INDUCIBLE REGULATORY T-CELL GENERATION FOR HEMATOPOIETIC TRANSPLANTS
The present invention provides methods and compositions for converting non-Tregs into Tregs. The converted Tregs are referred to as inducible Tregs (iTregs). The iTregs are useful for preventing, suppressing, blocking inhibiting an immune response. For example the iTregs are useful for preventing rejection of a transplanted tissue in a human or other animal host, or protecting against graft vs host disease. The iTregs can also be used to treat autoimmune diseases.
1 . A method for inhibiting cytotoxic T-lymphocyte (CTL) activity, the method comprising contacting a cytotoxic T-lymphocyte with an effective amount of iTregs.
2 . A method for generating an immunosuppressive effect in a mammal having an alloresponse or autoimmune response, the method comprising administering to said mammal an effective amount of iTregs.
3 . The method of claim 2 , wherein said mammal having an alloresponse or autoimmune response follows tissue transplantation, and wherein the method further comprises suppressing, blocking or inhibiting graft-vs-host disease in the mammal.
4 . The method of claim 2 , wherein said mammal is a human.
5 . A method for preventing an alloresponse or an autoimmune response in a mammal, said method comprising administering to said mammal, prior to onset of an alloresponse or autoimmune response, an effective amount of iTreg to prevent said response.
6 . The method of claim 5 , wherein said mammal is treated prior to, at the time of, or immediately after tissue transplantation, and wherein the method further comprises preventing onset of graft-vs-host disease in said mammal.
7 . The method of claim 6 , wherein said mammal is treated prior to, at the time of, or immediately after tissue transplantation, and wherein the method further comprises blocking rejection of the transplanted tissue in the mammal.
8 . The method of claim 5 , wherein said mammal is a human.
9 . A method of treating a transplant recipient to reduce in said recipient an immune response against the transplant, the method comprising administering to a transplant recipient, an effective amount of iTregs to reduce an immune response against the antigen.
10 . The method of claim 9 , further comprising administering to said recipient an immunosuppressive agent.
11 . The method of claim 9 , wherein said iTregs are administered to the recipient prior to said transplant, concurrently with said transplant, or subsequent to the transplantation of the transplant.
12 . The method of claim 1 , wherein said iTregs are generated by isolating a non-Treg from peripheral blood, wherein said non-Treg is selected from the group consisting of a CD4 + cell, a CD4 + CD25 − cell, and a CD4 + CD25 − CD45RA + cell;
contacting the non-Treg with a combination of agents capable of converting said non-Treg into an iTreg, wherein the combination of agents comprise a tryptophan catabolite, and a demethylating agent selected from the group consisting of 5-aza-2′-deoxycitidine, 5-Azacytidine, and any combination thereof;
contacting the iTreg with a mTOR inhibitor, wherein the mTOR inhibitor inhibits non-Treg growth and is selected from the group consisting of tacrolimus, rapamycin, rapamycin derivative, and any combination thereof; and
costimulating the iTreg with anti-CD3 antibody and anti-CD28 antibody, wherein said iTreg is immunosuppressive, and the iTreg is expanded.
13 . The method of claim 2 , wherein said iTregs are generated by isolating a non-Treg from peripheral blood, wherein said non-Treg is selected from the group consisting of a CD4 + cell, a CD4 + CD25 − cell, and a CD4 + CD25 − CD45RA + cell;
contacting the non-Treg with a combination of agents capable of converting said non-Treg into an iTreg, wherein the combination of agents comprise a tryptophan catabolite, and a demethylating agent selected from the group consisting of 5-aza-2′-deoxycitidine, 5-Azacytidine, and any combination thereof;
contacting the iTreg with a mTOR inhibitor, wherein the mTOR inhibitor inhibits non-Treg growth and is selected from the group consisting of tacrolimus, rapamycin, rapamycin derivative, and any combination thereof; and
costimulating the iTreg with anti-CD3 antibody and anti-CD28 antibody, wherein said iTreg is immunosuppressive, and the iTreg is expanded.
14 . The method of claim 5 , wherein said iTregs are generated by isolating a non-Treg from peripheral blood, wherein said non-Treg is selected from the group consisting of a CD4 + cell, a CD4 + CD25 − cell, and a CD4 + CD25 − CD45RA + cell;
contacting the non-Treg with a combination of agents capable of converting said non-Treg into an iTreg, wherein the combination of agents comprise a tryptophan catabolite, and a demethylating agent selected from the group consisting of 5-aza-2′-deoxycitidine, 5-Azacytidine, and any combination thereof;
contacting the iTreg with a mTOR inhibitor, wherein the mTOR inhibitor inhibits non-Treg growth and is selected from the group consisting of tacrolimus, rapamycin, rapamycin derivative, and any combination thereof; and
costimulating the iTreg with anti-CD3 antibody and anti-CD28 antibody, wherein said iTreg is immunosuppressive, and the iTreg is expanded.
15 . The method of claim 9 , wherein said iTregs are generated by isolating a non-Treg from peripheral blood, wherein said non-Treg is selected from the group consisting of a CD4 + cell, a CD4 + CD25 − cell, and a CD4 + CD25 − CD45RA + cell;
contacting the non-Treg with a combination of agents capable of converting said non-Treg into an iTreg, wherein the combination of agents comprise a tryptophan catabolite, and a demethylating agent selected from the group consisting of 5-aza-2′-deoxycitidine, 5-Azacytidine, and any combination thereof;
contacting the iTreg with a mTOR inhibitor, wherein the mTOR inhibitor inhibits non-Treg growth and is selected from the group consisting of tacrolimus, rapamycin, rapamycin derivative, and any combination thereof; and
costimulating the iTreg with anti-CD3 antibody and anti-CD28 antibody, wherein said iTreg is immunosuppressive, and the iTreg is expanded.