Interspecies Incompatibilities Limit the Immunomodulatory Effect of Human Mesenchymal Stromal Cells in the Rat

被引:22
作者
Lohan, Paul [1 ]
Treacy, Oliver [1 ,2 ]
Morcos, Maurice [1 ]
Donohoe, Ellen [1 ]
O'donoghue, Yvonne [4 ]
Ryan, Aideen E. [1 ,2 ,3 ]
Elliman, Stephen J. [4 ]
Ritter, Thomas [1 ,3 ,5 ]
Griffin, Matthew D. [1 ]
机构
[1] Regenerat Med Inst, Galway, Ireland
[2] Discipline Pharmacol & Therapeut, Dublin, Ireland
[3] Natl Univ Ireland, CURAM Ctr Res Med Devices, Sch Med, Coll Med,Nursing & Hlth Sci, Galway, Ireland
[4] Orbsen Therapeut Ltd, Galway, Ireland
[5] Natl Univ Ireland Galway, Coll Med, Nursing & Hlth Sci, Regenerat Med Inst REMEDI,Biomed Sci, Newcastle Rd, Galway, Ireland
基金
爱尔兰科学基金会;
关键词
Mesenchymal stem/stromal cell; Corneal transplant; Immunomodulation; Cytokines; Xenogeneic; Transplantation; CORNEAL ALLOGRAFT SURVIVAL; STEM-CELLS; MEDIATED IMMUNOSUPPRESSION; IMMUNE-RESPONSE; INHIBIT; TRANSPLANTATION; EXPRESSION; THERAPY; MODEL; IMMUNOGENICITY;
D O I
10.1002/stem.2840
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Mesenchymal stem/stromal cells (MSC) are an immunomodulatory cell population which are under preclinical and clinical investigation for a number of inflammatory conditions including transplantation. In this study, a well-established rat corneal transplantation model was used to test the ability of human MSC to prolong corneal allograft rejection-free survival using a pre-transplant intravenous infusion protocol previously shown to be efficacious with allogeneic rat MSC. Surprisingly, pre-transplant administration of human MSC had no effect on corneal allograft survival. In vitro, human MSC failed to produce nitric oxide and upregulate IDO and, as a consequence, could not suppress rat T-cell proliferation. Furthermore, human MSC were not activated by rat pro-inflammatory cytokines. Thus, interspecies incompatibility in cytokine signaling leading to failure of MSC licensing may explain the lack of in vivo efficacy of human MSC in a rat tissue allotransplant model. Interspecies incompatibilities should be taken into consideration when interpreting preclinical data efficacy data in the context of translation to clinical trial.
引用
收藏
页码:1210 / 1215
页数:6
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