Evidence map›Paper›PMID 41073594›Full record

ArticleScientific reports2025

Long-term dynamics of cytomegalovirus-specific antibodies in a longitudinal cohort of children followed up for the first decade of life.

Maureen W Mburu, Mercy S Safari, Timothy O Makori, Elijah T Gicheru, Omar K Nyawa, Timothy Chege Kuria, Deirdre J Foley, Charles J Sande

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. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Maureen W Mburu *KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
Mercy S Safari *KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
Timothy O Makori *KEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
Elijah T GicheruKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
Omar K NyawaKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya.
Timothy Chege KuriaDepartment of Biology, Division of Genetics, Nikolaus-Fiebiger-Centre for Molecular Medicine, Friedrich-Alexander-Universität Erlangen- Nürnberg (FAU), Erlangen, Germany.
Deirdre J FoleyDepartment of Paediatric Infectious Disease, Children's Health Ireland at Crumlin, Dublin, Ireland.
Charles J SandeKEMRI-Wellcome Trust Research Programme, Kilifi, Kenya. csande@kemri-wellcome.org.

Funding

Wellcome TrustWellcome Trust WT105882MA
6 · The paper itself

Abstract

Cytomegalovirus (CMV) causes infections that last a lifetime and are primarily contracted in childhood. Congenital transmitted CMV is associated with severe neurological sequelae and can cause life-threatening disease in immunocompromised individuals. Although antibodies are generally presumed to correlate with protection, their long-term dynamics remain poorly understood. We aimed to determine the longevity of CMV-specific antibodies in a low-income setting in Kilifi County, Kenya. To track long-term antibody dynamics, we conducted longitudinal surveillance of annually collected serum samples and assayed for antibodies against the CMV tegument phosphoprotein (pp150). The duration of effective immunity against re-infection was estimated using piecewise regression modelling. Serum antibody to CMV was measured in 123 children recruited within the first five years of life and sampled annually over a median of 10 years (range: 7-14). Antibodies to the CMV pp150 showed a cyclic trend of acquisition and loss at the population level. Individually, we observed early antibody acquisition, followed by decline and rebound. Regression analysis identified a 7.57-year inflection point in antibody trajectories, marking a transition from waning to re-accumulation - potentially reflecting natural boosting events in a population where CMV infection occurs early in life. The data show a clear pattern of early natural infection, followed by repeated patterns of antibody acquisition, loss, and re-acquisition over the first decade and a half of life.

Indexed as

Antibodies, ViralCytomegalovirusCytomegalovirus InfectionsAdolescentChildChild, PreschoolFemaleHumansInfantKenyaLongitudinal StudiesMaleAntibodies, ViralAntibody kineticsChildrenCytomegalovirus (CMV)Longitudinal analysisSub-Saharan africa

Identifiers

PMID41073594
PMCPMC12514181

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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.