IP Library › Granted Patent US 10,851,156
Granted Patent B2
US 10,851,156 · App. 16/688,406 · Granted Dec 1, 2020

Methods of detecting pyroglutamate amyloid beta protein (3pE Aβ) using anti-3pE Aβ antibodies

Inventors: Marc Mercken (Turnhout, BE); Bianca Van Broeck (Schilde, BE); Marc Vandermeeren (Geel, BE); Bart Hermans (Beerse, BE); Astrid Bottelbergs (Antwerp, BE)
Assignee: Janssen Pharmaceutica NV
C07K16/18A61K39/3955A61P25/28G01N33/6896A01K2267/0312A61K39/395A61K49/00A61K2039/505C07K14/4711C07K2317/24C07K2317/33C07K2317/34C07K2317/51C07K2317/515C07K2317/55C07K2317/56C07K2317/565C07K2317/567C07K2317/76C07K2317/92C12Q1/37G01N33/533G01N2333/4709G01N2333/96425G01N2800/2814G01N2800/2821
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Quick Facts
Patent No.
US 10,851,156
App. No.
16/688,406
Granted
Dec 1, 2020
Kind
B2
Abstract

The invention provides an antibody or antigen binding fragments thereof that binds to 3pE Aβ and methods of making and using the antibody or antigen binding fragment thereof, including use for formulations, administration and kits. The antibody and antigen binding fragments thereof and methods disclosed are useful for diagnosis, prognosis and treatment of Alzheimer's disease or other β-amyloid-related diseases.

Claims (37)

1. A method of detecting amyloid β protein having pyroglutamate at the third amino acid residue (3pE Aβ) in a subject, the method comprising

(i) contacting a biological sample from the subject with an antibody or antigen binding fragment thereof which binds to 3pE Aβ to form an antigen-antibody immune complex,

(ii) detecting the presence of the antigen-antibody immune complex;

wherein the antibody or antigen binding fragment thereof comprises

a) a heavy chain variable region CDR1 comprising the amino acid sequence of SEQ ID NO:3,

b) a heavy chain variable region CDR2 comprising the amino acid sequence of SEQ ID NO:4,

c) a heavy chain variable region CDR3 comprising the amino acid sequence of SEQ ID NO:5,

d) a light chain variable region CDR1 comprising the amino acid sequence of SEQ ID NO:14,

e) a light chain variable region CDR2 comprising the amino acid sequence of SEQ ID NO:15, and

f) a light chain variable region CDR3 comprising the amino acid sequence of SEQ ID NO:16; and

wherein the biological sample is a tissue sample.

2. The method of claim 1 , wherein

a) the heavy chain variable region CDR1 is the amino acid sequence of SEQ ID NO:3,

b) the heavy chain variable region CDR2 is the amino acid sequence of SEQ ID NO:4,

c) the heavy chain variable region CDR3 is the amino acid sequence of SEQ ID NO:5,

d) the light chain variable region CDR1 is the amino acid sequence of SEQ ID NO:14,

e) the light chain variable region CDR2 is the amino acid sequence of SEQ ID NO:15, and

f) the light chain variable region CDR3 is the amino acid sequence of SEQ ID NO:16.

3. The method of claim 1 , wherein the antibody or antigen binding fragment thereof comprises a) a heavy chain variable region comprising the amino acid sequence of SEQ ID NO:2; and b) a light chain variable region comprising the amino acid sequence of SEQ ID NO:13.

4. The method of claim 1 , wherein the antibody or antigen binding fragment thereof comprises

a) a heavy chain of the amino acid sequence of SEQ ID NO:1; and

b) a light chain of the amino acid sequence of SEQ ID NO:12.

5. The method of claim 1 , wherein the antibody or antigen binding fragment thereof comprises

a) a heavy chain variable region of an amino acid sequence at least 98% identical to the amino acid sequence of SEQ ID NO:2 and comprises the heavy chain variable region CDR1 comprising the amino acid sequence of SEQ ID NO:3, the heavy chain variable region CDR2 comprising the amino acid sequence of SEQ ID NO:4, and the heavy chain variable region CDR3 comprising the amino acid sequence of SEQ ID NO:5; and

b) a light chain variable region of an amino acid sequence at least 98% identical to the amino acid sequence of SEQ ID NO:13 and comprises the light chain variable region CDR1 comprising the amino acid sequence of SEQ ID NO:14, the light chain variable region CDR2 comprising the amino acid sequence of SEQ ID NO:15, and the light chain variable region CDR3 comprising the amino acid sequence of SEQ ID NO:16.

6. The method of claim 2 , wherein the antibody or antigen binding fragment thereof comprises

a) a heavy chain variable region of an amino acid sequence at least 98% identical to the amino acid sequence of SEQ ID NO:2 and comprises the heavy chain variable region CDR1 of amino acid sequence of SEQ ID NO:3, the heavy chain variable region CDR2 of the amino acid sequence of SEQ ID NO:4, and the heavy chain variable region CDR3 of the amino acid sequence of SEQ ID NO:5; and

b) a light chain variable region of an amino acid sequence that is at least 98% identical to the amino acid sequence of SEQ ID NO:13 and comprises the light chain variable region CDR1 of amino acid sequence of SEQ ID NO:14, the light chain variable region CDR2 of amino acid sequence of SEQ ID NO:15, and the light chain variable region CDR3 of amino acid sequence of SEQ ID NO:16.

7. The method of claim 1 , wherein the antibody or antigen binding fragment thereof is a humanized antibody.

8. The method of claim 2 , wherein the antibody or antigen binding fragment thereof is a humanized antibody.

9. The method of claim 7 , wherein the antibody or antigen binding domain thereof competes for binding to 3pE Aβ with an antibody comprising a heavy chain of the amino acid sequence of SEQ ID NO:1 and a light chain of the amino acid sequence of SED ID NO:12.

10. The method of claim 8 , wherein the antibody or antigen binding domain thereof competes for binding to 3pE Aβ with an antibody comprising a heavy chain of the amino acid sequence of SEQ ID NO:1 and a light chain of the amino acid sequence of SED ID NO:12.

11. The method of claim 1 , wherein the subject has Alzheimer's disease.

12. The method of claim 1 , wherein the tissue sample comprises brain tissue.

13. The method of claim 1 , wherein the antibody or antigen binding fragment is immobilized on an insoluble carrier.

14. The method of claim 1 , wherein the antibody or antigen binding fragment is labeled with a radioisotope, enzyme, luminescent, or fluorescent label.

15. The method of claim 1 , wherein the antigen-antibody immune complex is measured by an enzyme-linked immunosorbent assay, Western Blot analysis, competitive immunoassay, or sandwich immunoassay.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 12, 2020
From: MERCKEN, MARC; BROECK, BIANCA VAN; VANDEMEEREN, MARC; HERMANS, BART; BOTTELBERGS, ASTRID
To: JANSSEN PHARMACEUTICA NV
Reel/Frame 054026/0279 →
Continuity (3)
Division 15801435 · Nov 2, 2017
Provisional Application 62416788 · Nov 3, 2016
Related Publication 20200165328A1 · May 28, 2020
Cited By (3)
US 12,227,567 US 12,281,166 US 12,497,458