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- W2028421750 abstract "Inflammation can activate self-reactive CD8+ T cells and induce autoimmunity. Here we show in a CD8+ T cell-mediated model of type 1 diabetes that CD4+CD25+ Treg cells prevent β cell destruction following localized inflammation in the islets of Langerhans. These Treg cells accumulate preferentially in the pancreatic lymph nodes and islets but not other lymph nodes or spleen. PLN-derived Treg cells are extremely potent; only 2 × 103 cells are needed to prevent diabetes development, and their capacity to regulate is dependent on TNF-related activation induced cytokine-receptor activator of NFκB signals. Indeed, blockade of this pathway results in decreased frequency of CD4+CD25+ Treg cells in the PLN, resulting in intra-islet differentiation of CD8+ T cells into CTLs and rapid progression to diabetes." @default.
- W2028421750 created "2016-06-24" @default.
- W2028421750 creator A5064443404 @default.
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- W2028421750 date "2002-02-01" @default.
- W2028421750 modified "2023-10-15" @default.
- W2028421750 title "Pancreatic Lymph Node-Derived CD4+CD25+ Treg Cells" @default.
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- W2028421750 doi "https://doi.org/10.1016/s1074-7613(02)00279-0" @default.
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