IP Library › Granted Patent US 8,906,367
Granted Patent B2
US 8,906,367 · App. 12/522,031 · Granted Dec 9, 2014

Method of providing disease-specific binding molecules and targets

Inventors: Roger Nitsch (Zumikon, CH); Christoph Hock (Erlenbach, CH); Christoph Esslinger (Zürich, CH); Marlen Knobloch (Zürich, CH); Kathrin Tissot (Neuried, DE); Jan Grimm (Duebendorf, CH)
Assignee: University of Zurich
C07K16/18C07K16/00C07K2317/77A61K2039/505C07K2317/21
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Quick Facts
Patent No.
US 8,906,367
App. No.
12/522,031
Granted
Dec 9, 2014
Kind
B2
Abstract

Provided are novel specific binding molecules, particularly human antibodies as well as fragments, derivatives and variants thereof that recognize neoepitopes of disease-associated proteins which derive from native endogenous proteins but are prevalent in the body of a patient in a variant form and/or out of their normal physiological context. In addition, pharmaceutical compositions comprising such binding molecules, antibodies and mimics thereof and methods of screening for novel binding molecules, which may or may not be antibodies as well as targets in the treatment of neurological disorders such as Alzheimer's disease are described.

Claims (31)

1. An isolated antibody or antigen-binding fragment thereof which binds to beta amyloid and comprises a heavy chain variable region (VH) and a light chain variable region (VL),

wherein the VH comprises a first complementarity determining region (VHCDR1) with the amino acid sequence SEQ ID NO:20, a VHCDR2 with the amino acid sequence SEQ ID NO:21, and a VHCDR3 with the amino acid sequences SEQ ID NO:22, and

wherein the VL comprises a VHCDR1 with the amino acid sequence SEQ ID NO:23, a VHCDR2 with the amino acid sequence SEQ ID NO:24, and a VHCDR3 with the amino acid sequence SEQ ID NO:25,

wherein the antibody or fragment thereof further comprises a human IgG1constant region or fragment thereof.

2. The antibody or antigen-binding fragment thereof of claim 1 , which is a human antibody or fragment thereof.

3. The antibody or antigen-binding fragment thereof of claim 1 , which binds to beta-amyloid plaques, cerebrovascular amyloid, or diffuse Abeta deposits.

4. The antibody or antigen-binding fragment thereof of claim 1 , wherein the VH comprises the amino acid sequence of SEQ ID NO:39, and the VL comprises the amino acid sequence of SEQ ID NO:41.

5. A composition comprising the antibody or antigen binding fragment thereof of claim 1 .

6. The composition of claim 5 further comprising an additional agent useful for treating Alzheimer's disease, selected from the group consisting of small organic molecules, anti-Abeta antibodies, and combinations thereof.

7. A kit for the diagnosis of a disorder which is characterized by abnormal accumulation and/or deposition of beta amyloid comprising the antibody or antigen-binding fragment thereof of claim 1 or 4 .

8. An isolated antibody which binds to beta amyloid and comprises a heavy chain variable region (VH) and a light chain variable region (VL), wherein

the VH comprises a first complementarity determining region (VHCDR1) with the amino acid sequence SEQ ID NO:20, a VHCDR2 with the amino acid sequence SEQ ID NO:21, and a VHCDR3 with the amino acid sequence SEQ ID NO:22,

the VL comprises a VHCDR1 with the amino acid sequence SEQ ID NO:23, a VHCDR2 with the amino acid sequence SEQ ID NO:24, and a VHCDR3 with the amino acid sequence SEQ ID NO:25,

and the antibody further comprises a human IgG1 constant region.

9. A pharmaceutical composition, comprising:

an isolated antibody or antigen-binding fragment thereof as claimed in claim 1 or claim 8 ,

and a carrier, wherein the dosage of the antibody or antigen binding fragment thereof in the pharmaceutical composition is a least 1 mg/kg of body weight.

10. The pharmaceutical composition of claim 9 , wherein the dosage of the antibody or antigen-binding fragment thereof in the pharmaceutical composition is 30 mg/kg of body weight.

11. The pharmaceutical composition of claim 9 , wherein the dosage of the antibody or antigen-binding fragment thereof in the pharmaceutical composition is within the range of 1-10 mg/kg of body weight.

12. The pharmaceutical composition of claim 9 , wherein the antibody or antigen-binding fragment thereof is a human antibody or fragment thereof.

13. The pharmaceutical composition of claim 9 , wherein the antibody or antigen-binding fragment thereof binds to beta-amyloid plaques, cerebrovascular amyloid, or diffuse Abeta deposits.

14. The pharmaceutical composition of claim 9 , wherein the VH comprises the amino acid sequence of SEQ ID NO:39, and the VL comprises the amino acid sequence of SEQ ID NO:41.

15. The pharmaceutical composition of claim 9 , further comprising an additional agent useful for treating Alzheimer's disease, selected from the group consisting of small organic molecules, anti-Abeta antibodies, and combinations thereof.

16. A method of producing an anti-beta amyloid antibody or antigen binding fragment thereof comprising:

(a) culturing a recombinant host cell comprising a first nucleic acid encoding an antibody heavy chain or fragment thereof comprising a VH comprising a VHCDR1 with the amino acid sequence SEQ ID NO:20 a VHCDR2 with the amino acid sequence SEQ ID NO:21, and a VHCDR3 with the amino acid sequence SEQ ID NO:22 and a second nucleic acid encoding an antibody light chain or fragment thereof comprising a VL comprising a VLCDR1 with the amino acid sequence SEQ ID NO:23, a VHCDR2 with the amino acid sequence SEQ ID NO:24, and a VHCDR3 with the amino acid sequence SEQ ID NO:25; and

(b) isolating the antibody or antigen-binding fragment thereof from the culture.

17. The method of claim 16 , wherein the antibody or antigen-binding fragment thereof is a human antibody or fragment thereof.

18. The method of claim 16 , wherein the antibody or antigen-binding fragment thereof binds to beta-amyloid plaques, cerebrovascular amyloid, or diffuse Abeta deposits.

19. The method of claim 16 , wherein the VH comprises the amino acid sequence of SEQ ID NO:39, and the VL comprises the amino acid sequence of SEQ ID NO:41.

20. The method of claim 16 , wherein the first and second nucleic acids are comprised in the same expression vector.

21. The method of claim 16 , wherein the first nucleic acid is contained in a first expression vector and the second nucleic acid is contained in a second expression vector.

Assignments (2)
CORRECTIVE ASSIGNMENT TO CORRECT THE CORRECT THE SPELLING CORRECTION IN THE NAME OF THE ASSIGNEE (ZURICH TO ZURICH (U-UMLAUT) PREVIOUSLY RECORDED AT REEL: 23846 FRAME: 260. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Dec 2, 2024
From: NITSCH, ROGER; HOCK, CHRISTOPH; ESSLINGER, CHRISTOPH; KNOBLOCH, MARLEN; TISSOT, KATHRIN; GRIMM, JAN
To: UNIVERSITY OF ZÜRICH
Reel/Frame 069467/0131 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 26, 2010
From: NITSCH, ROGER; HOCK, CHRISTOPH; ESSLINGER, CHRISTOPH; KNOBLOCH, MARLEN; TISSOT, KATHRIN; GRIMM, JAN
To: UNIVERSITY OF ZURICH
Reel/Frame 023846/0260 →
Priority Claims (2)
EP 07000211 · Jan 5, 2007 · regional
EP 07020341 · Oct 17, 2007 · regional
Continuity (3)
Provisional Application 60934291 · Jun 11, 2007
Provisional Application 60878831 · Jan 5, 2007
Related Publication 20100202968A1 · Aug 12, 2010