IP Library Granted Patent US 10,196,458
Granted Patent B2
US 10,196,458 · App. 14/906,026 · Granted Feb 5, 2019

Anti-immunoglobulin E antibodies and methods of using thereof

Inventors: Ke Zhang (Los Angeles, CA); Andrew Saxon (Santa Monica, CA)
Assignees: The Regents of the University of California; Sixal, Inc.
C07K16/4291A61K2039/505C07K2317/24C07K2317/76C07K2317/77C07K2317/92
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Quick Facts
Patent No.
US 10,196,458
App. No.
14/906,026
Granted
Feb 5, 2019
Kind
B2
Abstract

The present disclosure provides antibodies that specifically bind to circulating and receptor-bound IgE and inhibit IgE-mediated cell activation. The antibodies find use in various treatment, diagnostic, and monitoring applications, which are also provided.

Claims (26)

1. A method of making a pharmaceutical composition, which comprises

generating antibodies against human IgE,

selecting an antibody or fragment thereof that binds the human IgE in high affinity IgE receptors (FcεRI) on mast cells and basophils with a low affinity of 1×10 −5 M to 1×10 −8 M Kd, and

mixing the antibody or fragment thereof with a pharmaceutically acceptable carrier.

2. The method according to claim 1 , wherein the antibody or fragment thereof comprises:

a heavy chain complementary determining region 1 (HCDR1) having the amino acid sequence of SEQ ID NO: 1;

a heavy chain complementary determining region 2 (HCDR2) having the amino acid sequence of SEQ ID NO: 2;

a heavy chain complementary determining region 3 (HCDR3) having the amino acid sequence of SEQ ID NO: 3;

a light chain complementary determining region 1 (LCDR1) having the amino acid sequence of SEQ ID NO: 4;

a light chain complementary determining region 2 (LCDR2) having the amino acid sequence of SEQ ID NO: 5; and

a light chain complementary determining region 3 (LCDR3) having the amino acid sequence of SEQ ID NO: 6.

3. The method according to claim 2 , wherein the antibody or fragment thereof comprises a heavy chain polypeptide comprising a variable region having an amino acid sequence that is 85% or more identical to the heavy chain variable region set forth in SEQ ID NO: 7.

4. The method according to claim 2 , wherein the antibody or fragment thereof comprises a light chain polypeptide comprising a variable region having an amino acid sequence that is 85% or more identical to the light chain variable region set forth in SEQ ID NO: 8.

5. The method according to claim 2 , wherein the antibody or fragment thereof comprises:

a heavy chain polypeptide comprising a variable region having an amino acid sequence that is 85% or more identical to the heavy chain variable region set forth in SEQ ID NO: 7; and

a light chain polypeptide comprising a variable region having an amino acid sequence that is 85% or more identical to the light chain variable region set forth in SEQ ID NO: 8.

6. The method according to claim 1 , wherein the antibody or fragment thereof is selected from the group consisting of: an IgG, Fv, scFv, Fab, F(ab′)2, and Fab′.

7. The method according to claim 1 , wherein the antibody or fragment thereof is a bivalent anti-IgE antibody or IgE binding fragment thereof.

8. The method according to claim 1 , wherein the antibody or fragment thereof is a monoclonal anti-IgE antibody or IgE binding fragment thereof.

9. The method according to claim 1 , wherein the antibody or fragment thereof is a humanized anti-IgE antibody or IgE binding fragment thereof.

10. The method according to claim 1 , wherein the low affinity ranges from 1×10 −5 M to 1×10 −6 M Kd.

11. The method according to claim 1 , wherein the low affinity ranges from 1×10 −6 M to 1×10 −7 M Kd.

12. The method according to claim 1 , wherein the low affinity ranges from 1×10 −7 M to 1×10 −8 M Kd.

13. The method according to claim 1 , wherein the concentration of the antibody or fragment thereof is about 1 mg/mL to about 200 mg/mL.

14. The method according to claim 1 , wherein the concentration of the antibody or fragment thereof is about 50 mg/mL to about 200 mg/mL.

15. The method according to claim 1 , wherein the concentration of the antibody or fragment thereof is about 150 mg/mL to about 200 mg/mL.

Assignments (3)
CONFIRMATORY LICENSE Recorded May 22, 2016
From: UNIVERSITY OF CALIFORNIA LOS ANGELES
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 038772/0294 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 19, 2016
From: ZHANG, KE
To: THE REGENTS OF THE UNIVERSITY OF CALIFORNIA
Reel/Frame 037520/0200 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 19, 2016
From: SAXON, ANDREW
To: SIXAL, INC.
Reel/Frame 037520/0276 →
Continuity (2)
Provisional Application 61859055 · Jul 26, 2013
Related Publication 20160168268A1 · Jun 16, 2016