IP Library Granted Patent US 10,323,097
Granted Patent B2
US 10,323,097 · App. 15/341,550 · Granted Jun 18, 2019

Anti-C5a receptor antibodies

Inventors: Kristian Kjaergaard (Ballerup, DK); Soeren Lund (Copenhagen SV, DK); Stefan Zahn (Stenloese, DK); Louise H. Zeuthen (Birkeroed, DK); Anker J. Hansen (Charlottenlund, DK)
Assignee: Novo Nordisk A/S
C07K16/2896A61K2039/505C07K2317/21C07K2317/52C07K2317/565C07K2317/71C07K2317/76C07K2317/92
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Quick Facts
Patent No.
US 10,323,097
App. No.
15/341,550
Granted
Jun 18, 2019
Kind
B2
Abstract

The present invention concerns human antibodies recognizing the human C5a receptor. By binding to C5aR the antibodies inhibit C5a signalling, whereby the pro-inflammatory signal is inhibited. Based on the role of C5a and its receptor in stimulation of inflammation the invention further relates to therapeutic use of said human anti-C5aR antibodies and in particular in relation to treatment of immunological disorders.

Claims (35)

1. An antibody that specifically binds C5aR, wherein the antibody comprises a heavy chain variable region comprising:

a CDR1 sequence comprising SEQ ID 1, 9, 17 or 25; a CDR2 sequence comprising SEQ ID 2, 10, 18 or 26; and a CDR3 sequence comprising SEQ ID 3, 11, 19 or 27; and

wherein the antibody comprises a light chain variable region comprising:

a CDR1 sequence comprising SEQ ID 5, 13, 21 or 29; a CDR2 sequence comprising SEQ ID 6, 14, 22 or 30; and a CDR3 sequence comprising SEQ ID 7, 15, 23 or 31.

2. The antibody according to any claim 1 , wherein the antibody is selected from:

a. an antibody where the CDRs of the variable region of the heavy chain comprise SEQ ID 1, 2 and 3 and where the CDRs of the variable light chain comprise SEQ ID 5, 6 and 7;

b. an antibody where the CDRs of the variable region of the heavy chain comprise SEQ ID 9,10 and 11 and where the CDRs of the variable light chain comprises SEQ ID 13, 14 and 15;

c. an antibody where the CDRs of the variable region of the heavy chain comprise SEQ ID 17,18 and 19 and where the CDRs of the variable light chain comprises SEQ ID 21, 22 and 23;

d. an antibody where the CDRs of the variable region of the heavy chain comprise SEQ ID 25, 26 and 27 and where the CDRs of the variable light chain comprises SEQ ID 29, 30 and 31.

3. The antibody according to claim 1 , wherein the variable region of the heavy chain of said antibody comprises a sequence at least 80% identical to SEQ ID NO: 4, 12, 20 or 28 and/or wherein the variable region of the light chain of said antibody comprises a sequence at least 8094% identical to SEQ ID NO: 8, 16, 24 or 32.

4. The antibody according to claim 1 , wherein the antibody is a human antibody.

5. The antibody according to claim 1 , wherein said antibody binds the 2nd extracellular loop of human C5aR.

6. The antibody according to claim 1 wherein the affinity of the antibody as measured by competition ligand binding assay on neutrophils is below 0.80 nM.

7. The antibody according to claim 1 wherein the antibody significantly inhibits or reduces binding of C5a to C5aR.

8. The antibody according to claim 1 wherein the antibody significantly inhibits migration of human neutrophils in vitro.

9. The antibody according to claim 1 , wherein the Fc region has decreased binding affinity to one or more Fcγ receptors compared to IgG1, IgG2, IgG4 or IgG4/G2 Fc reference sequences as defined by SEQ ID NO 33, 34, 35 and 36, respectively.

10. The antibody according to claim 1 wherein the antibody does not significantly induce antibody dependent cellular cytotoxicity (ADCC), complement dependent cytotoxicity (CDC) and/or phagocytosis of neutrophils in vitro.

11. The antibody according to claim 1 wherein the Fc region is IgG1 (SEQ ID NO: 33), IgG2 (SEQ ID NO: 34), IgG2/4 (SEQ ID NO: 35), or IgG4 (SEQ ID NO: 36), with one or more of the following point mutations:

a. E233P;

b. L234A or V234A or F234L or F234V;

c. L235E or L235A;

d. G236R or G236A;

e. G237A;

f. N297Q;

g. L328R;

h. A330S;

i. P331S.

12. A method of inhibiting binding of C5a to C5aR in subject comprising administering the antibody of claim 1 to said subject, thereby inhibiting binding of C5a to C5aR in the subject.

13. The method of claim 12 , wherein the subject has an inflammatory or immunological disease or disorder.

14. A method of inhibiting hC5a mediated neutrophil migration in a subject comprising administering the antibody of claim 1 to said subject, thereby inhibiting hC5a mediated neutrophil migration in the subject.

15. The method of claim 14 , wherein the subject has an inflammatory or immunological disease or disorder.

16. A method of inhibiting binding of C5a to C5aR in subject comprising administering the antibody of claim 2 to said subject, thereby inhibiting binding of C5a to C5aR in the subject.

17. The method of claim 16 , wherein the subject has an inflammatory or immunological disease or disorder.

18. A method of inhibiting hC5a mediated neutrophil migration in a subject comprising administering the antibody of claim 2 to said subject, thereby inhibiting hC5a mediated neutrophil migration in the subject.

19. The method of claim 18 , wherein the subject has an inflammatory or immunological disease or disorder.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 11, 2019
From: PADKJAER, SOEREN BERG
To: NOVO NORDISK A/S
Reel/Frame 049731/0493 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 11, 2019
From: ZAHN, STEFAN; ZEUTHEN, LOUISE HJERRILD; HANSEN, ANKER JON; KJAERGAARD, KRISTIAN; LUND, SOEREN
To: NOVO NORDISK A/S
Reel/Frame 049731/0663 →
Priority Claims (2)
EP 11168787 · Jun 6, 2011 · regional
EP 12159172 · Mar 13, 2012 · regional
Continuity (5)
Continuation 14467393 · Aug 25, 2014
Continuation 13920585 · Jun 18, 2013
Continuation 13490093
Provisional Application 61505137 · Jul 7, 2011
Related Publication 20170073421A1 · Mar 16, 2017
Cited By (4)
US 12,187,807 US 12,227,587 US 12,264,203 US 12,415,865