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pubmed-article:20620516pubmed:abstractTextRapamycin can promote the generation and homeostasis of CD4(+)Foxp3(+) regulatory T cells (Tregs) both in vitro and in vivo. The mechanisms by which rapamycin mediates this effect are poorly defined. In this study, we characterized CD4(+)Foxp3(+) Tregs in liver grafts and peripheral blood following rapamycin treatment using a syngeneic liver transplant model. Orthotopic liver transplantation was performed from Lewis (LEW) to LEW rats. In the first 2 weeks the percentage of CD4(+)Foxp3(+) Tregs was increased in the liver grafts and blood only among the rapamycin group compared with control group. Conversely, the percentage of CD4(+)Foxp3(+) Tregs in the liver graft and blood decreased in the cyclosporine group. In normal rats, rapamycin did not impact the generation of CD4(+)Foxp3(+) Tregs in the thymus. Thus, rapamycin can significantly enhance the percentages of CD4(+)Foxp3(+) Tregs in the thymus and periphery, indicating that rapamycin favors Tregs expansion and may suppress other CD4(+) T cells.lld:pubmed
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pubmed-article:20620516pubmed:authorpubmed-author:WangX HXHlld:pubmed
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pubmed-article:20620516pubmed:articleTitleRapamycin promotes the expansion of CD4(+) Foxp3(+) regulatory T cells after liver transplantation.lld:pubmed
pubmed-article:20620516pubmed:affiliationDivision of Liver Transplantation Center, Nanjing Medical University, Nanjing, China.lld:pubmed
pubmed-article:20620516pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:20620516pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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