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分枝杆菌对化疗试剂和宿主防御策略的颠覆:结核病药物研发面临的挑战

Mycobacterial subversion of chemotherapeutic reagents and host defense tactics: challenges in tuberculosis drug development.

作者信息

Nguyen Liem, Pieters Jean

机构信息

Department of Molecular Biology and Microbiology, School of Medicine, Case Western Reserve University, Cleveland, Ohio 44106, USA.

出版信息

Annu Rev Pharmacol Toxicol. 2009;49:427-53. doi: 10.1146/annurev-pharmtox-061008-103123.

Abstract

Recent worldwide emergence of multidrug-resistant and extensively drug-resistant tuberculosis is threatening to destabilize tuberculosis control programs and urging global attention to the development of alternative tuberculosis therapies. Major roadblocks limiting the development and effectiveness of new drugs to combat tuberculosis are the profound innate resistance of Mycobacterium tuberculosis to host defense mechanisms as well as its intrinsic tolerance to chemotherapeutic reagents. The triangle of interactions among the pathogen, the host responses, and the drugs used to cure the disease are critical for the outcome of tuberculosis. We must better understand this three-way interaction in order to develop drugs that are able to kill the bacillus in the most effective way and minimize the emergence of drug resistance. Here we review our recent understanding of the molecular basis underlying intrinsic antibiotic resistance and survival tactics of M. tuberculosis. This knowledge may help to reveal current targets for the development of novel antituberculosis drugs.

摘要

近年来,耐多药和广泛耐药结核病在全球范围内的出现,正威胁着结核病控制项目的稳定,并促使全球关注替代结核病治疗方法的开发。限制新型抗结核药物研发及其有效性的主要障碍是结核分枝杆菌对宿主防御机制具有极强的固有抗性,以及其对化疗试剂的内在耐受性。病原体、宿主反应和用于治疗疾病的药物之间的相互作用三角对于结核病的治疗结果至关重要。为了开发能够以最有效方式杀死杆菌并最大限度减少耐药性出现的药物,我们必须更好地理解这种三方相互作用。在此,我们综述了我们对结核分枝杆菌固有抗生素抗性和生存策略的分子基础的最新认识。这些知识可能有助于揭示新型抗结核药物开发的当前靶点。

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