IP Library Granted Patent US 8,920,808
Granted Patent B2
US 8,920,808 · App. 12/447,389 · Granted Dec 30, 2014

Cytokine-based fusion proteins for treatment of multiple sclerosis

Inventor: Mark D. Mannie (Greenville, NC)
Assignee: East Carolina University
A61K39/35C07K2319/74C07K2319/40A61K9/0019C07K14/4713A61K39/0008C07K2319/33A61K47/48269A61K47/4833C07K14/52
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Quick Facts
Patent No.
US 8,920,808
App. No.
12/447,389
Granted
Dec 30, 2014
Kind
B2
Abstract

The present invention provides fusion proteins including an autoimmune antigen, an allergen antigen or an alloantigen, and an anti-inflammatory cytokine. Compositions and methods including the fusion proteins are also provided.

Claims (16)

1. A method of treating multiple sclerosis comprising administering to a subject an effective amount of a first and at least a second fusion protein, wherein the first and the at least second fusion protein each independently comprise:

(a) an encephalitogenic determinant of an autoimmune antigen selected from the group consisting of myelin basic protein (MBP), proteolipid protein (PLP), myelin oligodendrocyte glycoprotein (MOG) and myelin-associated oligodendrocytic basic protein; and

(b) an anti-inflammatory cytokine selected from the group consisting of an interleukin or interleukin receptor antagonist,

wherein the anti-inflammatory cytokine of the first fusion protein is interleukin-2 (IL-2) and the anti-inflammatory cytokine of the at least second fusion protein is interleukin-4 (IL-4), interleukin-10 (IL-10), interleukin-13 (IL-13), interleukin-16 (IL-16), interferon-beta (IFN-β) or transforming growth factor-beta (TGF-β) and the interleukin receptor antagonist is interleukin-1RA (IL-1RA).

2. The method of claim 1 , wherein the autoimmune antigen is a myelin basic protein.

3. The method of claim 2 , wherein the encephalitogenic determinant of the myelin basic protein comprises the amino acid sequence of SEQ ID NO:2.

4. The method of claim 1 , wherein the anti-inflammatory cytokine of the at least second fusion protein is interleukin-4 (IL-4), or interleukin-16 (IL-16).

5. The method of claim 1 , wherein the anti-inflammatory cytokine of the at least second fusion protein is interleukin-16 (IL-16).

6. The method of claim 1 , wherein the anti-inflammatory cytokine of the at least second fusion protein is interferon-beta (IFN-β).

7. The method of claim 1 , wherein the anti-inflammatory cytokine of the at least second fusion protein is transforming growth factor-beta (TGF-β).

8. The method of claim 1 , wherein the autoimmune antigen is a proteolipid protein.

9. The method of claim 1 , wherein the autoimmune antigen is a myelin oligodendrocyte glycoprotein.

10. A method of treating multiple sclerosis comprising administering to a subject an effective amount of a first and at least a second fusion protein, wherein the first and the at least second fusion protein each independently comprise:

(a) an encephalitogenic determinant of an autoimmune antigen selected from the group consisting of myelin basic protein (MBP), proteolipid protein (PLP), myelin oligodendrocyte glycoprotein (MOG) and myelin-associated oligodendrocytic basic protein; and

(b) an anti-inflammatory cytokine selected from the group consisting of an interleukin or interleukin receptor antagonist,

wherein the interleukin of the first fusion protein is interleukin-16 (IL-16) and the interleukin of the at least second fusion protein is interleukin-2 (IL-2).

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 6, 2009
From: MANNIE, MARK D.
To: EAST CAROLINA UNIVERSITY
Reel/Frame 022648/0600 →
Continuity (2)
Provisional Application 60863692 · Oct 31, 2006
Related Publication 20100055070A1 · Mar 4, 2010