Evidence map›Paper›PMID 41959821›Full record

ArticlemedRxiv : the preprint server for health sciences2026

Timing of antiretroviral treatment initiation and seropositivity to measles virus among children living with HIV in rural Zambia.

Catherine G Sutcliffe, Saki Takahashi, Amanda A Finney, Mutinta Hamahuwa, Nkumbula Moyo, Amy K Winter, Hellen K Matakala, Mathias Muleka, Passwell Munachoonga, Francis Hamangaba and 2 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 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

12 authors.

Catherine G SutcliffeDepartment of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland USA.ORCID 0000-0001-8512-8326
Saki TakahashiDepartment of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland USA.
Amanda A FinneyDepartment of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland USA.
Mutinta HamahuwaMacha Research Trust, Choma, Zambia.
Nkumbula MoyoMacha Research Trust, Choma, Zambia.
Amy K WinterCollege of Public Health, University of Georgia, Athens, Georgia USA.ORCID 0000-0003-2737-7003
Hellen K MatakalaMacha Research Trust, Choma, Zambia.
Mathias MulekaMacha Research Trust, Choma, Zambia.
Passwell MunachoongaMacha Research Trust, Choma, Zambia.
Francis HamangabaMacha Research Trust, Choma, Zambia.
Philip E ThumaMacha Research Trust, Choma, Zambia.
William J MossDepartment of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland USA.

Funding

TransmissionU19AI089680 · NIAID · JOHNS HOPKINS UNIVERSITY · PI WILLIAM J MOSS · 2010 to 2026
$25.6M
The impact of early antiretroviral treatment initiation on measles immunity among children living with HIVR21AI152847 · NIAID · JOHNS HOPKINS UNIVERSITY · PI SUTCLIFFE, CATHERINE GAYLE · 2021 to 2022
$375k
NCHHSTP CDC HHS U2G PS001930NIAID NIH HHS R21 AI152847NIAID NIH HHS U19 AI089680
6 · The paper itself

Abstract

Background: Combination antiretroviral therapy (cART) reduces morbidity among children living with HIV (CHIV) but does not restore measles immunity. Many CHIV now initiate cART before measles vaccination but the impact on measles-specific immunity is not understood. This study compared measles antibodies between CHIV initiating cART before and after 9 months of age in Zambia. Methods: This retrospective study was nested within an open cohort study of CHIV and community-based malaria studies in Macha, Zambia conducted from 2007-2020. Samples were tested for measles IgG antibodies from CHIV defined by age at cART initiation (aged 0-8, 9-23, and 24-59 months) and age-matched community-based controls. A cross-sectional analysis compared antibody concentrations between CHIV groups after 6-12 months of cART and aged >12 months and controls. A longitudinal analysis evaluated antibody trajectories from 9 months of age through 48 months of cART and during the 2010-11 measles outbreak. Results: In the cross-sectional analysis, 31.9% of 301 CHIV were seropositive after 6-12 of cART, with no significant difference by group (0-8: 30.8%; 9-23: 37.0%; 24-59 months: 26.6%). Within each CHIV group, the proportion seropositive was significantly lower than age-matched controls. Among 242 CHIV included in the longitudinal analysis, 46-56% had an antibody response, with an estimated time to seroreversion of 1.8-3.2 years. Among CHIV followed in 2010-11, 50% seroconverted or boosted; the estimated time to seroreversion was 2.1 years. Conclusions: Low levels of measles antibodies were found among CHIV, even when cART was started before 9 months of age, supporting a recommendation that CHIV, including infants, would benefit from revaccination.

Indexed as

Africaantiretroviral therapyHIVimmunitymeasles viruspediatrics

Identifiers

PMID41959821
PMCPMC13060988

What OpenQuestion holds

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Registered trials

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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.