Mycobacterium tuberculosis: Pathogenesis and therapeutic targets

被引:17
|
作者
Yang, Jiaxing [1 ,2 ]
Zhang, Laiying [1 ,2 ]
Qiao, Wenliang [3 ,4 ]
Luo, Youfu [1 ,2 ]
机构
[1] Sichuan Univ, West China Hosp, Ctr Infect Dis, Chengdu, Peoples R China
[2] Sichuan Univ, West China Hosp, State Key Lab Biotherapy, Chengdu, Peoples R China
[3] Sichuan Univ, West China Hosp, Dept Thorac Surg, Chengdu, Sichuan, Peoples R China
[4] Sichuan Univ, West China Hosp, Lung Canc Ctr, Chengdu, Sichuan, Peoples R China
来源
MEDCOMM | 2023年 / 4卷 / 05期
基金
中国国家自然科学基金;
关键词
biological targets; host-directed therapy; inhibitors; modulaters; Mycobacterium tuberculosis; pathogenesis; TUMOR-NECROSIS-FACTOR; MULTIDRUG-RESISTANT TUBERCULOSIS; CARRIER PROTEIN REDUCTASE; ENDOTHELIAL GROWTH-FACTOR; ACTIVATED RECEPTOR-GAMMA; AEROSOLIZED INTERFERON-ALPHA; PARA-AMINOSALICYLIC ACID; HUMAN DENDRITIC CELLS; DNA TOPOISOMERASE-I; PANTOTHENATE SYNTHETASE;
D O I
10.1002/mco2.353
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Tuberculosis (TB) remains a significant public health concern in the 21st century, especially due to drug resistance, coinfection with diseases like immunodeficiency syndrome (AIDS) and coronavirus disease 2019, and the lengthy and costly treatment protocols. In this review, we summarize the pathogenesis of TB infection, therapeutic targets, and corresponding modulators, including first-line medications, current clinical trial drugs and molecules in preclinical assessment. Understanding the mechanisms of Mycobacterium tuberculosis (Mtb) infection and important biological targets can lead to innovative treatments. While most antitubercular agents target pathogen-related processes, host-directed therapy (HDT) modalities addressing immune defense, survival mechanisms, and immunopathology also hold promise. Mtb's adaptation to the human host involves manipulating host cellular mechanisms, and HDT aims to disrupt this manipulation to enhance treatment effectiveness. Our review provides valuable insights for future anti-TB drug development efforts.
引用
收藏
页数:39
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