Early and persistent human immunodeficiency virus type 1 (HIV-1)-specific T helper dysfunction in blood and lymph nodes following acute HIV-1 infection

J Infect Dis. 1999 Aug;180(2):278-84. doi: 10.1086/314868.

Abstract

Without potent antiretroviral therapy, most human immunodeficiency virus type 1 (HIV-1)-infected persons experience a progressive decline in CD4+ T cells and impairment in T helper function. It is unclear how soon after infection T cell dysfunction occurs. T helper responses were examined in blood and lymphoid tissue of 39 untreated patients with acute HIV-1 infection. Within the first 3 months, lymphoproliferative responses to mitogen, recall antigens, and HIV-1 antigens were impaired. After 6-9 months, responses to phytohemagglutinin and recall antigens improved. However, HIV-1-specific lymphoproliferation remained largely undetectable throughout 2 years of infection, and results were similar upon evaluation of lymphoid cells. Rare patients with HIV-1-specific responses had significantly lower plasma HIV-1 RNA levels than did nonresponders. These results indicate that T helper dysfunction occurs early after HIV-1 acquisition and that untreated individuals rarely recover HIV-specific helper responses; these findings lend support for early therapeutic intervention to prevent the destruction and further impairment of the T helper cells.

Publication types

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

MeSH terms

  • Adult
  • Candida / immunology
  • Female
  • HIV Core Protein p24 / immunology
  • HIV Envelope Protein gp120 / immunology
  • HIV Infections / immunology*
  • HIV-1 / immunology*
  • Humans
  • Leukocytes, Mononuclear / cytology
  • Leukocytes, Mononuclear / immunology
  • Lymph Nodes / cytology
  • Lymph Nodes / immunology*
  • Lymphocyte Activation*
  • Male
  • Phytohemagglutinins / immunology
  • Recombinant Proteins / immunology
  • T-Lymphocytes, Helper-Inducer / immunology*
  • Tetanus / immunology

Substances

  • HIV Core Protein p24
  • HIV Envelope Protein gp120
  • Phytohemagglutinins
  • Recombinant Proteins