Association of strong virus-specific CD4 T cell responses with efficient natural control of primary HIV-1 infection

AIDS. 2004 Mar 26;18(5):749-55. doi: 10.1097/00002030-200403260-00005.

Abstract

Objective: To investigate whether there are differences in the virus-specific CD4 T cell response during primary HIV-1 infection in patients who naturally (without antiretroviral intervention) control viral replication with differing efficiencies.

Methods: CD4 T cell responses to recombinant HIV proteins (Gag p24 and p55 and Env gp160) and an inactivated HIV-1 preparation were analysed using interferon-gamma ELISPOT assays (with CD8-depleted peripheral blood mononuclear cells) and by intracellular interferon-gamma staining and fluorescent-activated cell sorting.

Results: Strong HIV-specific CD4 T cell responses were detected from the earliest time-points analysed in primary infection in patients who naturally established low persisting viral loads. By contrast, HIV-specific CD4 T cell responses were weaker (at or just below the limit of detection in our assays) at similar time-points in patients who went on to establish high persisting viral loads. Statistical analysis revealed a highly significant difference (P < 0.001) between the magnitudes of the Gag p24-specific response at the earliest time-point analysed in primary infection in the two sets of patients.

Conclusions: Strong HIV-specific CD4 T cell responses are associated with efficient natural control of primary HIV-1 infection.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Acute Disease
  • Adult
  • Biomarkers / analysis
  • CD4-Positive T-Lymphocytes / immunology*
  • Case-Control Studies
  • Cells, Cultured
  • HIV Core Protein p24 / pharmacology
  • HIV Infections / immunology*
  • HIV-1*
  • Humans
  • Interferon-gamma / analysis
  • Lymphocyte Activation
  • Male
  • Membrane Glycoproteins / pharmacology
  • Oncogene Protein p55(v-myc) / pharmacology
  • Retrospective Studies
  • Viral Load
  • Virus Replication

Substances

  • Biomarkers
  • HIV Core Protein p24
  • Membrane Glycoproteins
  • Oncogene Protein p55(v-myc)
  • elastin microfibril interface located protein
  • Interferon-gamma