Source:http://linkedlifedata.com/resource/pubmed/id/18372341
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
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pubmed:dateCreated |
2008-6-2
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pubmed:abstractText |
Central memory T cells are thought to play a critical role in memory T cell homoestasis by undergoing self-renewal and by maturating into effector T cells that mediate immunity at tissue sites. Circulating T cells in S phase of the cell cycle are found at increased frequencies during HIV infection and are predominantly composed of cells with a central memory phenotype. Here, we tested the hypothesis that CD4 and CD8 S-phase T cells have different capacities to complete cell cycle and survive. S-phase T cells in peripheral blood from HIV-infected donors were identified by incubating whole blood with BrdU ex vivo. Upon in vitro cultivation, S-phase T cells were more likely to die than to complete mitotic division. Intrinsic differences were observed between CD4 and CD8 S-phase T cells during incubation. Higher frequencies of CD4+ S-phase T cell underwent apoptosis after incubation in medium alone or after TCR stimulation, and CD4+ S-phase T cells were less readily induced to proliferate after incubation with IL-2 than were CD8+ S-phase T cells. CD4+ and CD8+ S-phase T cells expressed low levels of Bcl-2, which could contribute to their heightened susceptibility to cell death. Intrinsic differences in the proliferation and survival of CD4+ and CD8+ S-phase T cells could influence the homeostatic maintenance of these T cell subsets in HIV disease.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0741-5400
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
83
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1382-7
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pubmed:meshHeading |
pubmed-meshheading:18372341-Apoptosis,
pubmed-meshheading:18372341-Cells, Cultured,
pubmed-meshheading:18372341-HIV Infections,
pubmed-meshheading:18372341-Humans,
pubmed-meshheading:18372341-Interleukin-2,
pubmed-meshheading:18372341-Lymphocyte Activation,
pubmed-meshheading:18372341-Proto-Oncogene Proteins c-bcl-2,
pubmed-meshheading:18372341-Receptors, Antigen, T-Cell,
pubmed-meshheading:18372341-S Phase,
pubmed-meshheading:18372341-T-Lymphocytes
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pubmed:year |
2008
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pubmed:articleTitle |
S-phase entry leads to cell death in circulating T cells from HIV-infected persons.
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pubmed:affiliation |
Case Western Reserve University and University Hospitals of Cleveland, Center for AIDS Research, Cleveland, OH 44106, USA. sfs2@case.edu
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Research Support, N.I.H., Extramural
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