» Articles » PMID: 29753789

Diverse Cavity Types and Evidence That Mechanical Action on the Necrotic Granuloma Drives Tuberculous Cavitation

Overview
Journal Am J Pathol
Publisher Elsevier
Specialty Pathology
Date 2018 May 14
PMID 29753789
Citations 15
Authors
Affiliations
Soon will be listed here.
Abstract

Effacement of normal lung parenchyma by cavities is an important sequela of pulmonary tuberculosis. Despite its clinical significance, the pathogenesis of tuberculous cavitation is poorly understood, with controversy as to whether the fundamental mechanism involves matrix depletion, lipid pneumonia, or mechanical factors. In this study, a repetitive aerosol infection model using Mycobacterium tuberculosis was used to generate cavities in 20 New Zealand white rabbits. Serial computed tomography was performed to monitor cavity progression over 14 weeks. Three-dimensional reconstructions were compiled for each time point, allowing comprehensive four-dimensional cavity mapping. Terminally, cavities were processed for histopathology. Cavities progressed rapidly from areas of consolidation, and often showed a pattern of explosive growth followed by gradual contraction. Cavities formed preferentially in the caudodorsal lung fields, and frequently were subpleural. Cavitation was associated invariably with necrosis. Histomorphology showed four distinct cavity types that provide mechanistic clues and insight on early cavity development. Our study shows that cavitation is a highly dynamic process with preferential formation at sites of high mechanical stress. These findings suggest a model for the pathogenesis of tuberculous cavitation in which mechanical stress acts on the necrotic granuloma to produce acute tears in structurally weakened tissue, with subsequent air trapping and cavity expansion.

Citing Articles

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.


Significance of changes in cavity after treatment in Mycobacterium avium complex pulmonary disease.

Kim J, Bae J, Hyung K, Lee I, Park H, Kim S Sci Rep. 2024; 14(1):21133.

PMID: 39256432 PMC: 11387760. DOI: 10.1038/s41598-024-71971-6.


Pharmacokinetic-pharmacodynamic modeling of tuberculosis time to positivity and colony-forming unit to assess the response to dose-ranging linezolid.

Simeon S, Garcia-Cremades M, Savic R, P Solans B Antimicrob Agents Chemother. 2024; 68(8):e0019024.

PMID: 39016594 PMC: 11323931. DOI: 10.1128/aac.00190-24.


Comparative pathology of experimental pulmonary tuberculosis in animal models.

Hunter L, Ruedas-Torres I, Agullo-Ros I, Rayner E, Salguero F Front Vet Sci. 2023; 10:1264833.

PMID: 37901102 PMC: 10602689. DOI: 10.3389/fvets.2023.1264833.


Polyclonal Hyperglobulinemia with Multiple Pulmonary Cysts and Nodules: Concerning the Mechanism Underlying Cyst Formation.

Ota T, Suzuki H, Kawabata Y, Hino T, Yanagawa N Intern Med. 2023; 63(2):277-282.

PMID: 37225481 PMC: 10864062. DOI: 10.2169/internalmedicine.1875-23.


References
1.
Cardona P . A spotlight on liquefaction: evidence from clinical settings and experimental models in tuberculosis. Clin Dev Immunol. 2011; 2011:868246. PMC: 3061317. DOI: 10.1155/2011/868246. View

2.
Belton M, Brilha S, Manavaki R, Mauri F, Nijran K, Hong Y . Hypoxia and tissue destruction in pulmonary TB. Thorax. 2016; 71(12):1145-1153. PMC: 5136721. DOI: 10.1136/thoraxjnl-2015-207402. View

3.
Urbanowski M, Ihms E, Bigelow K, Kubler A, Elkington P, Bishai W . Repetitive Aerosol Exposure Promotes Cavitary Tuberculosis and Enables Screening for Targeted Inhibitors of Extensive Lung Destruction. J Infect Dis. 2018; 218(1):53-63. PMC: 5989619. DOI: 10.1093/infdis/jiy127. View

4.
Walker N, Clark S, Oni T, Andreu N, Tezera L, Singh S . Doxycycline and HIV infection suppress tuberculosis-induced matrix metalloproteinases. Am J Respir Crit Care Med. 2012; 185(9):989-97. PMC: 3359940. DOI: 10.1164/rccm.201110-1769OC. View

5.
SWEANY H, SEILER H . The pathology and bacteriology of resected lesions in pulmonary tuberculosis. Dis Chest. 1956; 29(2):119-52. DOI: 10.1378/chest.29.2.119. View