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Controlled human infection with Mycobacterium tuberculosis: practical considerations for clinical trials

  • Chetan Seshadri
  • , JoAnne L. Flynn
  • , Pauline Maiello
  • , Dirk Schnappinger
  • , Robert J. Wilkinson
  • , Stephen B. Gordon
  • , Henry C. Mwandumba
  • , Kondwani C. Jambo
  • , Daniel F. Hoft
  • , Eric J. Rubin
  • , Euzebiusz Jamrozik
  • , Sarah M. Fortune
  • , James G. Kublin

Research output: Contribution to journalArticleResearchpeer-review

Abstract

Controlled human infection models (CHIMs) can accelerate vaccine development for infectious diseases. Mycobacterium tuberculosis is a human-adapted pathogen that is the leading infectious cause of death worldwide. M tuberculosis infection results in a spectrum of clinical outcomes that are incompletely modelled in animals. To date, the risks of infection, prolonged treatment, and sequelae related to CHIMs with M tuberculosis have been considered ethically unacceptable. However, recent advances in bacterial engineering have resulted in safe strains that could permit M tuberculosis CHIM studies with reduced risks. In this Personal View, we address the practical considerations for conducting a pulmonary M tuberculosis CHIM study. We summarise the ethical issues of M tuberculosis CHIM studies in tuberculosis-endemic and non-endemic settings; describe safety considerations, such as optimising the challenge dose and minimising risks to third parties; and outline and prioritise clinical, microbiological, immunological, and radiological endpoints that would render such a model useful for vaccine development.

Original languageEnglish
Article number101278
Number of pages10
JournalThe Lancet Microbe
Volume7
Issue number3
DOIs
Publication statusPublished - Mar 2026
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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