IP Library Granted Patent US 8,668,909
Granted Patent B2
US 8,668,909 · App. 12/767,635 · Granted Mar 11, 2014

Anti MIF antibodies

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Quick Facts
Patent No.
US 8,668,909
App. No.
12/767,635
Granted
Mar 11, 2014
Kind
B2
Abstract

The present invention relates to monoclonal antibodies and antigen-binding portions thereof that specifically bind to the C-terminal or the center region of macrophage migration inhibitory factor (MIF). These anti-MIF antibodies and antigen-binding portions thereof further inhibit human MIF biological function. The invention also relates to isolated heavy and light chain immunoglobulins derived from anti-MIF antibodies and nucleic acid molecules encoding such immunoglobulins. The present invention also relates to a method of identifying anti-MIF antibodies, pharmaceutical compositions comprising these antibodies and a method of using these antibodies and compositions for the treatment of MIF-related conditions.

Claims (26)

1. A monoclonal antibody or an antigen-binding portion thereof that specifically binds to the C-terminal region, said C-terminal region spanning aa 50-68, or the center region, said center region spanning aa 86-102, of human macrophage inhibitory factor (MIF) and inhibits human MIF biological function.

2. The monoclonal antibody or antigen-binding portion according to claim 1 , wherein said antibody or antigen-binding portion possesses at least one of the following properties:

a) inhibits glucocorticoid overriding (GCO) activity;

b) inhibits proliferation of cancer cells or fibroblasts;

c) binds to active MIF;

d) does not bind to non-active MIF.

3. The monoclonal antibody or antigen-binding portion according to claim 1 , wherein said antibody or antigen-binding portion binds human MIF with a K D less than 500 nM.

4. The monoclonal antibody or antigen-binding portion according to claim 1 , wherein said antibody or said antigen-binding portion binds to active MIF.

5. The monoclonal antibody according to claim 1 , wherein said antibody is selected from the group consisting of:

antibody Bax69, defined as having a V L region comprising a nucleic acid sequence of SEQ ID NO:14 and a V H region comprising a nucleic acid sequence of SEQ ID NO:20;

antibody Bax94, defined as having a V L region comprising a nucleic acid sequence of SEQ ID NO:16 and a V H region comprising a nucleic acid sequence of SEQ ID NO:22;

antibody Bax152, defined as having a V L region comprising a nucleic acid sequence of SEQ ID NO:17 and a V H region comprising a nucleic acid sequence of SEQ ID NO:23; and

antibody BaxA10, defined as having a V L region comprising a nucleic acid sequence of SEQ ID NO:18 and a V H region comprising a nucleic acid sequence of SEQ ID NO:24.

6. The monoclonal antibody according to claim 1 , wherein said antibody is an IgG4 antibody having a single mutation, whereby a-CPSC (SEQ ID NO:25) sub-sequence in the Fc region of IgG4 is changed to -CPPC (SEQ ID NO: 26).

7. The monoclonal antibody or the antigen-binding portion according to claim 1 , for use in treating an immunological disease, wherein said immunological disease is an inflammatory disease or a hyperproliferative disorder.

8. A pharmaceutical composition, comprising the monoclonal antibody or the antigen-binding portion according to claim 1 and a pharmaceutically acceptable carrier.

9. A method for treating an immunological disease in a subject, including a human, comprising the step of administering to said subject in need thereof a therapeutically effective amount of the monoclonal antibody or the antigen-binding portion according to claim 1 , wherein said antibody or said antigen binding portion further inhibits human MIF biological function;

wherein the immunological disease is selected from a group consisting of peritonitis, crescentic glomerulonephritis, and ulcerative colitis.

10. An isolated cell line that produces the monoclonal antibody or the antigen-binding portion according to claim 1 .

11. An isolated nucleic acid molecule comprising a nucleotide sequence that encodes the heavy chain, or the light chain, of the monoclonal antibody or the antigen-binding portion according to claim 1 .

12. A vector comprising the nucleic acid molecule according to claim 11 , wherein the vector comprises an expression control sequence operably linked to said nucleic acid molecule.

13. A host cell comprising the nucleic acid molecule according to claim 11 .

14. A host cell comprising a nucleic acid molecule encoding the heavy chain and a nucleic acid molecule encoding the light chain of the monoclonal antibody or the antigen-binding portion according to claim 1 .

15. A method of producing a monoclonal antibody or an antigen-binding portion thereof, comprising culturing the host cell according to claim 14 under suitable conditions and recovering said antibody or antigen-binding portion thereof.

16. The monoclonal antibody or the antigen-binding portion according to claim 7 , wherein said inflammatory disease is selected from the group consisting of crescentic glomerulonephritis, ulcerative colitis, and peritonitis.

17. A host cell comprising the vector according to claim 12 .

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 24, 2017
From: BAXTER INTERNATIONAL INC.; BAXTER HEALTHCARE SA
To: BAXALTA INCORPORATED; BAXALTA GMBH
Reel/Frame 041735/0159 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 22, 2010
From: MUELLBERG, JUERGEN; HOET, RENE
To: DYAX CORP.
Reel/Frame 024734/0653 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 22, 2010
From: KERSCHBAUMER, RANDOLF; SCHEIFLINGER, FRIEDRICH; RIEGER, MANFRED; THIELE, MICHAEL; MUDDE, GEERT C.
To: BAXTER INTERNATIONAL INC.; BAXTER HEALTHCARE S.A.
Reel/Frame 024797/0846 →