Completed Infection & Immunity Lungs & Breathing

Quadruple intervention against tuberculosis.

In plain English

AI plain-English summary

Tuberculosis treatment currently demands a six-month course of antibiotics, and this project tests whether a quadruple strategy—combining a shorter drug regime, vitamin D correction, a new vaccine, and early HIV therapy—can cut that time to one month and prevent new infections. Why this matters: Latent TB, where the bacterium lies dormant in the body, affects roughly a quarter of the world’s population. The standard six-month preventive treatment is often not completed, and vitamin D deficiency is common in TB patients, potentially weakening immune defences. HIV co-infection further complicates control. The research addresses these interconnected gaps by testing each intervention in parallel: a shorter drug regime, vitamin D supplementation, a novel vaccine combined with latent TB treatment, and early antiretroviral therapy in HIV-positive individuals. Potential impact: If successful, the work could transform TB control by making preventive treatment far more practical—reducing dropout rates, boosting immune responses, and cutting transmission. This would directly affect public health systems in high-burden settings, where TB remains a leading infectious killer, and could reduce the need for lengthy clinic visits and monitoring. The vaccine component, if effective, might also provide lasting protection beyond treatment. The project is applied and intervention-focused, with clear pathways to clinical implementation.

View original technical description
Research aims relate to the hypotheses above designed to support a quadruple intervention against tuberculosis as follows: 1. Treatment of latent TB (LTBI) with a multi-drug regime to reduce duration to one, instead of six, months 2. Correction of vitamin D deficiency that associates with TB 3. Vaccination against TB that can be combined with treatment for LTBI 4. Early initiation of antiretroviral therapy in HIV infected persons Aim 1 will compare a novel regime for the treatment of LT BI with the standard treatment of INH with safety as the primary, and immunological and metabolic changes as secondary endpoints. Aim 2 will survey for vitamin D deficiency amongst TB patients and those without active TB and to carry out a study to determine the efficacy and safety of supplementation. Aim 3 will monitor the immunological response to a novel vaccine after 6 months IPT or placebo treatment in patients with LTBI. Aim 4 will compare the restoration of M. tuberculosis sp ecific immune responses in persons who begin cART at a nadir CD4 < 100 with those who begin at a nadir between 300-350.

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Researchers

Robert Wilkinson (EPMC Awardee)

Related Research

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Original classification

Senior Research Fellowship Clinical Renewal

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