CTLA-4·FasL inhibits allogeneic responses in vivo

Abstract CTLA-4·Fas ligand (CTLA-4·FasL), a paradigmatic ‘ trans signal converter protein (TSCP)’, can attach to APC (via CTLA-4 binding to B7) and direct intercellular inhibitory signals to responding T cells (via FasL binding to Fas receptor), converting an activating APC-to-T cell signal into an inhibitory one. Our previous studies established that CTLA-4·FasL inhibits human primary mixed lymphocyte reactions (MLR) and induces alloantigen-specific hyporesponsiveness ex vivo . The present study extends this to an in vivo context. Using splenocytes from MHC-mismatched C57BL/6 and Balb/c mice, we demonstrated that his 6 CTLA-4·FasL, effectively inhibits murine MLR. Moving in vivo , we demonstrated that subcutaneously administered his 6 CTLA-4·FasL modulates the in vivo response of infused allogeneic splenocytes. his 6 CTLA-4·FasL reduces the number of cells in each cell division, and increases the percentage of dead cells in each division. These findings are consistent with an antigen-induced cell death of the alloreactive cells, and bolsters recombinant TCSP promise as a therapeutic for transplantation diseases.