» Articles » PMID: 16441433

Characterization of the Tuberculous Granuloma in Murine and Human Lungs: Cellular Composition and Relative Tissue Oxygen Tension

Overview
Journal Cell Microbiol
Publisher Wiley
Date 2006 Jan 31
PMID 16441433
Citations 198
Authors
Affiliations
Soon will be listed here.
Abstract

The granulomatous reaction is the hallmark of the host response to infection with Mycobacterium tuberculosis. Despite its apparent importance to host defence against the tubercle bacillus, the granulomatous response remains to be completely defined. The present study used histological, immunohistochemical and flow-cytometric analyses to characterize pulmonic granulomatous tissues of tuberculous mice and humans. The kinetics of recruitment of neutrophils, macrophages, dendritic cells, and T and B lymphocytes into the lungs of mice infected aerogenically with the virulent Erdman strain of M. tuberculosis was evaluated in detail in both the acute and persistent phase of infection. A hypoxia-sensing compound based on the 2-nitroimidazole structure (EF5), together with immunohistochemical studies targeting endothelial cells were used to examine the relative oxygen tension in tuberculous granulomatous tissues in mice. The results have provided evidence that: (i) the granulomatous tissues are a highly organized structure whose formation is regulated by orderly recruitment of specific immune cells exhibiting distinct spatial relationship with one another; (ii) the granulomatous reaction, at least in the mouse, may represent an exaggerated response to the tubercle bacillus that can play a role in the development of immunopathology; (iii) B lymphoid aggregates are a prominent feature in both murine and human granulomatous tissues, although the immune cells that are most prominently associated with these clusters vary among the two species; (iv) murine tuberculous granulomatous tissues are relatively aerobic, suggesting that mouse models of persistent tuberculosis may not be suitable for the study of any hypoxic response of M. tuberculosis.

Citing Articles

The importance of inflammatory biomarkers in detecting and managing latent tuberculosis infection.

Gunasekaran H, Ranganathan U, Bethunaickan R Front Immunol. 2025; 16:1538127.

PMID: 39981231 PMC: 11839662. DOI: 10.3389/fimmu.2025.1538127.


Spatial transcriptomic analysis of HIV and tuberculosis coinfection in a humanized mouse model reveals specific transcription patterns, immune responses and early morphological alteration signaling.

Adduri S, Bohorquez J, Adejare O, Rincon D, Tucker T, Konduru N bioRxiv. 2025; .

PMID: 39975088 PMC: 11838271. DOI: 10.1101/2025.01.29.635571.


Understanding the development of tuberculous granulomas: insights into host protection and pathogenesis, a review in humans and animals.

Lyu J, Narum D, Baldwin S, Larsen S, Bai X, Griffith D Front Immunol. 2024; 15:1427559.

PMID: 39717773 PMC: 11663721. DOI: 10.3389/fimmu.2024.1427559.


The rs11684747 and rs55790676 SNPs of ADAM17 influence tuberculosis susceptibility and plasma levels of TNF, TNFR1, and TNFR2.

Choreno-Parra J, Ramon-Luing L, Castillejos M, Ortega-Martinez E, Tapia-Garcia A, Matias-Martinez M Front Microbiol. 2024; 15:1392782.

PMID: 38881671 PMC: 11177089. DOI: 10.3389/fmicb.2024.1392782.


Mycobacterium tuberculosis produces D-serine under hypoxia to limit CD8 T cell-dependent immunity in mice.

Cheng H, Ji Z, Wang Y, Li S, Tang T, Wang F Nat Microbiol. 2024; 9(7):1856-1872.

PMID: 38806671 PMC: 11222154. DOI: 10.1038/s41564-024-01701-1.