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The past, present and future of tuberculosis treatment / 浙江大学学报·医学版
Article in English | WPRIM (Western Pacific) | ID: wpr-971083
Responsible library: WPRO
ABSTRACT
Tuberculosis (TB) is an ancient infectious disease. Before the availability of effective drug therapy, it had high morbidity and mortality. In the past 100 years, the discovery of revolutionary anti-TB drugs such as streptomycin, isoniazid, pyrazinamide, ethambutol and rifampicin, along with drug combination treatment, has greatly improved TB control globally. As anti-TB drugs were widely used, multidrug-resistant (MDR) and extensively drug-resistant (XDR) strains of Mycobacterium tuberculosis emerged due to acquired genetic mutations, and this now presents a major problem for effective treatment. Genes associated with drug resistance have been identified, including katG mutations in isoniazid resistance, rpoB mutations in rifampin resistance, pncA mutations in pyrazinamide resistance, and gyrA mutations in quinolone resistance. The major mechanisms of drug resistance include loss of enzyme activity in prodrug activation, drug target alteration, overexpression of drug target, and overexpression of the efflux pump. During the disease process, Mycobacterium tuberculosis may reside in different microenvironments where it is expose to acidic pH, low oxygen, reactive oxygen species and anti-TB drugs, which can facilitate the development of non-replicating persisters and promote bacterial survival. The mechanisms of persister formation may include toxin-antitoxin (TA) modules, DNA protection and repair, protein degradation such as trans-translation, efflux, and altered metabolism. In recent years, the use of new anti-TB drugs, repurposed drugs, and their drug combinations has greatly improved treatment outcomes in patients with both drug-susceptible TB and MDR/XDR-TB. The importance of developing more effective drugs targeting persisters of Mycobacterium tuberculosis is emphasized. In addition, host-directed therapeutics using both conventional drugs and herbal medicines for more effective TB treatment should also be explored. In this article, we review historical aspects of the research on anti-TB drugs and discuss the current understanding and treatments of drug resistant and persistent tuberculosis to inform future therapeutic development.
Subject(s)

Full text: Available Health context: SDG3 - Health and Well-Being / Neglected Diseases / SDG3 - Target 3.3 End transmission of communicable diseases Health problem: Target 3.3: End transmission of communicable diseases / Neglected Diseases / Tuberculosis / Tuberculosis Database: WPRIM (Western Pacific) Main subject: Pyrazinamide / Rifampin / Tuberculosis / Tuberculosis, Multidrug-Resistant / Drug Resistance, Multiple, Bacterial / Isoniazid / Mutation / Mycobacterium tuberculosis / Antitubercular Agents Limits: Humans Language: English Journal: Journal of Zhejiang University. Medical sciences Year: 2023 Document type: Article
Full text: Available Health context: SDG3 - Health and Well-Being / Neglected Diseases / SDG3 - Target 3.3 End transmission of communicable diseases Health problem: Target 3.3: End transmission of communicable diseases / Neglected Diseases / Tuberculosis / Tuberculosis Database: WPRIM (Western Pacific) Main subject: Pyrazinamide / Rifampin / Tuberculosis / Tuberculosis, Multidrug-Resistant / Drug Resistance, Multiple, Bacterial / Isoniazid / Mutation / Mycobacterium tuberculosis / Antitubercular Agents Limits: Humans Language: English Journal: Journal of Zhejiang University. Medical sciences Year: 2023 Document type: Article
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