Donor antigen-primed regulatory T cells permit liver regeneration and phenotype correction in hemophilia A mouse by allogeneic bone marrow stem cells

Veena Kochat, Sumod Kanjirakkuzhiyil, Prakash Baligar, Perumal Nagarajan, Asok Mukhopadhyay

Cell replacement therapy may be considered as an alternate approach to provide therapeutic dose of plasma factor VIII (FVIII) in Hemophilia A (HA) patients. However immune rejection limits the use of allogeneic cells in this mode of therapy. Here we have examined the role of donor MHC-stimulated host CD4(+)CD25(+) regulatory T (Treg) cells in suppressing immune responses against allogeneic uncommitted (Lin(-)) bone marrow cells (BMCs) for correction of bleeding disorder in HA mice. Allogeneic donor Lin(-) BMCs were co-transplanted with allo-antigen sensitized Treg cells in HA mice having acetaminophen-induced acute liver injury. Plasma FVIII activity was determined by in vitro functional assay and correction of bleeding phenotype was assessed on the basis of capillary blood clotting time and tail clip challenge. The immunosuppression potential of the sensitized Treg cells on CD4(+) T cells was studied both in vitro and in vivo. Suppression of inflammatory reactions in liver, against the homed donor cells, by sensitized Treg cells was analysed by histopathological scoring. Allo-specificity of sensitized Treg cells and long term retention of immunosuppression were examined against a third party donor and by secondary challenge of allogeneic donor cells, respectively. The engraftment and phenotype change of donor BMCs in liver and their role in synthesis of FVIII and liver regeneration were also determined. Co-transplantation of allogeneic Lin(-) BMCs with sensitized Treg cells led to systemic immune-modulation and suppression of inflammatory reactions in liver, which allowed better engraftment of allogeneic cells in liver. Allo-antigen priming led to allo-specific immune suppression even after one year of transplantation. Donor-derived endothelial cells expressed FVIII in HA mice leading to the correction of bleeding phenotype. Donor-derived hepatocyte-like cells, which constitute the major fraction of engrafted cells supported regeneration of liver after acute injury. A highly proficient FVIII secreting core system can be created in regenerating liver by transplanting allogeneic Lin(-) BMCs in HA mouse where transplantation tolerance against donor antigens can be induced by in vitro allo-antigen primed Treg cells. This strategy can be beneficial in treatments of genetic liver disorders for achieving prophylactic levels of the missing proteins.