Phenotypic analysis of CD8+ T lymphocytes in a cohort of HIV type 1-infected patients treated with saquinavir, ritonavir, and two nucleoside analogs for 1 year, and association with plasma HIV type 1 RNA

AIDS Res Hum Retroviruses. 1999 Jul 20;15(11):963-72. doi: 10.1089/088922299310476.

Abstract

The phenotype of circulating CD8+ T lymphocytes and its association with plasma HIV-1 RNA were analyzed in 34 HIV-1-infected subjects, who were treated with saquinavir, ritonavir, and two nucleoside analogs (HAART) for 1 year. Four-color flow cytometry was applied to measure the expression of cell surface antigens CD38, HLA-DR, CD45RA, CD28, and CD62L on CD8+ T lymphocytes. The results were compared with data on 35 HIV-1-seronegative subjects, 18 untreated asymptomatic HIV-1-seropositive individuals, and 24 HIV-1-infected subjects receiving reverse transcriptase inhibitors (RTIs). Subjects receiving HAART showed a significantly elevated number and percentage of CD38- and HLA-DR-positive and CD28-negative CD8+ T lymphocytes as well as a lower percentage of naive (CD45RA+62L+) CD8+ T lymphocytes compared with HIV-1-uninfected controls. Even subjects with undetectable plasma HIV-1 RNA showed a persistent elevation of activated CD8+ T lymphocytes. However, fewer activated CD8+ T lymphocytes were observed in subjects receiving HAART than in untreated individuals and subjects administered RTIs. In individuals receiving RTIs, CD8+ cell activation was not significantly reduced compared with untreated subjects. Of all evaluated activation markers, the percentage of CD8+ T lymphocytes expressing CD38 and the combination of CD38 and HLA-DR showed the best correlation with plasma HIV-1 RNA. The persistence of CD8+ T lymphocyte activation in subjects receiving HAART strongly suggests ongoing viral activity, even in subjects with undetectable plasma HIV-1 RNA. A complete normalization of immunologic changes of CD8+ T lymphocytes would therefore require a more potent drug regimen or a longer duration of therapy.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • ADP-ribosyl Cyclase
  • ADP-ribosyl Cyclase 1
  • Adult
  • Anti-HIV Agents / administration & dosage
  • Anti-HIV Agents / therapeutic use*
  • Antigens, CD*
  • Antigens, Differentiation / analysis
  • CD28 Antigens / analysis
  • CD4-Positive T-Lymphocytes / chemistry
  • CD8-Positive T-Lymphocytes / chemistry*
  • Cell Separation
  • Cohort Studies
  • Drug Therapy, Combination
  • Female
  • Flow Cytometry
  • HIV Infections / drug therapy*
  • HIV Infections / immunology*
  • HIV-1*
  • HLA-DR Antigens / analysis
  • Humans
  • L-Selectin / analysis
  • Leukocyte Common Antigens / analysis
  • Male
  • Membrane Glycoproteins
  • NAD+ Nucleosidase / analysis
  • Phenotype
  • Protein Tyrosine Phosphatase, Non-Receptor Type 1
  • RNA, Viral / blood*
  • Ritonavir / administration & dosage
  • Ritonavir / therapeutic use*
  • Saquinavir / administration & dosage
  • Saquinavir / therapeutic use*

Substances

  • Anti-HIV Agents
  • Antigens, CD
  • Antigens, Differentiation
  • CD28 Antigens
  • HLA-DR Antigens
  • Membrane Glycoproteins
  • RNA, Viral
  • L-Selectin
  • Leukocyte Common Antigens
  • Protein Tyrosine Phosphatase, Non-Receptor Type 1
  • ADP-ribosyl Cyclase
  • CD38 protein, human
  • NAD+ Nucleosidase
  • ADP-ribosyl Cyclase 1
  • Saquinavir
  • Ritonavir