Evidence map›Paper›PMID 42611920›Full record

ArticlePLOS global public health2026

Trends and patterns of varicella zoster virus infection in Kilifi: A population-based serosurvey.

Antipa K Sigilai, Caroline N Mburu, Rose Selim, Rose Ombati, Donald Akech, Boniface Karia, James Tuju, Gaby P Smits, van Gageldonk P G M, Fiona van der Klis and 3 more

Abstract read
In one paragraph

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

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0citing papers in PubMed
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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

13 authors.

Antipa K SigilaiKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.ORCID https://orcid.org/0000-0003-1185-3677
Caroline N MburuKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.ORCID https://orcid.org/0000-0001-6362-3537
Rose SelimKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.ORCID https://orcid.org/0000-0001-6969-167X
Rose OmbatiKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
Donald AkechKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
Boniface KariaKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.ORCID https://orcid.org/0000-0003-0875-8935
James TujuKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
Gaby P SmitsCentre for Immunology of Infectious Diseases and Vaccines, National Institute of Public Health, and the Environment (RIVM), Bilthoven, The Netherlands.
van Gageldonk P G MCentre for Immunology of Infectious Diseases and Vaccines, National Institute of Public Health, and the Environment (RIVM), Bilthoven, The Netherlands.
Fiona van der KlisCentre for Immunology of Infectious Diseases and Vaccines, National Institute of Public Health, and the Environment (RIVM), Bilthoven, The Netherlands.
E Wangeci KaguciaKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
J Anthony G ScottKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
Adetifa I M OKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.

Funding

Bill & Melinda Gates Foundation INV-039626Wellcome Trust
6 · The paper itself

Abstract

There is limited epidemiologic data on varicella zoster virus (VZV) infections from low- and middle-income countries including Kenya. We aimed to describe the seroepidemiology of VZV in Kilifi, Kenya, where varicella vaccine is not included in the national infant immunization program, in order to generate evidence to inform vaccine policy. We conducted a retrospective serosurvey utilizing archived plasma and serum samples from cross-sectional population-based serosurveys conducted within the Kilifi Health and Demographic Surveillance System between 2009 and 2021. We assayed immunoglobulin G (IgG) for VZV using a validated Luminex multiplex immunoassay and applied a seropositivity cutoff of ≥0.26 International Units per millilitre (IU/mL), as determined by the assay developer. We calculated Bayesian-adjusted age-specific seroprevalence and tested differences in seroprevalence between groups using Chi square. We used a multivariable logistic regression model to estimate associations with VZV IgG antibody seropositivity. We fitted an age-dependent catalytic model to estimate the force of infection (FOI) in children aged 0.5-4, 5-9 and 10-14 years. A total of 2639 samples from children aged <15 years and 546 samples from persons aged ≥15 years were tested. The overall population-weighted seroprevalence of VZV IgG antibodies among children aged 0-14 years was 38.4% (95% CI 27.5-49.5). Age-specific seroprevalence rose from 13.3% (95% CI 5.8-21.6) in children aged 0-4 years to 60.9% (95% CI 45.0-76.2) in those aged 10-14 years. Survey year and age were associated with VZV IgG antibody seropositivity. Children aged 5-9 years had the highest FOI (0.098; 95% CI 0.077-0.120) per susceptible year while mean age of infection was 24.3 years (95% CrI 17.6-30.1). Approximately 40% of individuals entering adulthood in Kenya remain susceptible to VZV infection, suggesting a substantial and underappreciated risk of severe VZV disease in older population including pregnant women. An infant varicella immunization program might avert disease across both paediatric and adult populations.

Identifiers

PMID42611920
PMCPMC13484961

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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.