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Activation and Cell Cycle Antigens in CD4+and CD8+T Cells Correlate with Plasma Human Immunodeficiency Virus (HIV‐1) RNA Level in HIV‐1 Infection
Author(s) -
Jurgen M. Orendi,
Andries C. Bloem,
Jan C.C. Borleffs,
FolkoJan Wijnholds,
Nanda Vos,
Hans S.L.M. Nottet,
Maarten R. Visser,
H. Snippe,
J. Verhoef,
Charles A. Boucher
Publication year - 1998
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/314451
Subject(s) - cd38 , cd8 , virology , t cell , biology , antigen , viral replication , human leukocyte antigen , hiv antigens , immunology , cytotoxic t cell , t lymphocyte , virus , lentivirus , viral disease , immune system , in vitro , biochemistry , genetics , stem cell , cd34
The relationship between T cell activation and human immunodeficiency virus type 1 (HIV-1) replication was studied in HIV-infected subjects, 20 with and 10 without anti-HIV treatment. Expression of Ki-67 proliferation-associated antigen was increased in CD4+ and CD8+ T cells and correlated with HLA-DR. In subjects without anti-HIV treatment, the plasma HIV-1 RNA level correlated with HLA-DR in CD4+ T cells, with Ki-67 in CD8+ T cells, and with expression of CD38 in both T cell subsets. A proportion of treated subjects had increased T cell activation despite 4 months of highly active antiretroviral treatment (HAART). In subjects receiving HAART, a high percentage of HLA-DR+ CD4+ T cells was associated with signs of opportunistic infections. This work supports the concept that, in the natural course of HIV-1 infection, HIV replication itself leads to general T cell activation and that opportunistic infections generate additional CD4+ T cell activation and HIV replication.

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