wellcome Trust Clinical Research programme (MLW), Blantyre, Malawi.
Khuzwayo JereMalawi-Liverpool-Wellcome Trust Clinical Research programme (MLW), Blantyre, Malawi.
Shabir MadhiRespiratory and Meningeal Pathogens Research Unit, University of the Witwatersrand, Johannesburg, South Africa.
Penny L MooreNational Institute for Communicable Diseases of the National Health Laboratory Services, Johannesburg, South Africa.
Robert S HeydermanNIHR Global Health Research Unit on Mucosal Pathogens, Research Department of Infection, Division of Infection and Immunity, University College London, London, UK.
Kondwani C JamboMalawi-Liverpool-Wellcome Trust Clinical Research programme (MLW), Blantyre, Malawi. Kondwani.Jambo@lstmed.ac.uk.ORCID 0000-0002-3195-2210
University of Liverpool · GBNational Health Laboratory Service · ZAChristian Medical College, Vellore · INUniversity College London · GBUniversity of the Witwatersrand · ZA

Funding

Medical Research Council MR/P020526/1Wellcome TrustWellcome Trust 206545/Z/17/Z
6 · The paper itself

Abstract

backgroundBinding and neutralising anti-Spike antibodies play a key role in immune defence against SARS-CoV-2 infection. Since it is known that antibodies wane with time and new immune-evasive variants are emerging, we aimed to assess the dynamics of anti-Spike antibodies in an African adult population with prior SARS-CoV-2 infection and to determine the effect of subsequent COVID-19 vaccination.

methodsUsing a prospective cohort design, we recruited adults with prior laboratory-confirmed mild/moderate COVID-19 in Blantyre, Malawi, and followed them up for 270 days (n = 52). A subset of whom subsequently received a single dose of the AstraZeneca COVID-19 vaccine (ChAdOx nCov-19) (n = 12). We measured the serum concentrations of anti-Spike and receptor-binding domain (RBD) IgG antibodies using a Luminex-based assay. Anti-RBD antibody cross-reactivity across SARS-CoV-2 variants of concern (VOC) was measured using a haemagglutination test. A pseudovirus neutralisation assay was used to measure neutralisation titres across VOCs. Ordinary or repeated measures one-way ANOVA was used to compare log10 transformed data, with p value adjusted for multiple comparison using Šídák's or Holm-Šídák's test.

resultsWe show that neutralising antibodies wane within 6 months post mild/moderate SARS-CoV-2 infection (30-60 days vs. 210-270 days; Log ID

conclusionsThese findings show that the AstraZeneca COVID-19 vaccine is an effective booster for waning cross-variant antibody immunity after initial priming with SARS-CoV-2 infection. The potency of hybrid immunity and its potential to maximise the benefits of COVID-19 vaccines needs to be taken into consideration when formulating vaccination policies in sub-Saharan Africa, where there is still limited access to vaccine doses.

Indexed as

COVID-19Viral VaccinesAntibody FormationCOVID-19 SerotherapyCOVID-19 VaccinesHumansImmunization, PassiveProspective StudiesSARS-CoV-2COVID-19 VaccinesViral VaccinesAntibodiesAstraZeneca COVID-19 vaccineRBDSARS-CoV-2SpikeVOC

Identifiers

PMID35346184
PMCPMC8958481
OpenAlexW4220869197

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.