Cavitary tuberculosis: the gateway of disease transmission

被引:108
作者
Urbanowski, Michael E. [1 ,2 ,3 ]
Ordonez, Alvaro A. [1 ,2 ,4 ]
Ruiz-Bedoya, Camilo A. [1 ,2 ,4 ]
Jain, Sanjay K. [1 ,2 ,4 ]
Bishai, William R. [1 ,2 ,3 ]
机构
[1] Johns Hopkins Univ, Sch Med, Ctr TB Res, Baltimore, MD 21287 USA
[2] Johns Hopkins Univ, Sch Med, Ctr Infect & Inflammat Imaging Res, Baltimore, MD USA
[3] Johns Hopkins Univ, Sch Med, Dept Med, Baltimore, MD 21205 USA
[4] Johns Hopkins Univ, Sch Med, Dept Pediat, Baltimore, MD 21205 USA
基金
美国国家卫生研究院;
关键词
RESUSCITATION-PROMOTING FACTORS; DRUG-RESISTANT-TUBERCULOSIS; MONONUCLEAR EXUDATE CELLS; PULMONARY TUBERCULOSIS; MYCOBACTERIUM-TUBERCULOSIS; MOUSE MODEL; QUANTITATIVE ASSAY; HYDROLYTIC ENZYMES; SURGICAL-TREATMENT; HIGH-RESOLUTION;
D O I
10.1016/S1473-3099(20)30148-1
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Tuberculosis continues to be a major threat to global health. Cavitation is a dangerous consequence of pulmonary tuberculosis associated with poor outcomes, treatment relapse, higher transmission rates, and development of drug resistance. However, in the antibiotic era, cavities are often identified as the most extreme outcome of treatment failure and are one of the least-studied aspects of tuberculosis. We review the epidemiology, clinical features, and concurrent standards of care for individuals with cavitary tuberculosis. We also discuss developments in the understanding of tuberculosis cavities as dynamic physical and biochemical structures that interface the host response with a unique mycobacterial niche to drive tuberculosis-associated morbidity and transmission. Advances in preclinical models and non-invasive imaging can provide valuable insights into the drivers of cavitation. These insights will guide the development of specific pharmacological interventions to prevent cavitation and improve lung function for individuals with tuberculosis.
引用
收藏
页码:E117 / E128
页数:12
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