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    Contributors | September 15, 2015

    Mary Karr: IMG Memoir Tutorials with Mary Karr, Lena Dunham, and Gary Shteyngart

    Editor's note: It's been 20 years since the groundbreaking memoir The Liars' Club sent Mary Karr into the literary spotlight with its phenomenal... Continue »
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      The Art of Memoir

      Mary Karr 9780062223067


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The Subversion of Treg-Mediated Transplantation Tolerance by Toll-Like Receptor Signals.

The Subversion of Treg-Mediated Transplantation Tolerance by Toll-Like Receptor Signals. Cover


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Immune activation via Toll-like receptors (TLRs) has recently been identified as an important barrier to the induction of donor-specific transplantation tolerance, but the exact mechanisms underlying this barrier remain unclear. To better understand how TLR ligation interferes with the induction of donor-specific tolerance, we used complementary murine models of skin and cardiac transplantation in which prolonged allograft acceptance is either spontaneous or pharmacologically induced with anti-CD154 mAb and rapamycin. In each model, we found that prolonged allograft survival requires the presence of natural CD4+Foxp3+ regulatory T cells, and that TLR ligation prevents graft acceptance both by interfering with natural Treg function and by promoting the differentiation of Th1 effector T cells in vivo. We further demonstrate that TLR ligands mediate these effects in the absence of IL-6, and that Th17 cells do not participate in the abrogation of tolerance by TLR ligands. Finally, in light of our observation that rapamycin induces CD4+Foxp3+ adaptive Treg conversion from alloreactive Foxp3-effector T cells, we investigated the role of these cells in the tolerance process and conclude that natural Tregs are the dominant Foxp3+ regulatory T cell subset that establishes immunoregulation in animals treated with costimulatory blockade and rapamycin. Altogether, these data suggest that TLR signals do not prevent prolonged graft acceptance by preventing alloantigen-specific adaptive Treg differentiation. Instead, graft destruction results from the ability of TLR ligands to promote Th1 differentiation and interfere with immunoregulation established by alloreactive natural CD4+Foxp3+ Tregs.

Product Details

Proquest, Umi Dissertation Publishing
Porrett, Paige Marie
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Science and Mathematics » Biology » General

The Subversion of Treg-Mediated Transplantation Tolerance by Toll-Like Receptor Signals.
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Product details pages Proquest, Umi Dissertation Publishing - English 9781243590220 Reviews:
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