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抗病毒药物研发的前景

Perspectives on antiviral drug development.

作者信息

Wainberg Mark A

机构信息

McGill University AIDS Centre, Jewish General Hospital, Montreal, Canada.

出版信息

Antiviral Res. 2009 Jan;81(1):1-5. doi: 10.1016/j.antiviral.2008.09.003. Epub 2008 Oct 21.

Abstract

The 21st International Conference on Antiviral Research provided novel insights and approaches to drug discovery across a wide array of virologic fields. Topics ranged from the chemical synthesis of new compounds against the human immunodeficiency virus (HIV) to the long-term use of established drugs against influenza. A session on novel targets for HIV therapy focused on the importance of Apobec3G, LEDGF/p75 and other cellular factors as innovative ways to control infection. New targets for hepatitis B and C viruses were surveyed. There were also discussions as to how the development of new antiviral compounds might lead to novel mechanisms of drug resistance by HIV, herpesviruses and hepatitis viruses. These covered such issues as transmission dynamics, viral fitness, the acquisition of differential resistance patterns depending on viral subtype, and clinical outcomes. Drug efficacy, toxicity, patient adherence, treatment interruption and the importance of generic drugs in resource-poor settings were also extensively discussed. These topics will all play a pivotal role in drug development and the management of viral infections in the years to come.

摘要

第21届国际抗病毒研究会议在广泛的病毒学领域为药物研发提供了新颖的见解和方法。主题涵盖从针对人类免疫缺陷病毒(HIV)的新化合物的化学合成到抗流感现有药物的长期使用。一场关于HIV治疗新靶点的会议聚焦于载脂蛋白B mRNA编辑酶催化多肽样3G(Apobec3G)、透镜状细胞核膜蛋白75(LEDGF/p75)及其他细胞因子作为控制感染的创新方式的重要性。对乙型和丙型肝炎病毒的新靶点进行了调查。还讨论了新抗病毒化合物的研发如何可能导致HIV、疱疹病毒和肝炎病毒产生新的耐药机制。这些涵盖了传播动力学、病毒适应性、取决于病毒亚型的不同耐药模式的获得以及临床结果等问题。药物疗效、毒性、患者依从性、治疗中断以及仿制药在资源匮乏地区的重要性也得到了广泛讨论。这些主题在未来几年的药物研发和病毒感染管理中将发挥关键作用。

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