Suppr超能文献

特异质药物反应的机制:活性代谢物的形成、蛋白质结合与免疫系统的调节。

Mechanism of idiosyncratic drug reactions: reactive metabolite formation, protein binding and the regulation of the immune system.

作者信息

Ju C, Uetrecht J P

机构信息

Molecular and Cellular Toxicology Section, Laboratory of Molecular Immunology, NHLBI, National Institutes of Health, 9000 Rockville Pike, Bethesda, MD 20892, USA.

出版信息

Curr Drug Metab. 2002 Aug;3(4):367-77. doi: 10.2174/1389200023337333.

Abstract

Drug-induced adverse reactions, especially type B reactions, represent a major clinical problem. They also impart a significant degree of uncertainty into drug development because they are often not detected until the drug has been released onto the market. Type B reactions are also termed idiosyncratic drug reactions by many investigators due to their unpredictable nature and our lack of understanding of the mechanisms involved. It is currently believed that the majority of these reactions are immune-mediated and are caused by immunogenic conjugates formed from the reaction of a reactive metabolite of a drug with cellular proteins. It has been shown that most drugs associated with idiosyncratic reactions form reactive metabolites to some degree. Covalent binding of reactive metabolites to cellular proteins has also been shown in many cases. However, studies to reveal the role of reactive metabolites and their protein-adducts in the mechanism of drug-induced idiosyncratic reactions are lacking. This review will focus on our current understanding and speculative views on how a reactive metabolite of a drug might ultimately lead to immune-mediated toxicity.

摘要

药物引起的不良反应,尤其是B型反应,是一个主要的临床问题。它们还给药物研发带来了很大程度的不确定性,因为这些反应往往直到药物上市后才被发现。由于B型反应具有不可预测性且我们对其涉及的机制缺乏了解,许多研究者也将其称为特异质药物反应。目前认为,这些反应大多是免疫介导的,由药物的活性代谢物与细胞蛋白反应形成的免疫原性缀合物引起。已经表明,大多数与特异质反应相关的药物在某种程度上都会形成活性代谢物。在许多情况下,活性代谢物与细胞蛋白的共价结合也已得到证实。然而,缺乏揭示活性代谢物及其蛋白加合物在药物引起的特异质反应机制中作用的研究。本综述将聚焦于我们目前对药物活性代谢物最终如何导致免疫介导毒性的理解和推测性观点。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验