Controlled human infection with Mycobacterium tuberculosis: practical considerations for clinical trials
Chetan Seshadri, Flynn Jl, Pauline Maiello, Dirk Schnappinger, Robert J Wilkinson, Stephen B Gordon, Henry C Mwandumba, Kondwani C Jambo, et al. (13 authors)
The Lancet Microbe · 2026-01
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.
MeSH terms
- Tuberculosis
- Mycobacterium tuberculosis
- Medicine
- Clinical trial
- Intensive care medicine
- Tuberculosis vaccines
- Immunology
- Infectious disease (medical specialty)
- Disease
- Human pathogen
- Pulmonary tuberculosis
- Clinical research
- Pathogen
- Broad spectrum
- Virology