IP Library Granted Patent US 8,609,111
Granted Patent B2
US 8,609,111 · App. 13/490,757 · Granted Dec 17, 2013

Antibodies against clostridium difficile toxins and uses thereof

Inventors: Donna M. Ambrosino (Jamaica Plain, MA); Gregory J. Babcock (Marlborough, MA); Teresa Broering (Brookline, MA); Robert Graziano (Frenchtown, NJ); Hector Javier Hernandez (Canton, MA); Israel Lowy (Dobbs Ferry, NY); Robert Mandell (Collins, IA); Deborah Molrine (Newton, MA); William D. Thomas, Jr. (Dedham, MA); Hui-Fen Zhang (Bridgewater, NJ)
Assignees: University of Massachusetts; Medarex, L.L.C.
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Quick Facts
Patent No.
US 8,609,111
App. No.
13/490,757
Granted
Dec 17, 2013
Kind
B2
Abstract

Antibodies that specifically bind to toxins of C. difficile , antigen binding portions thereof, and methods of making and using the antibodies and antigen binding portions thereof are provided herein.

Claims (43)

1. A method of treating Clostridium difficile ( C. difficile ) disease in a subject, the method comprising administering to the subject:

(a) an isolated monoclonal antibody that binds to C. difficile toxin A, or an antigen binding portion thereof, wherein the antibody binds to the same epitope of C. difficile toxin A recognized by an antibody comprising a heavy and light chain variable region having the amino acid sequences set forth in SEQ ID NOs: 1 and 4, SEQ ID NOs: 2 and 5, or SEQ ID NOs: 3 and 6, respectively; and

(b) an isolated monoclonal antibody that binds to C. difficile toxin B, or an antigen binding portion thereof, wherein the antibody binds to the same epitope of C. difficile toxin B recognized by an antibody comprising a heavy and light chain variable region having the amino acid sequences set forth in SEQ ID NOs: 54 and 58, respectively,

wherein C. difficile disease is treated in the subject.

2. A method of treating Clostridium difficile ( C. difficile ) disease in a subject, the method comprising administering to the subject:

(a) an isolated monoclonal antibody that binds to C. difficile toxin A, or an antigen binding portion thereof, wherein the antibody is selected from the group consisting of:

(i) an antibody comprising a heavy chain variable region CDR1 comprising SEQ ID NO:7, a heavy chain variable region CDR2 comprising SEQ ID NO:8, a heavy chain variable region CDR3 comprising SEQ ID NO:9, a light chain variable region CDR1 comprising SEQ ID NO:16, a light chain variable region CDR2 comprising SEQ ID NO:17 and a light chain variable region CDR3 comprising SEQ ID NO:18;

(ii) an antibody comprising a heavy chain variable region CDR1 comprising SEQ ID NO:10, a heavy chain variable region CDR2 comprising SEQ ID NO:11, a heavy chain variable region CDR3 comprising SEQ ID NO:12, a light chain variable region CDR1 comprising SEQ ID NO:19, a light chain variable region CDR2 comprising SEQ ID NO:20 and a light chain variable region CDR3 comprising SEQ ID NO:21; and

(iii) an antibody comprising a heavy chain variable region CDR1 comprising SEQ ID NO:13, a heavy chain variable region CDR2 comprising SEQ ID NO:14, a heavy chain variable region CDR3 comprising SEQ ID NO:15, a light chain variable region CDR1 comprising SEQ ID NO:22, a light chain variable region CDR2 comprising SEQ ID NO:23 and a light chain variable region CDR3 comprising SEQ ID NO:24;

and

(b) an isolated monoclonal antibody that binds to C. difficile toxin B, or an antigen binding portion thereof, wherein the antibody comprises a heavy chain variable region CDR1 comprising SEQ ID NO:62, a heavy chain variable region CDR2 comprising SEQ ID NO:64, a heavy chain variable region CDR3 comprising SEQ ID NO:66, a light chain variable region CDR1 comprising SEQ ID NO:68, a light chain variable region CDR2 comprising SEQ ID NO:70 and a light chain variable region CDR3 comprising SEQ ID NO:72,

wherein C. difficile disease is treated in the subject.

3. The method of claim 2 , wherein the isolated monoclonal antibody that binds to C. difficile toxin A, or an antigen binding portion thereof, comprises a heavy chain variable region CDR1 comprising SEQ ID NO:7, a heavy chain variable region CDR2 comprising SEQ ID NO:8, a heavy chain variable region CDR3 comprising SEQ ID NO:9, a light chain variable region CDR1 comprising SEQ ID NO:16, a light chain variable region CDR2 comprising SEQ ID NO:17 and a light chain variable region CDR3 comprising SEQ ID NO:18.

4. The method of claim 2 , wherein the isolated monoclonal antibody that binds to C. difficile toxin A, or an antigen binding portion thereof, comprises a heavy chain variable region CDR1 comprising SEQ ID NO:10, a heavy chain variable region CDR2 comprising SEQ ID NO:11, a heavy chain variable region CDR3 comprising SEQ ID NO:12, a light chain variable region CDR1 comprising SEQ ID NO:19, a light chain variable region CDR2 comprising SEQ ID NO:20 and a light chain variable region CDR3 comprising SEQ ID NO:21.

5. The method of claim 2 , wherein the isolated monoclonal antibody that binds to C. difficile toxin A, or an antigen binding portion thereof, comprises a heavy chain variable region CDR1 comprising SEQ ID NO:13, a heavy chain variable region CDR2 comprising SEQ ID NO:14, a heavy chain variable region CDR3 comprising SEQ ID NO:15, a light chain variable region CDR1 comprising SEQ ID NO:22, a light chain variable region CDR2 comprising SEQ ID NO:23 and a light chain variable region CDR3 comprising SEQ ID NO:24.

6. The method of claim 2 , wherein the method comprises administering to the subject:

(a) an isolated monoclonal antibody that binds to C. difficile toxin A, or an antigen binding portion thereof, wherein the antibody comprises a heavy and light chain variable region having the amino acid sequences set forth in SEQ ID NOs: 1 and 4, SEQ ID NOs: 2 and 5, or SEQ ID NOs: 3 and 6, respectively; and

(b) an isolated monoclonal antibody that binds to C. difficile toxin B, or an antigen binding portion thereof, wherein the antibody comprises a heavy and light chain variable region having the amino acid sequences set forth in SEQ ID NOs: 54 and 58, respectively,

wherein C. difficile disease is treated in the subject.

7. The method of claim 6 , wherein the isolated monoclonal antibody that binds to C. difficile toxin A, or an antigen binding portion thereof, comprises heavy and light chain variable regions having the amino acid sequences set forth in SEQ ID NOs: 1 and 4, respectively.

8. The method of claim 6 , wherein the isolated monoclonal antibody that binds to C. difficile toxin A, or an antigen binding portion thereof, comprises heavy and light chain variable regions having the amino acid sequences set forth in SEQ ID NOs: 2 and 5, respectively.

9. The method of claim 6 , wherein the isolated monoclonal antibody that binds to C. difficile toxin A, or an antigen binding portion thereof, comprises heavy and light chain variable regions having the amino acid sequences set forth in SEQ ID NOs: 3 and 6, respectively.

10. The method of claim 1 , wherein the antibodies, or antigen binding portions thereof, are administered separately.

11. The method of claim 1 , wherein the antibodies, or antigen binding portions thereof, are administered together.

12. The method of claim 1 , wherein the subject is human.

13. The method of claim 1 , wherein the antibodies, or antigen binding portions thereof, are administered intravenously, intramuscularly, or subcutaneously to the subject.

14. The method of claim 1 , wherein the C. difficile disease is antibiotic-associated diarrhea, C. difficile -mediated pseudomembranous colitis (PMC), diarrhea, or relapse of C. difficile -mediated disease.

15. The method of claim 1 , wherein the antibodies, or antigen binding portions thereof, are administered in combination with an antibiotic or C. difficile vaccine.

16. The method of claim 15 , wherein the antibiotic is vancomycin or metronidazole.

17. The method of claim 2 , wherein the antibodies, or antigen binding portions thereof, are administered separately.

18. The method of claim 2 , wherein the antibodies, or antigen binding portions thereof, are administered together.

19. The method of claim 2 , wherein the subject is human.

20. The method of claim 2 , wherein the antibodies, or antigen binding portions thereof, are administered intravenously, intramuscularly, or subcutaneously to the subject.

21. The method of claim 2 , wherein the C. difficile disease is antibiotic-associated diarrhea, C. difficile -mediated pseudomembranous colitis (PMC), diarrhea, or relapse of C. difficile -mediated disease.

22. The method of claim 2 , wherein the antibodies, or antigen binding portions thereof, are administered in combination with an antibiotic or C. difficile vaccine.

23. The method of claim 22 , wherein the antibiotic is vancomycin or metronidazole.

24. The method of claim 6 , wherein the antibodies, or antigen binding portions thereof, are administered separately.

25. The method of claim 6 , wherein the antibodies, or antigen binding portions thereof, are administered together.

26. The method of claim 6 , wherein the subject is human.

27. The method of claim 6 , wherein the antibodies, or antigen binding portions thereof, are administered intravenously, intramuscularly, or subcutaneously to the subject.

28. The method of claim 6 , wherein the C. difficile disease is antibiotic-associated diarrhea, C. difficile -mediated pseudomembranous colitis (PMC), diarrhea, or relapse of C. difficile -mediated disease.

29. The method of claim 6 , wherein the antibodies, or antigen binding portions thereof, are administered in combination with an antibiotic or C. difficile vaccine.

30. The method of claim 29 , wherein the antibiotic is vancomycin or metronidazole.

Assignments (4)
MERGER Recorded Jun 3, 2015
From: MEDAREX, L.L.C.
To: E. R. SQUIBB & SONS, L.L.C.
Reel/Frame 035776/0116 →
CORRECTIVE ASSIGNMENT TO CORRECT THE RECEIVING PARTY DATA ON THE PATENT ASSIGNMENT COVER SHEET PREVIOUSLY RECORDED ON REEL 031582 FRAME 0141. ASSIGNOR(S) HEREBY CONFIRMS THE CONVEYING PARTY IS MEDAREX, INC. AND RECEIVING PARTY IS MEDAREX, L.L.C.. Recorded Nov 13, 2013
From: MEDAREX, INC.
To: MEDAREX, L.L.C.
Reel/Frame 031628/0318 →
MERGER Recorded Nov 12, 2013
From: MEDAREX, INC.
To: PAUL D. GOLIAN / MEDAREX, L.L.C.
Reel/Frame 031582/0141 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 21, 2012
From: AMBROSINO, DONNA; BABCOCK, GREGORY J.; BROERING, TERESA; GRAZIANO, ROBERT; HERNANDEZ, HECTOR JAVIER; LOWY, ISRAEL; MANDELL, ROBERT; MOLRINE, DEBORAH; THOMAS, WILLIAM D., JR; ZHANG, HUI-FEN
To: UNIVERSITY OF MASSACHUSETTS; MEDAREX, INC.
Reel/Frame 028420/0734 →
Continuity (5)
Continuation 12533501 · Jul 31, 2009
Division 11051453 · Feb 4, 2005
Provisional Application 60542357 · Feb 6, 2004
Provisional Application 60613854 · Sep 28, 2004
Related Publication 20120288508A1 · Nov 15, 2012