4.4 Review

Affinofile profiling: How efficiency of CD4/CCR5 usage impacts the biological and pathogenic phenotype of HIV

期刊

VIROLOGY
卷 435, 期 1, 页码 81-91

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.virol.2012.09.043

关键词

HIV-1; Env; CD4; CCR5; Entry efficiency; Pathogenesis; Entry inhibitors; Cellular tropism

类别

资金

  1. UCLA AIDS Institute
  2. UCLA CFAR (Center for AIDS Research) [AI28697]
  3. NIAID [R21 AI092218]
  4. Australian National Health and Medical Research Council (NHMRC) [543103]
  5. NHMRC [1006543, 1022066]
  6. Microbial Pathogenesis Training Grant [NIH T32-AI07323]
  7. NSF [DMS-1021818]

向作者/读者索取更多资源

HIV-1 envelope (Env) uses CD4 and a coreceptor (CCR5 and/or CXCR4) for viral entry. The efficiency of receptor/coreceptor mediated entry has important implications for HIV pathogenesis and transmission. The advent of CCR5 inhibitors in clinical use also underscores the need for quantitative and predictive tools that can guide therapeutic management. Historically, measuring the efficiency of CD4/CCR5 mediated HIV entry has relied on surrogate and relatively slow throughput assays that cannot adequately capture the full spectrum of Env phenotypes. In this review, we discuss the details of the Affinofile receptor affinity profiling system that has provided a quantitative and higher throughput method to characterize viral entry efficiency as a function of CD4 and CCR5 expression levels. We will then review how the Affinofile system has been used to reveal the distinct pathophysiological properties associated with Env entry phenotypes and discuss potential shortcomings of the current system. (C) 2012 Elsevier Inc. All rights reserved.

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