IP Library Granted Patent US 46,585
Granted Patent E1
US 46,585 · App. 14/993,277 · Granted Oct 24, 2017

Optimized FC variants

Inventors: Christian Behrens (Vauhallan, FR); Sylvie Jorieux (Lomme, FR); Abdelhakim Kharrat (Montgiscard, FR); Khalil Bouayadi (Ramonville Saint Agne, FR); Philippe Mondon (Neuve Chapelle, FR); Celine Monnet-Mars (Lambersart, FR)
Assignee: LABORATOIRE FRANCAIS DU FRACTIONNEMENT ET DES BIOTECHNOLOGIES
C07K16/00C07K2317/21C07K2317/52C07K2317/92
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 46,585
App. No.
14/993,277
Granted
Oct 24, 2017
Kind
E1
Abstract

A variant of a parent polypeptide including an Fc region, which variant exhibits increased binding to FcRn as compared to the parent polypeptide and includes at least one amino acid modification in the Fc region.

Claims (47)

1. A variant of a parent polypeptide comprising a Fc region, which variant exhibits increased binding to FcRn as compared to said parent polypeptide and comprises

a combination of amino acid modifications selected from the group consisting of:

N315D/A330V/N361D/A378V/N434Y,

V264E/N315D/A378V/N390S/G420R/N434Y,

N315D/A378V/N434Y,

N315D/A330V/A378V/N434Y,

N315D/K334E/A378V/N434Y,

V264E/N315D/A378V,

P228R/N315D/A330V/N361D/A378V/N434Y,

P228R/P230S/N315D/A330V/N361D/A378V/N434Y,

P228L/N315D/A330V/N361D/A378V/N434Y,

P228L/P230S/N315D/A330V/N361D/A378V/N434Y,

P230S/N315D/A330V/N361D/A378V/N434Y, and

P230T/V264E/N315D/K370R/A378V

of the Fc region, wherein the numbering of the amino acids in the Fc region is that of the EU index as in Kabat.

2. The variant according to claim 1 , wherein said variant is an antibody.

3. The variant according to claim 2 , wherein said antibody is an IgG antibody.

4. A pharmaceutical composition comprising a variant as defined in claim 1 .

5. A medicament comprising a variant according to claim 1 .

6. An isolated nucleic acid encoding a variant as defined in claim 1 .

7. A vector comprising the nucleic acid of claim 6 .

8. An isolated host cell containing the vector of claim 7 .

9. A method for producing a variant according to claim 1 , comprising culturing a host cell containing a vector comprising an isolated nucleic acid encoding said variant so that the nucleic acid is expressed.

10. A variant of a parent polypeptide comprising a Fc region, which variant exhibits increased binding to FcRn as compared to said parent polypeptide and comprises from 2 to 7 amino acid modifications, said amino acid modifications comprising:

(i) one amino acid modification selected from the group consisting of 434Y and 434S, and

(ii) at least one amino acid modification selected from the group consisting of 226G, P228L, P228R, 230S, 230T, 230L, 241L, 264E, 307P, 315D, 330V, 362R, 378V, 378T, 389T, 389K, 434Y and 434S

of the Fc region, wherein the numbering of the amino acids in the Fc region is that of the EU index as in Kabat and with the proviso that the modification (i) does not occur at the same amino acid position as the modification (ii).

11. The variant according to claim 10, said variant comprising at least one combination of amino acid modifications selected from the group consisting of:

226G/315D/434Y, 230S/315D/434Y, 230T/315D/434Y, 230T/264E/434S, 230T/389T/434S, 241L/264E/434S, 250A/389K/434Y, 259I/315D/434Y, 264E/378V/434S, 264E/396L/434S, 294del/307P/434Y, 307P/378V/434Y, 315D/330V/434Y, 315D/382V/434Y and 378V/383N/434Y of the Fc region as compared to said parent polypeptide, wherein the numbering of the amino acids in the Fc region is that of the EU index as in Kabat.

12. The variant according to claim 11, wherein the said variant further comprises at least one amino acid modification selected from the group consisting of 226G, 227L, 230S, 230T, 230L, 231T, 241L, 243L, 250A, 256N, 259I, 264E, 265G, 267R, 290E, 294del, 303A, 305A, 307P, 307A, 308I, 315D, 322R, 325S, 327V, 330V, 342R, 347R, 352S, 361D, 362R, 362E, 370R, 378V, 378T, 382V, 383N, 386R, 386K, 387T, 389T, 389K, 392R, 395A, 396L, 397M, 403T, 404L, 415N, 416K, 421T, 426T, 428L, 433R, 434Y, 434S and 439R of the Fc region, as compared to the parent polypeptide, wherein the numbering of the amino acids in the Fc region is that of the EU index as in Kabat.

13. The variant according to claim 10, wherein the said variant comprises one combination of amino acid modifications selecting from the group consisting of 307A/315D/330V/382V/389T/434Y, 256N/378V/383N/434Y, 315D/330V/361D/378V/434Y, 259I/315D/434Y, 230S/315D/428L/434Y, 250A/389K/434Y, 305A/315D/330V/395A/434Y, 264E/386R/396L/434S/439R, 315D/330V/362R/434Y, 294del/307P/434Y, 305A/315D/330V/389K/434Y, 315D/327V/330V/397M/434Y, 264E/396L/415N/434S, 227L/264E/378V/434S, 230T/315D/362R/426T/434Y, 226G/315D/330V/434Y, 250A/315D/325S/330V/434Y, 290E/315D/342R/382V/434Y, 241L/315D/330V/392R/434Y, 241L/264E/307P/378V/434S, 230T/264E/403T/434S, 230T/315D/362E/434Y, 226G/315D/434Y, 226G/315D/362R/434Y, 226G/264E/347R/370R/378V/434S, 308I/315D/330V/382V/434Y, 230T/264E/378V/434S, 231T/241L/264E/378T/397M/434S, 230L/264E/378V/434S, 230T/315D/330V/386K/434Y, 226G/315D/330V/389T/434Y, 267R/307P/378V/421T/434Y, 230S/315D/387T/434Y, 230S/264E/352S/378V/434S and 230T/303A/322R/389T/404L/434S of the Fc region as compared to said parent polypeptide, wherein the numbering of the amino acids in the Fc region is that of the EU index as in Kabat.

14. The variant according to claim 13, wherein the said variant comprises a combination of amino acid modifications selecting from the group consisting of:

T307A/N315D/A330V/E382V/N389T/N434Y,

T256N/A378V/S383N/N434Y,

N315D/A330V/N361D/A378V/N434Y,

V259I/N315D/N434Y,

P230S/N315D/M428L/N434Y, and

E294del/T307P/N434Y,

of the Fc region, wherein the numbering of the amino acids in the Fc region is that of the EU index as in Kabat.

15. The variant according to claim 14, wherein said variant is an antibody.

16. The variant according to claim 15, wherein said antibody is an IgG antibody.

17. A pharmaceutical composition comprising a variant as defined in claim 13.

18. An isolated nucleic acid encoding a variant as defined in claim 13.

19. A vector comprising the nucleic acid of claim 18.

20. An isolated host cell containing the vector of claim 19.

21. A method for producing a variant according to claim 13, comprising culturing a host cell containing a vector comprising an isolated nucleic acid encoding said variant so that the nucleic acid is expressed.

22. A variant according to claim 10, wherein the Fc region of the of a parent polypeptide is SEQ ID NO: 1 or SEQ ID NO: 2.

Assignments (4)
CHANGE OF OWNER/APPLICANT'S ADDRESS Recorded Apr 3, 2023
From: LABORATOIRE FRANÇAIS DU FRACTIONNEMENT ET DES BIOTECHNOLOGIES
To: LABORATOIRE FRANÇAIS DU FRACTIONNEMENT ET DES BIOTECHNOLOGIES
Reel/Frame 063237/0439 →
CHANGE OF OWNER/APPLICANT'S ADDRESS Recorded Sep 21, 2022
From: LABORATOIRE FRANÇAIS DU FRACTIONNEMENT ET DES BIOTECHNOLOGIES
To: LABORATOIRE FRANÇAIS DU FRACTIONNEMENT ET DES BIOTECHNOLOGIES
Reel/Frame 061493/0885 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 14, 2017
From: BEHRENS, CHRISTIAN; JORIEUX, SYLVIE; KHARRAT, ABDELHAKIM; BOUAYADI, KHALIL; MONDON, PHILIPPE; MONNET-MARS, CELINE
To: LFB BIOTECHNOLOGIES
Reel/Frame 043007/0528 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 14, 2017
From: LFB BIOTECHNOLOGIES
To: LABORATOIRE FRANCAIS DU FRACTIONNEMENT ET DES BIOTECHNOLOGIES
Reel/Frame 043007/0722 →
Priority Claims (1)
EP 09305250 · Mar 20, 2009 · regional
Continuity (3)
Reissue 13257502 · Mar 19, 2010
Continuation 14338413 · Jul 23, 2014
Reissue 13257502 · Mar 19, 2010