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

Abstract Background Tuberculosis (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-ret...

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Main Authors: Tom Sumner, Rebecca A. Clark, Tomos O. Prys-Jones, Roel Bakker, Gavin Churchyard, Richard G. White
Format: Article
Language:English
Published: BMC 2025-07-01
Series:BMC Infectious Diseases
Subjects:
Online Access:https://doi.org/10.1186/s12879-025-11249-y
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author Tom Sumner
Rebecca A. Clark
Tomos O. Prys-Jones
Roel Bakker
Gavin Churchyard
Richard G. White
author_facet Tom Sumner
Rebecca A. Clark
Tomos O. Prys-Jones
Roel Bakker
Gavin Churchyard
Richard G. White
author_sort Tom Sumner
collection DOAJ
description Abstract Background Tuberculosis (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. Methods Using 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. Results For 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. Conclusions Our 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.
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spelling doaj-art-478ffec54d2549adbc40aedfa87ae0282025-08-20T03:45:24ZengBMCBMC Infectious Diseases1471-23342025-07-0125111010.1186/s12879-025-11249-yThe delivery of new tuberculosis vaccines to people living with HIV – when to vaccinate?Tom Sumner0Rebecca A. Clark1Tomos O. Prys-Jones2Roel Bakker3Gavin Churchyard4Richard G. White5TB Modelling Group and TB Centre, London School of Hygiene and Tropical MedicineTB Modelling Group and TB Centre, London School of Hygiene and Tropical MedicineTB Modelling Group and TB Centre, London School of Hygiene and Tropical MedicineTB Modelling Group and TB Centre, London School of Hygiene and Tropical MedicineThe Aurum InstituteTB Modelling Group and TB Centre, London School of Hygiene and Tropical MedicineAbstract Background Tuberculosis (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. Methods Using 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. Results For 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. Conclusions Our 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.https://doi.org/10.1186/s12879-025-11249-yTuberculosisVaccinesHIVModelingAnti-retroviral therapy
spellingShingle Tom Sumner
Rebecca A. Clark
Tomos O. Prys-Jones
Roel Bakker
Gavin Churchyard
Richard G. White
The delivery of new tuberculosis vaccines to people living with HIV – when to vaccinate?
BMC Infectious Diseases
Tuberculosis
Vaccines
HIV
Modeling
Anti-retroviral therapy
title The delivery of new tuberculosis vaccines to people living with HIV – when to vaccinate?
title_full The delivery of new tuberculosis vaccines to people living with HIV – when to vaccinate?
title_fullStr The delivery of new tuberculosis vaccines to people living with HIV – when to vaccinate?
title_full_unstemmed The delivery of new tuberculosis vaccines to people living with HIV – when to vaccinate?
title_short The delivery of new tuberculosis vaccines to people living with HIV – when to vaccinate?
title_sort delivery of new tuberculosis vaccines to people living with hiv when to vaccinate
topic Tuberculosis
Vaccines
HIV
Modeling
Anti-retroviral therapy
url https://doi.org/10.1186/s12879-025-11249-y
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