Enhanced Alleviation Of Agvhd By Tgf-Beta 1-Modified Mesenchymal Stem Cells In Mice Through Shifting M Phi Into M2 Phenotype And Promoting The Differentiation Of Treg Cells

Allogeneic haematopoietic stem cell transplantation (allo-HSCT) is the only curative method in treating haematologic malignant diseases. Graft-versus-host disease (GVHD) is a common complication post-allo-HSCT, which can be life-threatening. Mesenchymal stem cells (MSCs) as an adult stem cell with immunoregulatory function have demonstrated efficacy in steroid resistant acute GVHD (aGVHD). However, the outcome of aGVHD treated with MSCs in clinical trials varied and its underlying mechanism is still unclear. TGF-beta 1 is a potent cytokine, which plays a key role in immunoregulation. In the present study, we firstly transduced the lentivirus vector containing TGF-beta 1 gene with mouse bone marrow-derived MSCs. Then, we investigated the immunosuppressive effect of TGF-beta 1 gene-modified MSCs on lymphocytes in vitro and its preventive and therapeutical effects on murine aGVHD model in vivo. Murine MSC was successfully isolated and identified. TGF-beta 1 was efficiently transduced into mouse MSCs, and high level TGF-beta 1 was detected. MSC-TGF-beta 1 shared the same morphology and immunotypic features of normal MSC. In vitro, MSC-TGF-beta 1 showed enhanced immunosuppressive function on lymphocyte proliferation. In vivo, MSC-TGF-beta 1 showed enhanced amelioration on the severity of aGVHD both in prophylactic and therapeutic murine models. Finally, the macrophages (Mos) derived from MSC-TGF-beta 1-treated mice showed a remarkably increasing of anti-inflammatory M2-like phenotype. Furthermore, the differentiation of CD4+ CD25+ Foxp3+ Treg cells was significantly increased in MSC-TGF-beta 1-treated group. Taken together, we proved that MSC-TGF-beta 1 showed enhanced alleviation of aGVHD severity in mice by skewing macrophages into a M2 like phenotype or increasing the proportion of Treg cells, which opens a new frontier in the treatment of aGVHD.