Herrera Carolina, Shattock Robin J
Section of Infectious Diseases, Faculty of Medicine, Wright-Fleming Institute, St. Mary's Campus, Imperial College, Norfolk Place, London, W2 1PG, UK,
Curr Top Microbiol Immunol. 2014;383:1-25. doi: 10.1007/82_2013_326.
The development of prevention strategies against sexual transmission of human immunodeficiency-1 virus (HIV-1) is essential to curb the rate of new infections. New prevention options include microbicides, many of which are based on antiretroviral (ARV) drugs targeting different stages of the viral replication cycle including: viral entry and fusion; reverse transcription; integration; and viral maturation through proteolytic clevage. In this review, we discuss current and new potential candidate microbicides designed to prevent mucosal HIV acquisition. Preclinical methods, including cellular, tissular, and animal models, used to assess candidate microbicides and evaluate their prioritization for progress through the product development pipeline are reviewed in context with a rapidly evolving clinical landscape.
制定针对人类免疫缺陷病毒1型(HIV-1)性传播的预防策略对于遏制新感染率至关重要。新的预防方法包括杀微生物剂,其中许多基于抗逆转录病毒(ARV)药物,这些药物针对病毒复制周期的不同阶段,包括:病毒进入与融合;逆转录;整合;以及通过蛋白水解切割实现病毒成熟。在本综述中,我们讨论了旨在预防黏膜感染HIV的现有和新的潜在候选杀微生物剂。随着临床情况的迅速演变,我们结合其背景对用于评估候选杀微生物剂并评估其在产品开发流程中推进优先级的临床前方法(包括细胞、组织和动物模型)进行了综述。