Source:http://linkedlifedata.com/resource/pubmed/id/15339990
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
9
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pubmed:dateCreated |
2004-9-1
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pubmed:abstractText |
Tissue expression of C3 is an unexpected regulator of the alloimmune response in mouse kidney transplantation. It is unclear, however, whether a direct or an indirect action of complement on the host immune response is involved. Also unknown is which of the complement effector products, cleaved C3, cleaved C5, or C5b-9, is responsible. Proximal tubular epithelial cells (PTEC) not only constitute a major target of the alloimmune response but also produce substantial amounts of C3. This study investigated the property of mouse PTEC to stimulate alloreactive T cells in a complement-dependent manner. The proliferative and cytokine responses of primed alloreactive T cells were measured after exposure to donor-specific PTEC that had been pretreated with normal mouse serum, heat-inactivated mouse serum, or complement- deficient (C3, C5, or C6) mouse sera to differentially deposit complement components. PTEC were able to stimulate alloreactive T cells in an antigen-specific manner. Complement activation leading to the deposition of cleaved C3 on PTEC enhanced the alloreactive T cell response. This complement-mediated stimulation of the T cell response was dependent on C3 but not on C5 or C6. The primary influence of tissue-bound complement was on CD4(+) T cells. Moreover, the effect of complement on alloreactive T cells was B7 dependent, shown by inhibition studies with CTLA4-Ig. These results suggest that donor epithelium-bound C3 can upregulate the alloimmune response. It is postulated that surface-bound C3 interacts with complement receptors on alloreactive T cells or on antigen presenting cells to increase allo-immune stimulation.
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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:month |
Sep
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pubmed:issn |
1046-6673
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
15
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
2414-22
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:15339990-Animals,
pubmed-meshheading:15339990-Cells, Cultured,
pubmed-meshheading:15339990-Complement C3,
pubmed-meshheading:15339990-Epithelial Cells,
pubmed-meshheading:15339990-Kidney Tubules, Proximal,
pubmed-meshheading:15339990-Mice,
pubmed-meshheading:15339990-Mice, Inbred BALB C,
pubmed-meshheading:15339990-Mice, Inbred C3H,
pubmed-meshheading:15339990-Mice, Inbred DBA,
pubmed-meshheading:15339990-T-Lymphocytes,
pubmed-meshheading:15339990-Urothelium
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pubmed:year |
2004
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pubmed:articleTitle |
Complement activation regulates the capacity of proximal tubular epithelial cell to stimulate alloreactive T cell response.
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pubmed:affiliation |
Department of Nephrology and Transplantation, 5th Floor, Thomas Guy House, Guy's Hospital, London SE1 9RT, UK.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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