IP Library › Granted Patent US 10,730,934
Granted Patent B2
US 10,730,934 · App. 15/880,157 · Granted Aug 4, 2020

Antibodies to

Inventors: Bret Sellman (Gaithersburg, MD); Christine Tkaczyk (Gaithersburg, MD); Partha S. Chowdhury (Gaithersburg, MD); Lei Hua (Gaithersburg, MD); Peter Pavlik (Gaithersburg, MD); Rebecca Buonpane (Gaithersburg, MD); Chew-Shun Chang (Gaithersburg, MD)
Assignee: Medlmmune, LLC
C07K16/1271A61K39/40A61K45/06G01N33/56938A61K2039/505A61K2039/507C07K2317/52C07K2317/56C07K2317/565C07K2317/567C07K2317/73C07K2317/76C07K2317/92
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Quick Facts
Patent No.
US 10,730,934
App. No.
15/880,157
Granted
Aug 4, 2020
Kind
B2
Abstract

Antibodies and antigen binding fragments thereof directed against Staphylococcus aureus ( S. aureus ) surface determinant antigens and secreted toxins are disclosed. Methods of detecting, diagnosing and treating S. aureus using the antibodies and antigen binding fragments thereof are also provided.

Claims (33)

1. A composition comprising an antibody or antigen binding fragment thereof that specifically binds to an S. aureus alpha toxin (AT) and an antibody or antigen binding fragment thereof that specifically binds to an S. aureus surface determinant antigen, wherein the antibody or antigen binding fragment thereof that specifically binds AT comprises:

a. a heavy chain variable region (VH) complementarity determining region (CDR)1 comprising the amino acid sequence of SEM NO: 69;

b. a VH CDR2 comprising the amino acid sequence of SEQ ID NO: 70;

c. a VH CDR3 comprising the amino acid sequence of SEQ ID NO: 71;

d. a light chain variable region (VL) CDR1 comprising the amino acid sequence of SEQ ID NO: 1;

e. a VL CDR2 comprising the amino acid sequence of SEQ ID NO: 2; and

f. a VL CDR3 comprising the amino acid sequence of SEQ ID NO:68.

2. The composition of claim 1 , wherein the S. aureus surface determinant antigen is selected from the group consisting of SdrC, SdrD, SdrE, ClfA, ClfB, IsdA, IsdB, IsdC, IsdE, IsdH, SpA, FnbA and PNAG.

3. The composition of claim 1 , wherein the surface determinant antigen is IsdH.

4. The composition of claim 3 , wherein the isolated antibody or antigen binding fragment thereof that specifically binds IsdH is an antibody or antigen binding fragment thereof comprising a heavy chain variable region (VH) and a light chain variable region (VH), each of which comprises three complementarity determining regions (CDR1, CDR2, and CDR3), and wherein:

a. a VH CDR1 is identical to SEQ ID NO: 90;

b. a VH CDR2 is identical to SEQ ID NO: 91;

c. a VH CDR3 is identical to SEQ ID NO: 92;

d. a VL CDR1 is identical to SEQ ID NO: 93;

e. a VL CDR2 is identical to SEQ ID NO: 94; and

f. a VL CDR3 is identical to SEQ ID NO: 95.

5. The composition of claim 1 , wherein the surface determinant antigen is ClfA.

6. The composition of claim 5 , wherein the isolated antibody or antigen binding fragment thereof that specifically binds ClfA is an antibody or antigen binding fragment thereof comprising a VH and VL amino acid sequence, wherein the VH and VL amino acid sequences correspond to SEQ ID NO: 132 and SEQ ID NO: 136; or SEQ ID NO: 140 and SEQ ID NO: 144.

7. The composition of claim 3 , further comprising an isolated antibody or antigen binding fragment thereof that specifically binds to ClfA.

8. The composition of claim 1 , wherein the antibody or antigen binding fragment thereof that specifically binds AT comprises a VH comprising the amino acid sequence of SEQ ID NO:57 and a VL comprising the amino acid sequence of SEQ ID NO:58.

9. The composition of claim 1 , wherein the antibody or antigen binding fragment thereof that specifically binds AT comprises a heavy chain comprising the amino acid sequence of SEQ ID NO:130 and a light chain comprising the amino acid sequence of SEQ ID NO:131.

10. The composition of claim 2 , wherein the antibody or antigen binding fragment thereof that specifically binds AT comprises a VH comprising the amino acid sequence of SEQ ID NO:57 and a VL comprising the amino acid sequence of SEQ ID NO:58.

11. The composition of claim 2 , wherein the antibody or antigen binding fragment thereof that specifically binds AT comprises a heavy chain comprising the amino acid sequence of SEQ ID NO:130 and a light chain comprising the amino acid sequence of SEQ ID NO:131.

12. The composition of claim 3 , wherein the antibody or antigen binding fragment thereof that specifically binds AT comprises a VH comprising the amino acid sequence of SEQ ID NO:57 and a VL comprising the amino acid sequence of SEQ ID NO:58.

13. The composition of claim 3 , wherein the antibody or antigen binding fragment thereof that specifically binds AT comprises a heavy chain comprising the amino acid sequence of SEQ ID NO:130 and a light chain comprising the amino acid sequence of SEQ ID NO:131.

14. The composition of claim 4 , wherein the antibody or antigen binding fragment thereof that specifically binds AT comprises a VH comprising the amino acid sequence of SEQ ID NO:57 and a VL comprising the amino acid sequence of SEQ ID NO:58.

15. The composition of claim 4 , wherein the antibody or antigen binding fragment thereof that specifically binds AT comprises a heavy chain comprising the amino acid sequence of SEQ ID NO:130 and a light chain comprising the amino acid sequence of SEQ ID NO:131.

16. The composition of claim 5 , wherein the antibody or antigen binding fragment thereof that specifically binds AT comprises a VH comprising the amino acid sequence of SEQ ID NO:57 and a VL comprising the amino acid sequence of SEQ ID NO:58.

17. The composition of claim 5 , wherein the antibody or antigen binding fragment thereof that specifically binds AT comprises a heavy chain comprising the amino acid sequence of SEQ ID NO:130 and a light chain comprising the amino acid sequence of SEQ ID NO:131.

18. The composition of claim 6 , wherein the antibody or antigen binding fragment thereof that specifically binds AT comprises a VH comprising the amino acid sequence of SEQ ID NO:57 and a VL comprising the amino acid sequence of SEQ ID NO:58.

19. The composition of claim 6 , wherein the antibody or antigen binding fragment thereof that specifically binds AT comprises a heavy chain comprising the amino acid sequence of SEQ ID NO:130 and a light chain comprising the amino acid sequence of SEQ ID NO:131.

20. The composition of claim 7 , wherein the antibody or antigen binding fragment thereof that specifically binds AT comprises a VH comprising the amino acid sequence of SEQ ID NO:57 and a VL comprising the amino acid sequence of SEQ ID NO:58.

21. The composition of claim 7 , wherein the antibody or antigen binding fragment thereof that specifically binds AT comprises a heavy chain comprising the amino acid sequence of SEQ ID NO:130 and a light chain comprising the amino acid sequence of SEQ ID NO:131.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 20, 2018
From: SELLMAN, BRET; TKAZCYK, CHRISTINE; CHOWDHURY, PARTHA S; HUA, LEI; PAVLIK, PETER; CHANG, CHEW-SHUN; BUONPANE, REBECCA
To: MEDIMMUNE LLC
Reel/Frame 044978/0243 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 20, 2018
From: SELLMAN, BRET; TKACZYK, CHRISTINE; CHOWDHURY, PARTHA S; HUA, LEI; PAVLIK, PETER; CHANG, CHEW-SHUN; BUONPANE, REBECCA
To: MEDIMMUNE LLC
Reel/Frame 045383/0409 →
Continuity (4)
Continuation 14440748
Provisional Application 61723137 · Nov 6, 2012
Provisional Application 61782405 · Mar 14, 2013
Related Publication 20190016787A1 · Jan 17, 2019
Cited By (1)
US 12,264,194