Affinity matured anti-CCR4 humanized monoclonal antibodies and methods of use
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.
1. A pharmaceutical composition comprising an isolated humanized affinity-matured monoclonal antibody capable of binding human CCR4 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).
2. The pharmaceutical composition of claim 1 , wherein the monoclonal antibody has an equilibrium dissociation constant (KD) for CCR4 of less than or equal to about 2.5 nM.
3. The pharmaceutical composition of claim 1 , wherein the monoclonal antibody has an equilibrium dissociation constant (KD) for CCR4 of about 1.5 nM or less.
4. The pharmaceutical composition of claim 1 , wherein the monoclonal antibody is present in the composition in an amount effective to reduce primary tumor growth in a human subject to whom the composition is administered.
5. The pharmaceutical composition of claim 1 , wherein the monoclonal antibody is monovalent, bivalent, or a single chain antibody.
6. The pharmaceutical composition of claim 1 , wherein the monoclonal antibody is a bi-specific antibody that also immunospecifically binds to a second antigen.