药物诱导的血小板减少症:临床前安全性评估的机制和相关性

Padma Kumar Narayanan , Scott Henry , Nianyu Li
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引用次数: 5

摘要

血小板减少症是临床上最常见的药物引起的不良血液学毒性之一。因此,体外和体内评价药物对血小板的影响是药物开发临床前安全性评估的重要组成部分。迄今为止,许多机制已确定与药物介导的血小板减少症有关。其中,有些是跨物种保守的,而另一些则不是。因此,在临床前阶段评估药物诱导的血小板减少症,以了解对人类的可转译性,需要具体情况具体分析。本章回顾了药物介导的血小板减少的机制,重点是小分子和大分子治疗的非免疫性(直接骨髓毒性)和免疫介导的血小板减少。几个体外和体内模型以及评估药物介导的血小板减少症在临床前阶段的挑战也将被讨论。
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Drug-induced thrombocytopenia: mechanisms and relevance in preclinical safety assessment

Thrombocytopenia is one of the most commonly observed drug-induced adverse hematologic toxicities in the clinic. Therefore, in vitro and in vivo evaluations of effect of drugs on platelets are an important component in preclinical safety assessment in drug development. To date, a number of mechanisms have been identified to be associated with drug-mediated thrombocytopenia. Amongst these, some are conserved across species whereas others are not. Therefore, a case-by-case approach is needed to assess drug-induced thrombocytopenia at preclinical stages to understand translatability to humans. The present chapter reviews mechanisms in drug-mediated thrombocytopenia with a focus on nonimmune (direct myelotoxicity) as well as immune-mediated thrombocytopenia by both small and large molecule therapeutics. Several in vitro and in vivo models as well as challenges in assessing drug-mediated thrombocytopenia in preclinical stages will also be discussed.

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来源期刊
Current opinion in toxicology
Current opinion in toxicology Toxicology, Biochemistry
CiteScore
8.50
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0.00%
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审稿时长
64 days
期刊最新文献
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