Evidence map›Paper›PMID 41162599›Full record

ArticleScientific reports2025

Characterising protective immune responses to SARS-CoV-2 in urban and rural Malawi between February 2021 and April 2022.

Mhairi J McCormack, Louis Banda, Stephen Kasenda, Ellen C Hughes, Lina Leonhard, Annie Mwale, Estelle McLean, Alison Price, Amelia Crampin, David Chaima and 4 more

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–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

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. 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

14 authors.

Mhairi J McCormack *MRC-University of Glasgow Centre for Virus Research, Glasgow, UK. m.mccormack.1@research.gla.ac.uk.
Louis Banda *Malawi Epidemiology and Intervention Research Unit (MEIRU), Lilongwe, Malawi.
Stephen Kasenda *Malawi Epidemiology and Intervention Research Unit (MEIRU), Lilongwe, Malawi.
Ellen C HughesMRC-University of Glasgow Centre for Virus Research, Glasgow, UK.
Lina LeonhardMRC-University of Glasgow Centre for Virus Research, Glasgow, UK.
Annie MwalePublic Health Institute of Malawi, Lilongwe, Malawi.
Estelle McLeanMalawi Epidemiology and Intervention Research Unit (MEIRU), Lilongwe, Malawi.
Alison PriceMalawi Epidemiology and Intervention Research Unit (MEIRU), Lilongwe, Malawi.
Amelia CrampinMalawi Epidemiology and Intervention Research Unit (MEIRU), Lilongwe, Malawi.
David ChaimaKamuzu University of Health Sciences (KUHeS), Blantyre, Malawi.
Abena S AmoahMalawi Epidemiology and Intervention Research Unit (MEIRU), Lilongwe, Malawi.
Tonney S NyirendaKamuzu University of Health Sciences (KUHeS), Blantyre, Malawi.
Antonia HoMRC-University of Glasgow Centre for Virus Research, Glasgow, UK.
Brian J WillettMRC-University of Glasgow Centre for Virus Research, Glasgow, UK.

Funding

Medical Research Council MC_UU_00034/6Wellcome Trust 217073/Z/19/Z
6 · The paper itself

Abstract

SARS-CoV-2 transmission in Malawi remains unclear due to high proportions of mild/asymptomatic infections and limited diagnostics. Existing seroprevalence studies in Malawi have primarily used convenience samples and enzyme-linked immunosorbent assays (ELISAs). We assessed SARS-CoV-2 neutralisation in a longitudinal Malawian population-based cohort, assessing protective immunity post-infection and vaccination. Sera were obtained from rural (Karonga, n = 958) and urban (Lilongwe, n = 918) based participants at three-monthly intervals (February 2021-April 2022). Neutralising antibodies against SARS-CoV-2 were measured using human immunodeficiency (HIV)-based pseudotype assays in HIV-uninfected participants, and vesicular stomatitis virus-based assays in HIV-infected participants and an HIV-uninfected subset. Nucleocapsid ELISAs identified vaccinated participants also infected. SARS-CoV-2 neutralisation profiles increased in complexity over time from rising vaccination coverage and emerging variants. Neutralising antibody prevalence was higher in Lilongwe than Karonga (68.1% (CI 63.5-72.4) vs. 45.4% (CI 41.6-49.3), Survey 4). Hybrid immune and solely vaccinated participants exhibited higher titres than those solely infected. Children < 15 years had the lowest neutralising antibody titres among infected (not vaccinated) participants. People living with HIV had lower neutralising responses than those HIV-uninfected, particularly post vaccination. We therefore recommend surveillance of children and people living with HIV as low neutralisation responses increase reinfection risk. COVID-19 vaccination should be prioritised for HIV-infected individuals.

Indexed as

COVID-19SARS-CoV-2AdolescentAdultAntibodies, NeutralizingAntibodies, ViralChildChild, PreschoolCOVID-19 VaccinesFemaleHIV InfectionsHumansLongitudinal StudiesMalawiMaleMiddle AgedAntibodies, NeutralizingAntibodies, ViralCOVID-19 VaccinesHIVLongitudinalMalawiNeutralising antibodySARS-CoV-2Seroepidemiology

Identifiers

PMID41162599
PMCPMC12572322

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.