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解决抗病毒核苷的选择性和毒性问题。

Addressing the selectivity and toxicity of antiviral nucleosides.

作者信息

Feng Joy Y

机构信息

2158 Gilead Sciences Inc. , Foster City, USA.

出版信息

Antivir Chem Chemother. 2018 Jan-Dec;26:2040206618758524. doi: 10.1177/2040206618758524.

Abstract

Nucleoside and nucleotide analogs have played significant roles in antiviral therapies and are valued for their impressive potency and high barrier to resistance. They have been approved for treatment of herpes simplex virus-1, HIV, HBV, HCV, and influenza, and new drugs are being developed for the treatment of RSV, Ebola, coronavirus MERS, and other emerging viruses. However, this class of compounds has also experienced a high attrition rate in clinical trials due to toxicity. In this review, we discuss the utility of different biochemical and cell-based assays and provide recommendations for assessing toxicity liability before entering animal toxicity studies.

摘要

核苷和核苷酸类似物在抗病毒治疗中发挥了重要作用,因其显著的效力和高耐药屏障而受到重视。它们已被批准用于治疗单纯疱疹病毒-1、HIV、HBV、HCV和流感,并且正在开发用于治疗呼吸道合胞病毒、埃博拉病毒、中东呼吸综合征冠状病毒和其他新兴病毒的新药。然而,由于毒性,这类化合物在临床试验中的淘汰率也很高。在本综述中,我们讨论了不同生化和基于细胞的检测方法的实用性,并为在进入动物毒性研究之前评估毒性风险提供建议。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c680/5890540/cbeabca3a1a7/10.1177_2040206618758524-fig1.jpg

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