Adoptive transfusion of tolerant dendritic cells prolong the survival of renal allografts: a systematic review. Issue 4 (November 2013) - Xia, Meng Juan
Abstract Objective The aim of this study was to systematically review the effects of transfusing Tol‐DCs induced by different methods on renal transplantation and survival time. Method PubMed and EMbase were searched for relevant articles from inception to July 20th, 2013. Renal allograft survival time was regarded as the endpoint outcome. The effects of Tol‐DCs on renal transplantation were evaluated semi‐quantitatively. Results Sixteen articles were included. There were three sources of Tol‐DCs, including bone marrow, spleen, and thoracic duct lymph node. Rats were administrated cells intravenously and 83% of mice through the portal vein. Four subtypes of bone marrow Tol‐DCs enhanced renal allograft time: immature DCs enhanced allograft survival 4.9‐fold in rats and 2.0‐fold in mice, gene modified DCs enhanced allograft survival 4.4‐fold in rats and 2.2‐fold in mice, and drug and cytokine induced enhanced allograft survival 2.9‐fold and 2.7‐fold, respectively, in rats. Tol‐DCs from the spleen and thoracic duct lymph nodes prolonged allograft survival 2.7‐fold and 1.8‐fold, respectively, in rats. 1‐2×106 doses of Tol‐DCs extended the survival time of rats following renal transplantation. The key mechanisms by which Tol‐DCs enhance allograft and overall survival included: (i) inducing T‐cell hyporeactivity; (ii) reducing the effects of cytotoxic lymphocytes; and (iii) inducing Th2 differentiation. Conclusion Bone marrow Tol‐DCs can extend allograft survival and induce immune tolerance in fully MHC‐mismatched renal transplantation in rats and mice. The effects of imDCs and gene modified Tol‐DCs in mice are less marked. In conclusion, a single‐injection of 1‐2×106 doses of bone marrow Tol‐DCs (i.v.), in combination with an immune‐suppressor, a co‐stimulator, and accessory cells can significantly extend renal allograft survival.