IP Library Granted Patent US 8,247,186
Granted Patent B2
US 8,247,186 · App. 13/324,929 · Granted Aug 21, 2012

Monoclonal antibodies and their use

Assignee: Oregon Health & Science University
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Quick Facts
Patent No.
US 8,247,186
App. No.
13/324,929
Granted
Aug 21, 2012
Kind
B2
Abstract

Isolated monoclonal antibodies are disclosed herein that specifically bind a cell surface antigen expressed on the human pancreatic endocrine cells or a subset thereof, and/or a precursor thereof. Isolated monoclonal antibodies are also disclosed herein that specifically bind a cell surface antigen expressed on human pancreatic exocrine cells or human ductal cells. Humanized forms of these antibodies, and functional fragments of these antibodies, are also disclosed. The antibodies can be conjugated to an effector molecule, or a detectable marker. These antibodies are of use to detect and/or isolate pancreatic cells or a subset thereof. Methods of treating a pancreatic tumor are also disclosed.

Claims (41)

1. An isolated monoclonal antibody comprising

a heavy chain comprising an H-CDR1, H-CDR2 and H-CDR3 of a monoclonal antibody produced by a DHIC2 4-A10 hybridoma having ATCC accession number PTA-8371; and

a light chain comprising an L-CDR-1, L-CDR2 and L-CDR3 of a monoclonal antibody produced by the DHIC2 4-A 10, hybridoma having ATCC accession number PTA-8371,

wherein the monoclonal antibody specifically binds pancreatic ductal cells.

2. The isolated monoclonal antibody of claim 1 , wherein the monoclonal antibody is produced by the DHIC2 4-A10 hybridoma having ATCC accession number PTA-8371.

3. The isolated monoclonal antibody of claim 1 , the antibody comprising a human framework region.

4. An isolated antigen-binding fragment of the isolated monoclonal antibody of claim 1 , wherein the antigen binding fragment specifically binds pancreatic ductal cells.

5. The isolated antigen-binding fragment of the monoclonal antibody of claim 4 , wherein the antigen-binding fragment is a scFV, a Fv, a Fab, a F(ab′) 2 or a scFV 2 fragment.

6. The isolated monoclonal antibody of claim 1 , or an antigen-binding fragment thereof, conjugated to an effector molecule.

7. The isolated monoclonal antibody or antigen-binding fragment of claim 6 , wherein the effector molecule is a detectable marker or a toxin.

8. The isolated monoclonal antibody or antigen-binding fragment of claim 7 , wherein the detectable marker is a fluorescent marker or a radiolabel.

9. The isolated antibody or antigen-binding fragment of claim 7 , wherein the toxin comprises ricin A, abrin, diphtheria toxin or a subunit thereof, Pseudomonas exotoxin or a portion thereof, saporin, restrictocin or gelonin.

10. An isolated nucleic acid encoding the monoclonal antibody of claim 1 , or encoding an antigen binding fragment of the monoclonal antibody.

11. The isolated nucleic acid of claim 10 , operably linked to a promoter.

12. An expression vector comprising the nucleic acid of claim 10 .

13. An isolated host cell transformed with the expression vector of claim 12 .

14. A hybridoma producing the monoclonal antibody of claim 1 .

15. A composition comprising the monoclonal antibody of claim 1 or an antigen-binding fragment thereof and physiologically acceptable carrier.

16. A method for detecting a pancreatic ductal cell, the method comprising:

contacting a cell of interest with the monoclonal antibody of claim 1 or an antigen binding fragment thereof; and

detecting binding of the monoclonal antibody or the antigen binding fragment thereof to the cell,

wherein binding of the monoclonal antibody or the antigen binding fragment thereof to the cell indicates that the cell is a pancreatic ductal cell.

17. The method of claim 16 , wherein the pancreatic ductal cell is in vitro.

18. The method of claim 16 , wherein the pancreatic ductal cell is in vivo.

19. The method of claim 17 , wherein the pancreatic ductal cell is isolated from a subject that has a pancreatic endocrine cell tumor or diabetes.

20. A method of isolating a pancreatic ductal cell, comprising:

contacting a suspension of pancreatic cells with the monoclonal antibody of claim 1 or an antigen binding fragment thereof to form an immune complex; and

isolating the immune complex, thereby isolating the pancreatic ductal cell.

21. The method of claim 20 , further comprising contacting the immune complex with a second antibody that specifically binds the monoclonal antibody of claim 1 or the antigen-binding fragment thereof.

22. The method of claim 20 , wherein the monoclonal antibody of claim 1 or the antigen-binding fragment thereof is coupled to a detectable marker.

23. The method of claim 21 , wherein the second antibody is coupled to a detectable marker.

24. The method of claim 22 , wherein the detectable marker is a fluorescent marker.

25. A method for isolating a pancreatic ductal cell, the method comprising:

contacting cells with the antibody of claim 1 ;

detecting binding of the antibody to the cells; and

isolating a cell bound to the antibody,

thereby isolating the pancreatic ductal cell.

26. The method of claim 16 , wherein the cell is from a human cadaveric islet.

27. The method of claim 16 , wherein the cell is differentiated from an embryonic stem cell, an adult stem cell or a progenitor cell.

28. The method of claim 20 , wherein the cells are from a human cadaveric islet.

29. The method of claim 20 , wherein the cells are differentiated from an embryonic stem cells, an adult stem cell or a progenitor cell.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 28, 2011
From: GROMPE, MARKUS; STREETER, PHILIP R.; DORRELL, CRAIG; ABRAHAM, STEPHANIE L.; LANXON-COOKSON, KELSEA M.
To: OREGON HEALTH & SCIENCE UNIVERSITY
Reel/Frame 027451/0945 →
CHANGE OF NAME Recorded Dec 28, 2011
From: LANXON-COOKSON, KELSEA M.
To: SHOOP, KELSEA M.
Reel/Frame 027455/0867 →
Continuity (4)
Division 13010737 · Jan 20, 2011
Division 12298761
Provisional Application 60795900 · Apr 28, 2006
Related Publication 20120121512A1 · May 17, 2012