Acute cytomegalovirus infection is associated with increased frequencies of activated and apoptosis-vulnerable T cells in HIV-1-infected infants

J Virol. 2012 Oct;86(20):11373-9. doi: 10.1128/JVI.00790-12. Epub 2012 Aug 8.

Abstract

Cytomegalovirus (CMV) coinfection is associated with infant HIV-1 disease progression and mortality. In a cohort of Kenyan HIV-infected infants, the frequencies of activated (CD38(+) HLA-DR(+)) and apoptosis-vulnerable (CD95(+) Bcl-2(-)) CD4(+) and CD8(+) T cells increased substantially during acute CMV infection. The frequency of activated CD4(+) T cells was strongly associated with both concurrent CMV coinfection (P = 0.001) and HIV-1 viral load (P = 0.05). The frequency of apoptosis-vulnerable cells was also associated with CMV coinfection in the CD4 (P = 0.02) and CD8 (P < 0.001) T cell subsets. Similar observations were made in HIV-exposed uninfected infants. CMV-induced increases in T cell activation and apoptosis may contribute to the rapid disease progression in coinfected infants.

Publication types

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

MeSH terms

  • ADP-ribosyl Cyclase 1 / analysis
  • Apoptosis
  • CD4-Positive T-Lymphocytes / immunology*
  • CD4-Positive T-Lymphocytes / metabolism
  • CD4-Positive T-Lymphocytes / virology
  • CD8-Positive T-Lymphocytes / immunology*
  • CD8-Positive T-Lymphocytes / metabolism
  • CD8-Positive T-Lymphocytes / virology
  • Coinfection
  • Cytomegalovirus / immunology
  • Cytomegalovirus Infections / complications*
  • Cytomegalovirus Infections / immunology*
  • Cytomegalovirus Infections / virology
  • Disease Progression
  • HIV Infections / complications*
  • HIV Infections / immunology*
  • HIV Infections / virology
  • HIV-1* / immunology
  • HLA-DR Antigens / analysis
  • Humans
  • Infant
  • Kenya
  • Lymphocyte Activation*
  • Proto-Oncogene Proteins c-bcl-2 / analysis
  • Viral Load
  • fas Receptor / biosynthesis

Substances

  • HLA-DR Antigens
  • Proto-Oncogene Proteins c-bcl-2
  • fas Receptor
  • ADP-ribosyl Cyclase 1