利福霉素衍生物的发展和肝毒性。

Jiaojiao Zhang, Joshua Mattila, Peter Wipf, Xiaochao Ma
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引用次数: 0

摘要

利福霉素是一类对治疗结核病至关重要的抗生素。尽管利福霉素衍生物的开发已经彻底改变了结核病治疗,但它们与肝毒性有关,这限制了它们的临床应用。涉及领域:本文综述了利福霉素衍生物的发展、临床应用和肝毒性。我们强调利福霉素药物性肝损伤(DILI)的机制,并讨论提高利福霉素衍生物安全性的策略。通过检索PubMed和Scifinder检索到2025年1月前发表的相关文献。专家意见:利福霉素衍生物的肝毒性在临床实践中仍然是一个挑战。利福霉素引起肝损伤的具体机制有待进一步研究。基于机制的策略也有望防止利福霉素衍生物的毒性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Development and hepatotoxicity of rifamycin derivatives.

Introduction: Rifamycins are a class of antibiotics crucial for the treatment of tuberculosis (TB). Although the development of rifamycin derivatives has revolutionized TB therapy, they are associated with hepatotoxicity, which limits their clinical use.

Areas covered: This review summarizes the development, clinical applications, and hepatotoxicity of rifamycin derivatives. We highlight the mechanisms of rifamycin drug-induced liver injury (DILI) and discuss strategies to improve the safety profiles of rifamycin derivatives. Relevant literature was reviewed by searching PubMed and SciFinder for articles published up to January 2025.

Expert opinion: The hepatotoxicity of rifamycin derivatives remains a challenge in clinical practice. Further research is needed to clarify the detailed mechanisms of rifamycin-induced liver injury. Mechanism-based strategies are also expected to prevent the toxicity of rifamycin derivatives.

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