Evidence map›Paper›PMID 41748603›Full record

ArticleNPJ vaccines2026

Pooled analysis of PCV13 efficacy from controlled human infection trials in Malawi and the UK.

Evaristar Kudowa, Godwin Tembo, Anthony E Chirwa, Tarsizio Chikaonda, Alfred Muyaya, Lumbani Makhaza, Edna Nsomba, Bridgette Galafa, Faith Thole, John Ndaferankhande and 13 more

Abstract read
In one paragraph

Article in NPJ vaccines, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Evaristar KudowaMalawi Liverpool Wellcome Research Programme, Blantyre, Malawi. ekudowa@mlw.mw.
Godwin TemboMalawi Liverpool Wellcome Research Programme, Blantyre, Malawi.
Anthony E ChirwaMalawi Liverpool Wellcome Research Programme, Blantyre, Malawi.
Tarsizio ChikaondaMalawi Liverpool Wellcome Research Programme, Blantyre, Malawi.
Alfred MuyayaMalawi Liverpool Wellcome Research Programme, Blantyre, Malawi.
Lumbani MakhazaMalawi Liverpool Wellcome Research Programme, Blantyre, Malawi.
Edna NsombaMalawi Liverpool Wellcome Research Programme, Blantyre, Malawi.
Bridgette GalafaMalawi Liverpool Wellcome Research Programme, Blantyre, Malawi.
Faith TholeMalawi Liverpool Wellcome Research Programme, Blantyre, Malawi.
John NdaferankhandeMalawi Liverpool Wellcome Research Programme, Blantyre, Malawi.
Lorensio ChimgonekoMalawi Liverpool Wellcome Research Programme, Blantyre, Malawi.
Neema TotoMalawi Liverpool Wellcome Research Programme, Blantyre, Malawi.
Dingase DulaMalawi Liverpool Wellcome Research Programme, Blantyre, Malawi.
Ben MortonLiverpool School of Tropical Medicine, Liverpool, UK.
Shaun H PenningtonLiverpool School of Tropical Medicine, Liverpool, UK.
Angela Hyder-WrightLiverpool School of Tropical Medicine, Liverpool, UK.
Andrea M CollinsLiverpool School of Tropical Medicine, Liverpool, UK.
Elena MitsiLiverpool School of Tropical Medicine, Liverpool, UK.
Daniela M FerreiraLiverpool School of Tropical Medicine, Liverpool, UK.
Stephen B GordonMalawi Liverpool Wellcome Research Programme, Blantyre, Malawi. sgordon@mlw.mw.
Marc Y R HenrionMalawi Liverpool Wellcome Research Programme, Blantyre, Malawi. mhenrion@mlw.mw.
MARVELS
EHPC consortia

Funding

Bill and Melinda Gates Foundation OPP1117728Medical Research Council MR/K01188X/1Wellcome Trust 211433
6 · The paper itself

Abstract

We conducted the first pooled analysis of two randomised controlled vaccine trials on experimental pneumococcal serotype 6B carriage, registered in Malawi (PACTR202008503507113) and the UK (ISRCTN45340436). This post-hoc exploratory study examined the sex-based differences in carriage, vaccine efficacy and vaccine-induced responses. PCV-13 reduced colonisation by 76% (p < 0.001) with non-significant interaction by sex (RR = 1.549, p = 0.413). Females showed a higher carriage rate than males (28% vs. 19%, p = 0.066). Baseline anti-6B Capsular Polysaccharide Immunoglobulin G (IgG) titres were higher in females, significantly in Malawi (2.62 µg/ml vs males 2.05 µg/ml, p = 0.015). Post-vaccination titres did not differ by sex. The pooled fold change in IgG pre-post vaccination, was higher in vaccinated females (5.47 vs 3.30, p = 0.053). This analysis demonstrates the utility and challenges of integrating CHIM data between diverse settings to evaluate vaccine efficacy, describe inter-setting differences, investigate biological and immunological factors influencing protection against pneumococcal carriage and ultimately inform future vaccine development strategies.

Identifiers

PMID41748603
PMCPMC13176328

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.