Significantly skewed memory CD8+ T cell subsets in HIV-1 infected infants during the first year of life

Clin Immunol. 2009 Mar;130(3):280-9. doi: 10.1016/j.clim.2008.09.006. Epub 2008 Nov 8.

Abstract

HIV-1 infection causes a severe T cell compromise; however, little is known about changes in naive, memory, effector and senescent T cell subsets during the first year of life. T cell subsets were studied over the first year of life in blood from 3 infant cohorts: untreated HIV-infected, HIV-exposed but uninfected, and HIV-unexposed. In HIV-infected infants, the frequency of CCR7(+)CD45RA(+) naive CD8(+) T cells was significantly decreased, while the frequency of CCR7(-)CD45RA(-) effector memory CD8(+) T cells was increased, compared with the control cohorts. A larger population of CD8(+) T cells in HIV-infected infants displayed a phenotype consistent with senescence. Differences in CD4(+) T cell subset frequencies were less pronounced, and no significant differences were observed between exposed and unexposed HIV-uninfected infants. We concluded that the proportion of naive, memory, effector and senescent CD8(+) T cells during the first year of life is significantly altered by HIV-1 infection.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • CD4-Positive T-Lymphocytes / cytology
  • CD4-Positive T-Lymphocytes / virology
  • CD8-Positive T-Lymphocytes / immunology*
  • CD8-Positive T-Lymphocytes / virology
  • Cell Count
  • Cell Differentiation
  • Female
  • Flow Cytometry
  • HIV Infections / immunology*
  • HIV Infections / transmission
  • HIV-1* / immunology
  • Humans
  • Immunologic Memory
  • Infant, Newborn
  • Infectious Disease Transmission, Vertical
  • Phenotype
  • T-Lymphocyte Subsets / cytology
  • T-Lymphocyte Subsets / immunology*