Publications & Reports

Pathogenesis of macrophage tropic HIV-1.

Gorry PR, Churchill M, Crowe SM, Cunningham AL, Gabuzda D
Macfarlane Burnet Institute for Medical Research and Public Health, Melbourne, Victoria, Australia. [email protected]


Despite numerous studies on the impact of viral diversity, human immunodeficiency virus type 1 (HIV-1)-specific immune responses and host factors on disease progression, we still do not have a firm understanding of the pathogenesis of HIV-1 infection.

Rapid depletion of CD4+ T-lymphocytes has been associated with a switch in viral coreceptor usage from CCR5 to CXCR4 in approximately 40 to 50% of infected individuals.

However, the majority of infected individuals who progress to AIDS harbor only CCR5-dependent (R5) viral strains. HIV-1 disease progression is associated with an enhanced tropism of R5 viral strains for cells of the monocyte/macrophage lineage (enhanced M-tropism).

However, the underlying molecular mechanisms contributing to enhanced M-tropism by R5 HIV-1 strains, and how HIV-1 variants with enhanced M-tropism cause CD4+ T-cell depletion in vivo are unknown.

This review examines the relationship between viral coreceptor usage, M-tropism, and pathogenicity of HIV-1.

We highlight evidence supporting the hypothesis that enhanced M-tropism of R5 HIV-1 results from adaptive viral evolution, resulting in HIV-1 variants that have increased ability to utilize relatively low levels of CD4 and CCR5 expressed on macrophages.

The evidence also suggests that these late-emerging, R5 viral strains have reduced sensitivity to entry inhibitors, and increased ability to cause CD4+ T-lymphocyte loss.

These variants are likely to impact HIV-1 disease progression, particularly in patients who persistently harbor only R5 viral strains.


  • Journal: Current HIV Research
  • Published: 01/01/2005
  • Volume: 3
  • Issue: 1
  • Pagination: 53-60

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