IP Library Granted Patent US 9,334,329
Granted Patent B2
US 9,334,329 · App. 14/035,731 · Granted May 10, 2016

Antibodies recognizing a carbohydrate containing epitope on CD-43 and CEA expressed on cancer cells and methods using same

Inventors: Shih-Yao Lin (Taipei, TW); Leewen Lin (Taipei, TW); Yu-Ying Tsai (Taipei, TW)
Assignee: BioAlliance C.V.
C07K16/2896C07K16/3007C07K16/3076C07K2317/24C07K2317/56C07K2317/73
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Quick Facts
Patent No.
US 9,334,329
App. No.
14/035,731
Granted
May 10, 2016
Kind
B2
Abstract

The present invention provides antibodies (such as chimeric and humanized antibodies) specifically bind to an epitope on CD43 and CEA expressed on nonhematopoietic cancer cells. In addition, the present invention also provides use of the antibodies described herein for diagnostic and therapeutic purposes.

Claims (17)

1. A polynucleotide comprising a nucleic acid sequence encoding an antibody comprising a heavy chain and a light chain, wherein

(a) the heavy chain comprises a heavy chain variable region comprising three complementary determining regions (CDRs) from the amino acid sequence of SEQ ID NO:1 and a heavy chain constant region comprising the amino acid sequence of SEQ ID NO:9, wherein the hinge region of the heavy chain constant region comprises at least one amino acid insertion, deletion or substitution; and

(b) the light chain comprises a light chain variable region comprising three complementary determining regions from the amino acid sequence of SEQ ID NO:2 and a light chain constant region comprising the amino acid sequence of SEQ ID NO:10 or a light chain constant region comprising the amino acid sequence of SEQ ID NO:10 and further comprising at least one amino acid insertion, wherein the antibody specifically binds to a carbohydrate epitope on a CD43 or a carcinoembryonic antigen (CEA) expressed by the nonhematopoietic cancer cells.

2. A vector comprising a nucleic acid sequence encoding an antibody comprising a heavy chain and a light chain, wherein

(a) the heavy chain comprises a heavy chain variable region comprising three complementary determining regions (CDRs) from the amino acid sequence of SEQ ID NO:1 and a heavy chain constant region comprising the amino acid sequence of SEQ ID NO:9, wherein the hinge region of the heavy chain constant region comprises at least one amino acid insertion, deletion or substitution; and

(b) the light chain comprises a light chain variable region comprising three complementary determining regions from the amino acid sequence of SEQ ID NO:2 and a light chain constant region comprising the amino acid sequence of SEQ ID NO:10 or a light chain constant region comprising the amino acid sequence of SEQ ID NO:10 and further comprising at least one amino acid insertion, wherein the antibody specifically binds to a carbohydrate epitope on a CD43 or a carcinoembryonic antigen (CEA) expressed by the nonhematopoietic cancer cells.

3. A host cell comprising the vector of claim 2 .

4. The polynucleotide of claim 1 , wherein the antibody is a humanized antibody.

5. The polynucleotide of claim 1 , wherein the antibody is a chimeric antibody.

6. The polynucleotide of claim 1 , wherein

(a) the heavy chain comprises a heavy chain variable region comprising three CDR regions from the amino acid sequence of SEQ ID NO:1 and a heavy chain constant region comprising the amino acid sequence selected from the group consisting of SEQ ID NOS:11-30; and

(b) the light chain comprising a light chain variable region comprising three CDR regions from the amino acid sequence of SEQ ID NO:2 and a constant region comprising the amino acid sequence selected from the group consisting of SEQ ID NOS:10 and 31-37.

7. The polynucleotide of claim 6 , wherein the heavy chain constant region comprises the amino acid sequence of SEQ ID NO:27.

8. The polynucleotide of claim 6 , wherein the heavy chain variable region comprises the amino acid sequence of residues 20-137 of SEQ ID NO:1 and the heavy chain constant region comprises the amino acid sequence of SEQ ID NO:27, and the light chain variable region comprises the amino acid sequence of residues 20-131 of SEQ ID NO:2 and the light chain constant region comprises the amino acid sequence of SEQ ID NO:10.

9. The polynucleotide of claim 6 , wherein the heavy chain constant region comprises the amino acid sequence of SEQ ID NO:29.

10. The polynucleotide of claim 6 , wherein the heavy chain variable region comprises the amino acid sequence of residues 20-137 of SEQ ID NO:1 and the heavy chain constant region comprises the amino acid sequence of SEQ ID NO:29, and the light chain variable region comprises the amino acid sequence of residues 20-131 of SEQ ID NO:2 and the light chain constant region comprises the amino acid sequence of SEQ ID NO:34.

11. The polynucleotide of claim 6 , wherein the heavy chain variable region comprises the amino acid sequence of residues 20-137 of SEQ ID NO:1 and the heavy chain constant region comprises the amino acid sequence of SEQ ID NO:29, and the light chain variable region comprises the amino acid sequence of residues 20-131 of SEQ ID NO:2 and the light chain constant region comprises the amino acid sequence of SEQ ID NO:35.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 24, 2014
From: LIN, SHIH-YAO; LIN, LEEWEN; TSAI, YU-YING
To: ABGENOMICS CORPORATION
Reel/Frame 032511/0815 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 24, 2014
From: ABGENOMICS CORPORATION
To: BIOALLIANCE C.V.
Reel/Frame 032511/0818 →
Continuity (4)
Division 13156233 · Jun 8, 2011
Division 12338934 · Dec 18, 2008
Provisional Application 61014716 · Dec 18, 2007
Related Publication 20140105899A1 · Apr 17, 2014