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Variation in the biological properties of HIV-1 R5 envelopes: Implications of envelope structure, transmission and pathogenesis: Implications of envelope structure, transmission and pathogenesis

  • Maria José Duenas-Decamp
  • , Paul J. Peters
  • , Alexander Repik
  • , Thomas Musich
  • , Maria Paz Gonzalez-Perez
  • , Catherine Caron
  • , Richard Brown
  • , Jonathan Ball
  • , Paul R. Clapham
  • University of Massachusetts Medical School
  • University of Nottingham

Research output: Contribution to journalReview articlepeer-review

21 Citations (Scopus)

Abstract

HIV-1 R5 viruses predominantly use CCR5 as a coreceptor to infect CD4 + T cells and macrophages. While R5 viruses generally infect CD4 + T cells, research over the past few years has demonstrated that they vary extensively in their capacity to infect macrophages. Thus, R5 variants that are highly macrophage tropic have been detected in late disease and are prominent in brain tissue of subjects with neurological complications. Other R5 variants that are less sensitive to CCR5 antagonists and use CCR5 differently have also been identified in late disease. These latter variants have faster replication kinetics and may contribute to CD4 T-cell depletion. In addition, R5 viruses are highly variable in many other properties, including sensitivity to neutralizing antibodies and inhibitors that block HIV-1 entry into cells. Here, we review what is currently known about how HIV-1 R5 viruses vary in cell tropism and other properties, and discuss the implications of this variation on transmission, pathogenesis, therapy and vaccines.
Original languageEnglish
Pages (from-to)435-451
Number of pages17
JournalFuture Virology
Volume5
Issue number4
DOIs
Publication statusPublished - 1 Jul 2010
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • CCR5
  • CD4
  • CD4 T cell
  • envelope
  • HIV-1
  • macrophage
  • macrophage tropism
  • neuroAIDS
  • R5
  • receptor
  • tropism

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