IP Library Granted Patent US 9,441,045
Granted Patent B2
US 9,441,045 · App. 14/398,910 · Granted Sep 13, 2016

Affinity matured anti-CCR4 humanized monoclonal antibodies and methods of use

Inventors: Wayne A. Marasco (Wellesley, MA); Jianhua Sui (Waltham, MA); Quan Zhu (Needham, MA); De-Kuan Chang (Malden, MA); Thomas S. Kupper (Belmont, MA)
Assignees: Dana-Farber Cancer Institute, Inc.; The Brigham and Women's Hospital
C07K16/2866A61K47/48546C07K16/40A61K2039/505A61K2039/53C07K2317/24C07K2317/31C07K2317/35C07K2317/56C07K2317/565C07K2317/622C07K2317/64C07K2317/72C07K2317/732C07K2317/734C07K2317/92
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Quick Facts
Patent No.
US 9,441,045
App. No.
14/398,910
Granted
Sep 13, 2016
Kind
B2
Abstract

The present invention provides affinity matured humanized monoclonal antibodies, bi-specific antibodies, antibody conjugates, and fusion proteins that bind to the chemokine receptor CCR4. This antibody is derived from mAb 1567 and recognizes the same epitope. Binding of the antibodies disclosed herein to CCR4 inhibits ligand-mediated activities and is used to treat symptoms of cancer. Moreover, the antibody is used in combination with vaccines to suppress the activity of regulatory T cells.

Claims (12)

1. An isolated humanized monoclonal antibody having:

a. a heavy chain with three CDRs comprising a CDR 1 comprising amino acid sequence GYTFASQW (SEQ ID NO:22), a CDR 2 comprising amino acid sequence INPGNVNT (SEQ ID NO:27), and a CDR 3 comprising amino sequence STWYRPLDY (SEQ ID NO:30) and a light chain with three CDRs comprising a CDR 1 comprising amino acid sequence QSILYSSNQKNY (SEQ ID NO:26), a CDR 2 comprising amino acid sequence WASTRE (SEQ ID NO:28), and a CDR 3 comprising amino acid sequence HQYISSYT (SEQ ID NO:35);

b. a heavy chain with three CDRs comprising a CDR 1 comprising amino acid sequence GYTFASSW (SEQ ID NO:23), a CDR 2 comprising amino acid sequence INPGNVNT (SEQ ID NO:27), and a CDR 3 comprising amino sequence STWYRPNDY (SEQ ID NO:31) and a light chain with three CDRs comprising a CDR 1 comprising amino acid sequence QSILYSSNQKNY (SEQ ID NO:26), a CDR 2 comprising amino acid sequence WASTRE (SEQ ID NO:28), and a CDR 3 comprising amino sequence HQYKSSYT (SEQ ID NO:36);

c. a heavy chain with three CDRs comprising a CDR 1 comprising amino acid sequence GYTFASSW (SEQ ID NO:23), a CDR 2 comprising amino acid sequence INPGNVNT (SEQ ID NO:27), and a CDR 3 comprising amino sequence TTRYRPLDY (SEQ ID NO:32) and a light chain with three CDRs comprising a CDR 1 comprising amino acid sequence QSILYSSNQKNY (SEQ ID NO:26), a CDR 2 comprising amino acid sequence WASTRE (SEQ ID NO:28), and a CDR 3 comprising amino sequence HQYRSSYT (SEQ ID NO:37);

d. a heavy chain with three CDRs comprising a CDR 1 comprising amino acid sequence GYTFASQY (SEQ ID NO:24), a CDR 2 comprising amino acid sequence INPGNVNT (SEQ ID NO:27), and a CDR 3 comprising amino acid sequence LTYYRPPDY (SEQ ID NO:33) and a light chain with three CDRs comprising a CDR 1 comprising amino acid sequence QSILYSSNQKNY (SEQ ID NO:26), a CDR 2 comprising amino acid sequence WASTRE (SEQ ID NO:28), and a CDR 3 comprising amino acid sequence HQYYSSYT (SEQ ID NO:38); or

e. a heavy chain with three CDRs comprising a CDR 1 comprising amino acid sequence GYTFASAW (SEQ ID NO:25), a CDR 2 comprising amino acid sequence INPGNVNT (SEQ ID NO:27), and a CDR 3 comprising amino acid sequence STYYRPLDY (SEQ ID NO:29) and a light chain with three CDRs comprising a CDR 1 comprising amino acid sequence QSILYSSNQKNY (SEQ ID NO:26), a CDR 2 comprising amino acid sequence WASTRE (SEQ ID NO:28), and a CDR 3 comprising amino acid sequence HQYMSSYT (SEQ ID NO:39);

wherein said antibody binds human CCR4.

2. The antibody of claim 1 , wherein said antibody is monovalent or bivalent.

3. The antibody of claim 1 , wherein said isolated humanized monoclonal antibody has a binding affinity of about 1.5 nM −1 or less.

4. A method of reversing regulatory T cell-mediated suppression of effector T cell proliferation comprising contacting a population of T cells with the antibody of claim 1 .

5. A pharmaceutical composition comprising the antibody of claim 1 in an amount effective to reverse regulatory T cell-mediated suppression of effector T cell proliferation.

6. The composition of claim 5 , wherein the antibody is monovalent or bivalent.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 15, 2016
From: KUPPER, THOMAS S.
To: BRIGHAM AND WOMEN'S HOSPITAL
Reel/Frame 037989/0001 →
CONFIRMATORY LICENSE Recorded Aug 14, 2015
From: DANA-FARBER CANCER INST
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 036355/0941 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 25, 2015
From: MARASCO, WAYNE A.; SUI, JIANHUA; ZHU, QUAN; CHANG, DE-KUAN
To: DANA-FARBER CANCER INSTITUTE, INC.
Reel/Frame 035254/0896 →
Continuity (3)
Provisional Application 61642749 · May 4, 2012
Provisional Application 61785559 · Mar 14, 2013
Related Publication 20150118153A1 · Apr 30, 2015