Source:http://linkedlifedata.com/resource/pubmed/id/18510631
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Predicate | Object |
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rdf:type | |
lifeskim:mentions |
umls-concept:C0035015,
umls-concept:C0035820,
umls-concept:C0039194,
umls-concept:C0085358,
umls-concept:C0205178,
umls-concept:C0205224,
umls-concept:C0390526,
umls-concept:C0450127,
umls-concept:C1123023,
umls-concept:C1332712,
umls-concept:C1332717,
umls-concept:C1413191,
umls-concept:C1413244,
umls-concept:C1548437,
umls-concept:C1706438,
umls-concept:C1882923,
umls-concept:C2698600
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pubmed:issue |
7
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pubmed:dateCreated |
2008-7-24
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pubmed:abstractText |
A subset of naturally formed sphingosine-1-phosphate receptor 1 (S1P1)-bearing CD8(+)CD44(+)CCR7(+) memory T cells has been identified in transplant recipient BALB/c (H-2(d)) mice. The frequency of this subset of memory T cells is significantly increased in the spleen, lymph nodes and skin grafts in the recipient BALB/c mice during acute skin allograft rejections. The immune-reconstitution with CD8(+)CD44(+)CCR7(+)S1P1(+) memory T cells facilitates acute skin allograft rejection in SCID mice. Being Th1-polarized and cytotoxic, CD8(+)CD44(+)CCR7(+)S1P1(+) memory T cells proliferate and differentiate immediately into effectors upon encountering allo-antigens. A siRNA against S1P1 inhibits CD8(+)CD44(+)CCR7(+)S1P1(+) memory T cell-mediated acute skin allograft rejection in SCID mice by means of knocking-down S1P1-expression. CCL21 mutant (CCL21-DeltaCT) has been used to compete with wild-type CCL21 in the course of binding to CCR7. Combined administration of siRNA S1P1 and CCL21-DeltaCT significantly prolongs the survival of skin allograft in the recipient BALB/c mice by means of inhibiting accumulation of CD8(+)CD44(+)CCR7(+)S1P1(+) memory T cells in the spleen and the skin grafts. Our data provide direct evidence that S1P1 and CCR7 are involved in the proliferation and trafficking of CD8(+)CD44(+)CCR7(+)S1P1(+) memory T cells. S1P1 may serve as a functional marker for CD8(+)CD44(+)CCR7(+) memory T cells. Targeting CD8(+)CD44(+)CCR7(+)S1P1(+) T cells may be a useful strategy to prolong the survival of allograft transplant.
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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/Antigens, CD44,
http://linkedlifedata.com/resource/pubmed/chemical/Antigens, CD8,
http://linkedlifedata.com/resource/pubmed/chemical/Ccr7 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Cd44 protein, mouse,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, CCR7,
http://linkedlifedata.com/resource/pubmed/chemical/Receptors, Lysosphingolipid
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pubmed:status |
MEDLINE
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pubmed:month |
Jul
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pubmed:issn |
1600-6143
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pubmed:author |
pubmed-author:BaojunHH,
pubmed-author:ChangAA,
pubmed-author:ChunleiYY,
pubmed-author:FeildBB,
pubmed-author:FengCC,
pubmed-author:GuangYY,
pubmed-author:HuiYY,
pubmed-author:JinquanTT,
pubmed-author:JixinZZ,
pubmed-author:LUEE,
pubmed-author:LamyLL,
pubmed-author:LuokunXX,
pubmed-author:RuijingXX,
pubmed-author:WenjunYY,
pubmed-author:XiangJJ,
pubmed-author:YouxinJJ,
pubmed-author:YulingHH,
pubmed-author:ZhuanBB
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pubmed:issnType |
Electronic
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pubmed:volume |
8
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1401-12
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pubmed:meshHeading |
pubmed-meshheading:18510631-Animals,
pubmed-meshheading:18510631-Antigens, CD44,
pubmed-meshheading:18510631-Antigens, CD8,
pubmed-meshheading:18510631-CD8-Positive T-Lymphocytes,
pubmed-meshheading:18510631-Graft Rejection,
pubmed-meshheading:18510631-Graft Survival,
pubmed-meshheading:18510631-Mice,
pubmed-meshheading:18510631-Mice, Inbred C57BL,
pubmed-meshheading:18510631-Receptors, CCR7,
pubmed-meshheading:18510631-Receptors, Lysosphingolipid,
pubmed-meshheading:18510631-Skin Transplantation,
pubmed-meshheading:18510631-T-Lymphocyte Subsets,
pubmed-meshheading:18510631-Transplantation, Homologous
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pubmed:year |
2008
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pubmed:articleTitle |
Essential role of sphingosine-1-phosphate receptor 1-bearing CD8+CD44+CCR7+ T cells in acute skin allograft rejection.
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pubmed:affiliation |
Department of Immunology, and Laboratory of Allergy and Clinical Immunology, Institute of Allergy and Immune-Related Diseases and Center for Medical Research, Wuhan University School of Medicine, Wuhan, China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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