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
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Research Support, N.I.H., Extramural
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Research Support, Non-U.S. Gov't
MeSH terms
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ADP-ribosyl Cyclase 1 / analysis
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Apoptosis
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CD4-Positive T-Lymphocytes / immunology*
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CD4-Positive T-Lymphocytes / metabolism
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CD4-Positive T-Lymphocytes / virology
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CD8-Positive T-Lymphocytes / immunology*
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CD8-Positive T-Lymphocytes / metabolism
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CD8-Positive T-Lymphocytes / virology
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Coinfection
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Cytomegalovirus / immunology
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Cytomegalovirus Infections / complications*
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Cytomegalovirus Infections / immunology*
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Cytomegalovirus Infections / virology
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Disease Progression
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HIV Infections / complications*
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HIV Infections / immunology*
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HIV Infections / virology
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HIV-1* / immunology
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HLA-DR Antigens / analysis
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Humans
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Infant
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Kenya
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Lymphocyte Activation*
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Proto-Oncogene Proteins c-bcl-2 / analysis
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Viral Load
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fas Receptor / biosynthesis
Substances
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HLA-DR Antigens
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Proto-Oncogene Proteins c-bcl-2
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fas Receptor
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ADP-ribosyl Cyclase 1