Source:http://linkedlifedata.com/resource/pubmed/id/16934309
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rdf:type | |
lifeskim:mentions |
umls-concept:C0005768,
umls-concept:C0017262,
umls-concept:C0024398,
umls-concept:C0039194,
umls-concept:C0040300,
umls-concept:C0083032,
umls-concept:C0085358,
umls-concept:C0205216,
umls-concept:C0237753,
umls-concept:C1171362,
umls-concept:C1332714,
umls-concept:C1332717,
umls-concept:C1413244,
umls-concept:C1515670,
umls-concept:C1706438,
umls-concept:C2698600
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pubmed:issue |
1-2
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pubmed:dateCreated |
2006-11-20
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pubmed:abstractText |
Acute HIV/SIV (human/simian immunodeficiency virus) infection results in severe CD4(+) T cell depletion in lymphoid compartments. During the chronic phase of infection, CD4(+) T cell numbers rebound in blood but remain low in the gut-associated lymphoid tissue (GALT), even when viral replication is suppressed by antiretroviral therapy (ART). Thus, strategies to repopulate lymphoid compartments may ameliorate the clinical outcome of HIV/SIV infection. Interleukin (IL)-7 is a key cytokine for the maintenance of homeostatic proliferation of T cells. In HIV/SIV infection, IL-7 expression is increased, likely to compensate for T cell loss, suggesting that supraphysiological administration of IL-7 could provide additional benefit. However, the ability of T cells to respond to IL-7 is dependent on the level of expression of the IL-7 receptor (IL-7R) in T cells in various body compartments. In here, we investigated the proportion of IL-7R(+) T cells in blood, spleen, gut, and genitourinary tract of healthy and SIV-infected macaques with various degrees of CD4(+) T cell depletion. We found that the percentage of T cells expressing IL-7R was significantly lower in both CD4(+) and CD8(+) T cell subsets in SIV-infected macaques than in healthy animals and this decrease directly correlated with the CD4(+) T cell number. Importantly, the proportion of CD4(+) and CD8(+) T cells expressing IL-7R in blood paralleled that found in tissues. IL-7R(+) T cells within the SIV-specific CD8(+) T cells varied and were lowest in most tissues of viremic macaques, likely reflecting continuous antigen stimulation of effector cells.
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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:issn |
0042-6822
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
356
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
188-97
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pubmed:meshHeading |
pubmed-meshheading:16934309-Animals,
pubmed-meshheading:16934309-CD4 Lymphocyte Count,
pubmed-meshheading:16934309-CD4-Positive T-Lymphocytes,
pubmed-meshheading:16934309-CD8-Positive T-Lymphocytes,
pubmed-meshheading:16934309-Female,
pubmed-meshheading:16934309-Humans,
pubmed-meshheading:16934309-Lymphocyte Count,
pubmed-meshheading:16934309-Macaca mulatta,
pubmed-meshheading:16934309-Organ Specificity,
pubmed-meshheading:16934309-Receptors, Interleukin-7,
pubmed-meshheading:16934309-Simian Acquired Immunodeficiency Syndrome,
pubmed-meshheading:16934309-Simian immunodeficiency virus
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pubmed:articleTitle |
Decreased number of CD4+ and CD8+ T cells that express the interleukin-7 receptor in blood and tissues of SIV-infected macaques.
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pubmed:affiliation |
Animal Models and Retroviral Vaccines Section, National Cancer Institute, NCI, 41/D804, Bethesda, MD 20892-5065, USA.
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pubmed:publicationType |
Journal Article,
Research Support, N.I.H., Intramural
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