Heterogeneity in tuberculosis pathology, microenvironments and therapeutic responses

Summary Tuberculosis (TB) lesions are extremely complex and dynamic. Here, we review the multiple types and fates of pulmonary lesions that form following infection by Mycobacterium tuberculosis and the impact of this spatial and temporal heterogeneity on the bacteria they harbor. The diverse immuno...

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Published inImmunological reviews Vol. 264; no. 1; pp. 288 - 307
Main Authors Lenaerts, Anne, Barry III, Clifton E., Dartois, Véronique
Format Journal Article
LanguageEnglish
Published England Blackwell Publishing Ltd 01.03.2015
BlackWell Publishing Ltd
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Summary:Summary Tuberculosis (TB) lesions are extremely complex and dynamic. Here, we review the multiple types and fates of pulmonary lesions that form following infection by Mycobacterium tuberculosis and the impact of this spatial and temporal heterogeneity on the bacteria they harbor. The diverse immunopathology of granulomas and cavities generates a plethora of microenvironments to which M. tuberculosis bacilli must adapt. This in turn affects the replication, metabolism, and relative density of bacterial subpopulations, and consequently their respective susceptibility to chemotherapy. We outline recent developments that support a paradigm shift in our understanding of lesion progression. The simple model according to which lesions within a single individual react similarly to the systemic immune response no longer prevails. Host‐pathogen interactions within lesions are a dynamic process, driven by subtle and local differences in signaling pathways, resulting in diverging trajectories of lesions within a single host. The spectrum of TB lesions is a continuum with a large overlap in the lesion types found in latently infected and active TB patients. We hope this overview will guide TB researchers in the design, choice of read‐outs, and interpretation of future studies in the search for predictive biomarkers and novel therapies.
Bibliography:NIH/NIAID IDIQ Contract - No. HHSN272201000009I/01
TB Drug Accelerator program of the Bill and Melinda Gates Foundation
Intramural Research Program of the NIH, NIAID (Clifton Barry) and NIH - No. 1R01AI111967-01; No. 1R01AI106398-01
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Video podcast available Go to http://www.immunologicalreviews.com to watch an interview with Guest Editor Carl Nathan.
This article is a part of a series of reviews covering Tuberculosis appearing in Volume 264 of Immunological Reviews.
ISSN:0105-2896
1600-065X
DOI:10.1111/imr.12252