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揭示 对贝达喹啉、德拉马尼和普托马尼耐药性不断加剧的困境和缺陷

Unraveling Dilemmas and Lacunae in the Escalating Drug Resistance of to Bedaquiline, Delamanid, and Pretomanid.

机构信息

Infectious Diseases Division, CSIR - Indian Institute of Integrative Medicine, Jammu-180001, India.

Academy of Scientific and Innovative Research (AcSIR), Ghaziabad-201002, India.

出版信息

J Med Chem. 2024 Feb 22;67(4):2264-2286. doi: 10.1021/acs.jmedchem.3c01892. Epub 2024 Feb 13.

Abstract

Delamanid, bedaquiline, and pretomanid have been recently added in the anti-tuberculosis (anti-TB) treatment regimens and have emerged as potential solutions for combating drug-resistant TB. These drugs have proven to be effective in treating drug-resistant TB when used in combination. However, concerns have been raised about the eventual loss of these drugs due to evolving resistance mechanisms and certain adverse effects such as prolonged QT period, gastrointestinal problems, hepatotoxicity, and renal disorders. This Perspective emphasizes the properties of these first-in-class drugs, including their mechanism of action, pharmacokinetics/pharmacodynamics profiles, clinical studies, adverse events, and underlying resistance mechanisms. A brief coverage of efforts toward the generation of best-in-class leads in each class is also provided. The ongoing clinical trials of new combinations of these drugs are discussed, thus providing a better insight into the use of these drugs while designing an effective treatment regimen for resistant TB cases.

摘要

德拉马尼、贝达喹啉和普托马尼已被新近添加到抗结核(抗 TB)治疗方案中,并已成为治疗耐药结核病的潜在解决方案。这些药物在联合使用时已被证明对治疗耐药结核病有效。然而,人们担心由于耐药机制的不断发展以及某些不良反应,如 QT 间期延长、胃肠道问题、肝毒性和肾脏疾病,这些药物最终会失效。本观点强调了这些首创类药物的特性,包括它们的作用机制、药代动力学/药效学特征、临床研究、不良反应以及潜在的耐药机制。还简要介绍了在每个类别中生成最佳类别先导物的努力。讨论了这些药物新组合的正在进行的临床试验,从而在设计耐药结核病病例的有效治疗方案时,更好地了解这些药物的使用。

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