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Abstract
Phosphatidylinositol-3-kinases (PI3K) γ and δ are preferentially enriched in leukocytes, and defects in these signaling pathways have been shown to impair T cell activation. The effects of PI3Kγ and PI3Kδ on alloimmunity remain underexplored. Here, we show that both PI3Kγ−/− and PI3KδD910A/D910A mice receiving heart allografts have suppression of alloreactive T effector cells and delayed acute rejection. However, PI3Kδ mutation also dampens regulatory T cells (Treg). After treatment with low dose CTLA4-Ig, PI3Kγ−/−, but not PI3ΚδD910A/D910A, recipients exhibit indefinite prolongation of heart allograft survival. PI3KδD910A/D910A Tregs have increased apoptosis and impaired survival. Selective inhibition of PI3Kγ and PI3Kδ (using PI3Kδ and dual PI3Kγδ chemical inhibitors) shows that PI3Kγ inhibition compensates for the negative effect of PI3Kδ inhibition on long-term allograft survival. These data serve as a basis for future PI3K-based immune therapies for transplantation.
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Details
1 Transplantation Research Center, Renal Division, Brigham and Women’s Hospital and Harvard Medical School, Boston, MA, USA
2 Infinity Pharmaceuticals, Cambridge, MA, USA
3 Division of Transplant Surgery and Transplant Surgery Research Laboratory, Brigham and Women’s Hospital and Harvard Medical School, Boston, MA, USA
4 Center for Transplantation Sciences, Massachusetts General Hospital/Harvard Medical School, Charlestown, MA, USA
5 The Transplant Institute, Beth Israel Deaconess Medical Center/Harvard Medical School, Boston, MA, USA