IP Library › Granted Patent US 9,616,105
Granted Patent B2
US 9,616,105 · App. 14/752,726 · Granted Apr 11, 2017

Agent for the treatment and/or prophylaxis of an autoimmune disease and for the formation of regulatory T cells

Inventors: Daniela Paulsen (Wuppertal, DE); Nina Brunner (Essen, DE); Dorothy Bray (Buckinghamshire, GB)
Assignee: AiCuris GmbH & Co. KG
A61K38/2013A61K35/17A61K45/06
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,616,105
App. No.
14/752,726
Granted
Apr 11, 2017
Kind
B2
Abstract

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.

Claims (21)

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.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 30, 2015
From: PAULSEN, DANIELA; BRUNNER, NINA; BRAY, DOROTHY
To: AICURIS GMBH & CO. KG
Reel/Frame 035943/0695 →
Priority Claims (1)
DE 10 2008 023 820 · May 8, 2008 · national
Continuity (3)
Continuation 12941885 · Nov 8, 2010
Continuation PCTEP2009003076 · Apr 28, 2009
Related Publication 20150374788A1 · Dec 31, 2015