Margolis Leonid, Shattock Robin
National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland 20895, USA.
Nat Rev Microbiol. 2006 Apr;4(4):312-7. doi: 10.1038/nrmicro1387.
Understanding the mechanisms of HIV-1 transmission is crucial for the development of effective preventive microbicides and vaccine strategies, and remains one of the main goals of HIV research. Over the past decade, many studies have focused on trying to identify the 'gatekeeping' mechanism that restricts the transmission of CXCR4-utilizing HIV-1 more efficiently than CCR5-utilizing HIV-1. However, to date, no study has explained the almost perfect negative selection of the former in vivo. Here, we propose that there is no single gatekeeper and that, instead, the selective transmission of R5 HIV-1 depends on the superimposition of multiple imperfect gatekeepers.
了解HIV-1传播机制对于开发有效的预防性杀微生物剂和疫苗策略至关重要,并且仍然是HIV研究的主要目标之一。在过去十年中,许多研究致力于试图确定“守门”机制,该机制比利用CCR5的HIV-1更有效地限制利用CXCR4的HIV-1的传播。然而,迄今为止,尚无研究解释前者在体内几乎完美的阴性选择。在此,我们提出不存在单一的守门人,相反,R5 HIV-1的选择性传播取决于多个不完美守门人的叠加。