| Literature DB >> 16272276 |
Alexander Sasha Krupnick1, Andrew E Gelman, Winfried Barchet, Steve Richardson, Friederike H Kreisel, Laurence A Turka, Marco Colonna, G Alexander Patterson, Daniel Kreisel.
Abstract
Unlike graft-resident donor-derived hemopoietic APCs, which decrease in number over time after transplantation, vascular endothelial cells are lifelong residents of a vascularized allograft. Endothelial cells are potent APCs for allogeneic CD8+ T lymphocytes but are unable to induce proliferation of allogeneic CD4+ T lymphocytes. Although the reason for this differential response has been poorly understood, here we report that alloantigen presentation by vascular endothelium to CD4+ T lymphocytes activates and induces CD4+25+Foxp3+ regulatory T cells, which can inhibit proliferation of alloreactive T cells both in vitro and in vivo. This process occurs independently of B7.1 costimulation but is dependent on programmed death ligand 1 (B7-H1). This finding may have important implications for tolerance induction in transplantation.Entities:
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Year: 2005 PMID: 16272276 DOI: 10.4049/jimmunol.175.10.6265
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422