Evidence map›Paper›PMID 40597701›Full record

ArticleBMC infectious diseases2025

The delivery of new tuberculosis vaccines to people living with HIV - when to vaccinate?

Tom Sumner, Rebecca A Clark, Tomos O Prys-Jones, Roel Bakker, Gavin Churchyard, Richard G White

Abstract read
In one paragraph

Article in BMC infectious diseases, 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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0citing papers 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

The trial behind it

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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

6 authors.

Tom SumnerTB Modelling Group and TB Centre, London School of Hygiene and Tropical Medicine, Keppel Street, London, UK. tom.sumner@lshtm.ac.uk.
Rebecca A ClarkTB Modelling Group and TB Centre, London School of Hygiene and Tropical Medicine, Keppel Street, London, UK.
Tomos O Prys-JonesTB Modelling Group and TB Centre, London School of Hygiene and Tropical Medicine, Keppel Street, London, UK.
Roel BakkerTB Modelling Group and TB Centre, London School of Hygiene and Tropical Medicine, Keppel Street, London, UK.
Gavin ChurchyardThe Aurum Institute, Johannesburg, 2041, South Africa.
Richard G WhiteTB Modelling Group and TB Centre, London School of Hygiene and Tropical Medicine, Keppel Street, London, UK.

Funding

Aurum Clinical Trials UnitUM1AI154463 · NIAID · AURUM INSTITUTE NPC · PI Gavin John Churchyard · 2021 to 2026
$8.1M
NIAID NIH HHS UM1 AI154463NIH and CRDF Global G-202303-69963
6 · The paper itself

Abstract

backgroundTuberculosis (TB) remains a major cause of morbidity and mortality in people living with HIV (PLHIV). New TB vaccines may help reduce this burden. There is limited data on the response to new TB vaccines in PLHIV and how this may vary with levels of immunosuppression and anti-retroviral therapy (ART). The potential interaction between vaccine efficacy and ART raises questions about the optimum timing of vaccination against TB in PLHIV.

methodsUsing a simple cumulative risk model, we compared the impact of different TB vaccination strategies for PLHIV. We compared the impact of vaccinating at linkage to HIV care, to the impact of vaccinating at ART initiation. We explored how the optimum timing of vaccination depends on characteristics of the vaccine and the ART program at an individual and population level.

resultsFor an individual, the optimum timing of vaccination against TB is at ART initiation unless the time to ART initiation is more than 6 months or if the reduction in vaccine efficacy when given prior to ART is small. At a population level, the proportion of PLHIV who initiate ART is a key determinate of the optimum strategy. If ART uptake is low, it would be better to vaccinate at linkage to HIV care, even if vaccine efficacy in ART naïve individuals is less than 50% of efficacy in individuals on ART.

conclusionsOur results suggest that the optimum timing of new TB vaccination for PLHIV will depend on the relative efficacy of vaccination in ART-naïve individuals vs. individuals on ART, and the uptake and timing of ART initiation. If vaccine efficacy is lower among ART-naïve individuals, improvements in HIV programs may help maximize the impact of new TB vaccines.

Indexed as

HIV InfectionsTuberculosisTuberculosis VaccinesAdultFemaleHumansMaleVaccinationVaccine EfficacyTuberculosis VaccinesAnti-retroviral therapyHIVModelingTuberculosisVaccines

Identifiers

PMID40597701
PMCPMC12217277

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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.