Date: Monday, June 13, 2016
Session Time: 4:30pm-6:00pm
Presentation Time: 4:30pm-4:42pm
Location: Room 310
We studied the role of phosphatidylinositol-3-kinases (PI3k) γ and δ pathway in alloimmunity. Generated Foxp3-GFP-PI3kγ and -PI3kδ knockout mice (C57BL/6 background) were used in heart transplant models and GVHD models. While PI3kγ-/- and PI3kδ-/- recipients of BALB/c hearts exhibited significant heart allograft survival prolongation compared to WT (MST: 14, 14, 7 respectively), the administration of low dose CTLA4Ig (250[mu]gon day 2) induced indefinite allograft survival of the PI3kγ-/- recipients compared to WT (MST: >100 and 41) with a marked increase in Tregs and a reduced % of CD4+ and CD8+ Teff along with significant suppression of Th1/Th17 cytokines in the spleen and draining lymph nodes (DLN). Surprisingly, the absence of PI3kδ abrogated the effect of CTLA4Ig treatment with a marked decrease in Tregs with significant increase in CD4+ and CD8+ Teff in the spleen and DLN of the PI3kδ-/- recipients along with significant upregulation of Th1/Th17 cytokines. Adoptive transfer of Foxp3-GFP-PI3kδ-/- and -PI3kγ-/- Tregs into a GVHD model showed that PI3kδ-/- Tregs went more into apoptosis compared to PI3kγ-/- and WT Tregs. We also examine the effect of pharmacologic inhibition of PI3k isoforms using IPI-1828 (PI3kδ selective inhibitor) and INK-055 (PI3kγ and δ inhibitor). BALB/c heart allografts were transplanted into C57BL/6 and PI3kγ-/- mice respectively and each recipient was treated with IPI-1828 or INK-055 with or without low dose CTLA4Ig respectively. WT and PI3kγ-/- recipients treated with IPI-1828 and PI3kγ-/- recipients treated with IPI-1828 plus low dose CTLA4Ig showed similar allograft survivals as previous model (MST: 13, 20, >100 respectively). Furthermore, the allograft survival of WT recipients treated with INK-055 plus low dose CTLA4Ig confirmed that PI3kδ abrogates the effect of CTLA4Ig. Using double knockout recipients (CD28-/-PI3kγ-/- and CD28-/-PI3kδ-/- mice), allograft histology was observed and showed less lymphocyte infiltration in CD28-/-PI3kγ-/- recipient compared with CD28-/-PI3kδ-/-. Allograft survival data also reflected the histology data of CD28-/-PI3kγ-/- and CD28-/-PI3kδ-/- (MST: >30 and 27.5). Our data shows a differential role of PI3Kγ and PI3Kδ in Tregs homeostasis and function with significant application in the future of PI3K based therapies in solid organ transplantation.
CITATION INFORMATION: Uehara M, Jamil A, Solhjou Z, McGrath M, Banouni N, Evans C, Dinitto J, Winkler D, Abdi R. The Role of PI3kγ and PI3kδ in Alloimmunity. Am J Transplant. 2016;16 (suppl 3).
To cite this abstract in AMA style:Uehara M, Jamil A, Solhjou Z, McGrath M, Banouni N, Evans C, Dinitto J, Winkler D, Abdi R. The Role of PI3kγ and PI3kδ in Alloimmunity. [abstract]. Am J Transplant. 2016; 16 (suppl 3). https://atcmeetingabstracts.com/abstract/the-role-of-pi3k-and-pi3k-in-alloimmunity/. Accessed May 28, 2020.
« Back to 2016 American Transplant Congress