Source:http://linkedlifedata.com/resource/pubmed/id/17612589
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rdf:type | |
lifeskim:mentions |
umls-concept:C0009847,
umls-concept:C0011065,
umls-concept:C0021853,
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umls-concept:C0037224,
umls-concept:C0039194,
umls-concept:C0040690,
umls-concept:C0042776,
umls-concept:C0085358,
umls-concept:C0332197,
umls-concept:C0332281,
umls-concept:C0502330,
umls-concept:C1140618,
umls-concept:C1332717,
umls-concept:C1413244,
umls-concept:C1706438,
umls-concept:C1880177,
umls-concept:C2698600
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pubmed:issue |
10
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pubmed:dateCreated |
2007-9-17
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pubmed:abstractText |
SIV-infected macaques exhibit distinct rates of progression to AIDS and despite significant increases in CD8+ T cells, immune cells fail to control and eradicate SIV in vivo. Here, we investigated the interplay between viral reservoir sites, CD8+ T-cell activation/death and outcome. Our data provide strong evidence that mesenteric (Mes) lymph nodes represent major reservoirs not only for SIV-infected macaques progressing more rapidly toward AIDS but also in controllers. We demonstrate that macaques progressing faster display greater expression of TGF-beta and Indoleamine 2,3 dioxygenase in particular in intestinal tissues associated with a phosphorylation of the p53 protein on serine 15 in CD8+ T cells from Mes lymph nodes. These factors may act as a negative regulator of CD8+ T-cell function by inducing a Bax/Bak/Puma-dependent death pathway of effector/memory CD8+ T cells. Greater T-cell death and viral dissemination was associated with a low level of TIA-1+ expressing cells. Finally, we provide evidence that abrogation of TGF-beta in vitro enhances T-cell proliferation and reduces CD8+ T-cell death. Our data identify a mechanism of T-cell exhaustion in intestinal lymphoid organs and define a potentially effective immunological strategy for the modulation of progression to AIDS.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Apoptosis Regulatory Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Indoleamine-Pyrrole 2,3,-Dioxygenase,
http://linkedlifedata.com/resource/pubmed/chemical/Transforming Growth Factor beta,
http://linkedlifedata.com/resource/pubmed/chemical/Tumor Suppressor Protein p53
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
1350-9047
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
14
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1747-58
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pubmed:meshHeading |
pubmed-meshheading:17612589-Animals,
pubmed-meshheading:17612589-Apoptosis,
pubmed-meshheading:17612589-Apoptosis Regulatory Proteins,
pubmed-meshheading:17612589-CD8-Positive T-Lymphocytes,
pubmed-meshheading:17612589-Cell Proliferation,
pubmed-meshheading:17612589-Disease Progression,
pubmed-meshheading:17612589-Indoleamine-Pyrrole 2,3,-Dioxygenase,
pubmed-meshheading:17612589-Intestines,
pubmed-meshheading:17612589-Lymph Nodes,
pubmed-meshheading:17612589-Macaca mulatta,
pubmed-meshheading:17612589-Simian Acquired Immunodeficiency Syndrome,
pubmed-meshheading:17612589-Simian immunodeficiency virus,
pubmed-meshheading:17612589-Transforming Growth Factor beta,
pubmed-meshheading:17612589-Tumor Suppressor Protein p53
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pubmed:year |
2007
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pubmed:articleTitle |
TGF-beta in intestinal lymphoid organs contributes to the death of armed effector CD8 T cells and is associated with the absence of virus containment in rhesus macaques infected with the simian immunodeficiency virus.
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pubmed:affiliation |
CNRS URA 1930; Unité de Physiopathologie des Infections Lentivirales, Institut Pasteur, 28 rue du Docteur Roux, 75724 Paris cedex 15, France.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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