IP Library Granted Patent US 7,740,833
Granted Patent B2
US 7,740,833 · App. 10/573,625 · Granted Jun 22, 2010

Therapeutic uses of chemokine variants

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Quick Facts
Patent No.
US 7,740,833
App. No.
10/573,625
Granted
Jun 22, 2010
Kind
B2
Abstract

Variants of homodimer-forming chemokines, such as human CCL2, having a single amino acid substitution in the dimerization interface that alters the pattern of hydrogen bonds and acting as an obligate monomer, can antagonize natural chemokines and have anti-inflammatory activity in vivo. These variants can be used as active ingredient in pharmaceutical compositions for the treatment of inflammatory, autoimmune, or infectious diseases.

Claims (18)

1. A method for treating an autoimmune or inflammatory disease comprising the administration of an effective amount of a monomeric variant to an individual having an autoimmune or inflammatory disease,

wherein Monocyte Chemoattractant Protein 1 (MCP-1) signaling is involved in the autoimmune or inflammatory disease process and said monomeric variant comprises:

a) SEQ ID NO: 2 (CCL2-P8A);

b) SEQ ID NO: 4 (CCL2*-P8A):

c) SEQ ID NO: 2 or SEQ ID NO: 4 with the substitution of a Cysteine in position 8, 14 or 17;

d) SEQ ID NO: 2 or SEQ ID NO: 4 with the substitution of an Alanine or a Glycine in position 1; or

e) SEQ ID NO: 2 or SEQ ID NO: 4 with the addition of a Cysteine at the C-terminus.

2. The method according to claim 1 , wherein said monomeric variant comprises SEQ ID NO: 2.

3. The method according to claim 1 , wherein said monomeric variant comprises SEQ ID NO: 4.

4. The method according to claim 1 , wherein said monomeric variant contains a Cysteine in position 8, 14 or 17 of SEQ ID NO: 2.

5. The method according to claim 1 , wherein said monomeric variant further comprises a constant region of a human immunoglobulin heavy chain.

6. The method according to claim 1 , wherein the disease is multiple sclerosis.

7. The method according to claim 1 , wherein said monomeric variant comprises SEQ ID NO: 2 and said autoimmune or inflammatory disease is multiple sclerosis.

8. The method according to claim 1 , wherein said monomeric variant comprises SEQ ID NO: 2 and an additional Cysteine at the C-terminus.

9. The method according to claim 1 , wherein said monomeric variant comprises SEQ ID NO: 4 and an additional Cysteine at the C-terminus.

10. The method according to claim 1 , wherein said monomeric variant contains an Alanine or a Glycine in position 1 of SEQ ID NO: 2.

11. The method according to claim 1 , wherein said monomeric variant contains an Alanine or a Glycine in position 1 of SEQ ID NO: 4.

12. The method according to claim 1 , wherein said monomeric variant contains a Cysteine in position 8, 14 or 17 of SEQ ID NO: 4.

Assignments (3)
CHANGE OF NAME Recorded Dec 3, 2009
From: LABORATOIRES SERONO SA
To: MERCK SERONO SA
Reel/Frame 023601/0156 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 11, 2007
From: APPLIED RESEARCH SYSTEMS ARS HOLDING N.V.
To: LABORATOIRES SERONO SA
Reel/Frame 019966/0026 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 5, 2007
From: PROUDFOOT, AMANDA; SHAW, JEFFREY; JOHNSON, ZOE
To: APPLIED RESEARCH SYSTEMS ARS HOLDING N.V.
Reel/Frame 018957/0557 →