Agent for the treatment and/or prophylaxis of an autoimmune disease and for the formation of regulatory T cells
The present invention relates to an agent for the treatment and/or prophylaxis of an autoimmune disease, an agent for the formation of regulatory T cells (T Reg ) in an organism and various methods in which the agents according to the invention are used.
1. A method for the treatment and/or prevention of the worsening of an autoimmune disease in an organism, the method comprising:
(a) administering a mutein of human interleukin-2 (hIL-2 mutein) to the organism, wherein said hIL-2 mutein has an amino acid substitution in at least one of the positions 20, 88 or 126, numbered in accordance with the hIL-2 wild type sequence as set forth in SEQ ID NO: 1; and
(b) if necessary, repeating step (a),
wherein the autoimmune disease is type I diabetes, multiple sclerosis, or systemic lupus erythematosus, and wherein the administration induces regulatory T cells in the organism.
2. The method according to claim 1 , wherein through the substitution at position 88 an asparagine is exchanged for an amino acid which is selected from the group consisting of: arginine (hIL-2-N88R), glycine (hIL-2-N88G), or isoleucine (hIL-2-N88I).
3. The method according to claim 1 , wherein through the substitution at position 20 an aspartic acid is exchanged for an amino acid which is selected from the group consisting of: histidine (hIL-2-D20H), isoleucine (hIL-2-D20I), or tyrosine (hIL-2-D20Y).
4. The method according to claim 1 , wherein through the substitution at position 126, a glutamine is exchanged for a leucine (hIL-2-Q126L).
5. The method according to claim 1 , wherein the method further comprises administering to the organism an immunosuppressant.
6. The method according to claim 5 , wherein the immunosuppressant is selected from the group consisting of: glucocorticoid, including decortin, prednisol; azathioprine; cyclosporin A; tacrolimus; an anti-T lymphocyte globulin; an anti-CD3 antibody; muromonab; an anti-CD25 antibody; basiliximab; daclizumab; an anti-TNF-α antibody; infliximab; adalimumab; azathioprine; methotrexate; cyclosporin; sirolimus; everolimus; fingolimod; CELLCEPT® (mycophenolate mofetil); myfortic; and cyclophosphamide.
7. The method according to claim 1 , wherein the autoimmune disease is type I diabetes.
8. The method according to claim 1 , wherein the autoimmune disease is multiple sclerosis.
9. The method according to claim 1 , wherein the autoimmune disease is systemic lupus erythematosus (SLE).
10. A method for the treatment and/or prevention of the worsening of an autoimmune disease in an organism, the method comprising:
(a) administering a mutein of human interleukin-2 (hIL-2 mutein) to the organism, wherein said hIL-2 mutein has an amino acid substitution in at least one of the positions 20, 88 or 126, numbered in accordance with the hIL-2 wild type sequence as set forth in SEQ ID NO: 1; and
(b) if necessary, repeating step (a),
wherein the autoimmune disease is type I diabetes or multiple sclerosis.
11. The method according to claim 10 , wherein through the substitution at position 88 an asparagine is exchanged for an amino acid which is selected from the group consisting of: arginine (hIL-2-N88R), glycine (hIL-2-N88G), or isoleucine (hIL-2-N88I).
12. The method according to claim 10 , wherein through the substitution at position 20 an aspartic acid is exchanged for an amino acid which is selected from the group consisting of: histidine (hIL-2-D20H), isoleucine (hIL-2-D20I), or tyrosine (hIL-2-D20Y).
13. The method according to claim 10 , wherein through the substitution at position 126, a glutamine is exchanged for a leucine (hIL-2-Q126L).
14. The method according to claim 10 , wherein the method further comprises administering to the organism an immunosuppressant.
15. The method according to claim 14 , wherein the immunosuppressant is selected from the group consisting of: glucocorticoid; decortin; prednisol; azathioprine; cyclosporin A; tacrolimus; an anti-T lymphocyte globulin; an anti-CD3 antibody; muromonab; an anti-CD25 antibody; basiliximab; daclizumab; an anti-TNF-α antibody; infliximab; adalimumab; azathioprine; methotrexate; cyclosporin; sirolimus; everolimus; fingolimod; CELLCEPT® (mycophenolate mofetil); myfortic; and cyclophosphamide.