IP Library Granted Patent US 9,340,608
Granted Patent B2
US 9,340,608 · App. 13/929,671 · Granted May 17, 2016

Antibodies to endoplasmin and their use

Inventors: Soldano Ferrone (Boston, MA); Xinhui Wang (Boston, MA); Thomas P. Conrads (Reston, VA); Elvira Favoino (Bari, IT); Brian L. Hood (Reston, VA)
Assignee: University of Pittsburgh—Of the Commonwealth System of Higher Education
C07K16/18C07K16/30C07K16/3053C07K16/3092G01N33/574A61K39/00C07K2317/21C07K2317/34C07K2317/622C07K2317/73C07K2317/732C07K2317/734G01N2333/4727
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Quick Facts
Patent No.
US 9,340,608
App. No.
13/929,671
Granted
May 17, 2016
Kind
B2
Abstract

Isolated monoclonal antibodies are disclosed herein that specifically bind endoplasmin. In some embodiments these antibodies are fully human. Recombinant nucleic acids encoding these antibodies, expression vectors including these nucleic acids, and host cells transformed with these expression vectors are also disclosed herein. In several embodiments the disclosed antibodies are of use for detecting and/or treating tumors that express endoplasmin, such as melanoma, breast cancer, head and neck squamous cell carcinoma, renal cancer, lung cancer, glioma, bladder cancer, ovarian cancer or pancreatic cancer. In one example, the tumor is a melanoma.

Claims (23)

1. An isolated fusion protein comprising a human monoclonal antibody or an antigen-binding fragment thereof comprising a heavy chain variable region and a light chain variable region, wherein the heavy chain variable region comprises amino acids 26-33of SEQ ID NO: 1 (CDR1), amino acids 51-58 of SEQ ID NO: 1 (CDR2), amino acids 97-103 of SEQ ID NO: 1 (CDR3) and wherein the light chain variable region comprises amino acids 27-32 of SEQ ID NO: 2 (CDR1), amino acids 50-52 of SEQ ID NO: 2 (CDR2), amino acids 89-97 of SEQ ID NO: 2 (CDR3), wherein the human monoclonal antibody or antigen binding fragment thereof specifically binds human endoplasmin, and wherein the human monoclonal antibody or antigen binding fragment thereof is linked to an effector molecule, wherein the effector molecule is a cytokine or a chemokine.

2. The isolated fusion protein of claim 1 , wherein the antibody comprises the amino acid sequence set forth as SEQ ID NO: 1.

3. The isolated fusion protein of claim 1 , wherein the antibody comprises the amino acid sequence set forth as SEQ ID NO: 2.

4. The isolated fusion protein of claim 1 , comprising the antigen binding fragment, wherein the antigen-binding fragment is a Fab, a Fab′, a F(ab)′ 2 , a single chain Fv (scFv), or a disulfide stabilized Fv (dsFv).

5. The isolated fusion protein of claim 1 , comprising the human monoclonal antibody, wherein the antibody is an IgG.

6. The isolated fusion protein of claim 1 , wherein the antibody or antigen binding fragment thereof is labeled.

7. The isolated fusion protein of claim 1 , wherein

(a) the antibody or antigen biding fragment thereof specifically binds glycosylated endoplasm, and

(b) the human monoclonal antibody or antigen-binding fragment thereof competes for binding to the glycosylated endoplasm with a second antibody comprising a heavy chain and a light chain, wherein the heavy chain of the second antibody comprises the amino acid sequence set forth as SEQ ID NO: 1 and the light chain of the second antibody comprises the amino acid sequence set forth as SEQ ID NO: 2.

8. A composition comprising the isolated fusion protein of claim 1 , and a pharmaceutically acceptable carrier.

9. The isolated fusion protein of claim 1 , wherein the effector molecule is the cytokine, and wherein the cytokine is interferon-alpha.

10. The isolated fusion protein of claim 9 , wherein the interferon alpha is linked to the human monoclonal antibody or antigen binding fragment thereof with a peptide linker.

11. A composition comprising the isolated fusion protein of claim 9 and a pharmaceutically acceptable carrier.

12. A composition comprising the isolated fusion protein of claim 10 and a pharmaceutically acceptable carrier.

13. A method of treating a subject diagnosed with cancer that expresses endoplasmin, comprising

administering to the subject a therapeutically effective amount of the fusion protein of claim 1 ,

thereby treating the cancer that expresses endoplasmin in the subject.

14. The method of claim 13 , wherein the cancer is a melanoma, breast cancer, head and neck squamous cell carcinoma, renal cancer, lung cancer, glioma, ovarian cancer, bladder cancer or pancreatic adenocarcinoma.

15. A method of detecting cancer or confirming the diagnosis of cancer in a subject, comprising:

contacting a sample from the subject with the isolated fusion protein of claim 1 ; and

detecting binding of the isolated fusion protein to the sample,

wherein an increase in binding of the isolated fusion protein to the sample as compared to binding of the fusion protein, to a control sample detects cancer in the subject or confirms the diagnosis of cancer in the subject.

16. The method of claim 15 , wherein the cancer is melanoma, breast cancer, head and neck squamous cell carcinoma, renal cancer, lung cancer, glioma, bladder cancer, ovarian cancer or pancreatic cancer.

Assignments (2)
CONFIRMATORY LICENSE Recorded Sep 6, 2013
From: UNIVERSITY OF PITTSBURGH - OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 031171/0109 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 11, 2013
From: FERRONE, SOLDANO; WANG, XINHUI; CONRADS, THOMAS P.; FAVOINO, ELVIRA; HOOD, BRIAN
To: UNIVERSITY OF PITTSBURGH - OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION
Reel/Frame 030780/0062 →
Continuity (3)
Continuation 13161432 · Jun 15, 2011
Provisional Application 61355516 · Jun 16, 2010
Related Publication 20140010811A1 · Jan 9, 2014