IP Library Patent Application 17557921
Patent Application
App. No. 17/557,921

METHODS FOR REDUCING THE OXIDATION LEVEL OF CYSTEINE RESIDUES IN A SECRETED RECOMBINANTLY-EXPRESSED PROTEIN DURING CELL CULTURE

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Patent No.
US None
App. No.
17/557,921
Abstract

The present disclosure relates to methods for reducing the oxidation level of cysteine residues in recombinant polypeptides such as anti-IL-17 antibodies during cell culture (e.g., a preparation of secukinumab antibodies) that have been recombinantly produced by mammalian cells. Also provided are purified preparations of recombinant polypeptides such as anti-IL-17 antibodies or antigen binding fragments thereof produced by such methods, e.g, purified preparations of secukinumab. Also provided are purified preparations of recombinant polypeptides produced by such methods wherein the level of active recombinant polypeptide in the preparation is high.

Claims (33)

1 . A process for the production of a recombinant polypeptide in a fed batch cell culture, comprising the steps of:

a. culturing mammalian cells in a cell culture medium comprising a base medium and one or more feed media, wherein the base medium comprises a concentration of cys equivalents of about 0.3 g/L and wherein the feed media comprises a concentration of cys equivalents of less than about 0.8 g/L, and wherein the concentration of cumulative cys equivalents in the cell culture media are less than about 0.4 g/L;

b. expressing the recombinant polypeptide and

c. recovering the polypeptide from the culture medium, wherein the recombinant polypeptide is an antibody.

2 . The process according to claim 1 , wherein the base medium comprises no added cysteine and the feed media comprise a concentration of cysteine of about 0.66 g/L.

3 . The process according to claim 1 , wherein the base medium comprises no added cysteine and the feed media comprise a concentration of cysteine of about 0.33 g/L.

4 . The process according to claim 1 , wherein the base medium comprises no added cysteine and the feed media comprise no cysteine.

5 . (canceled)

6 . The process according to claim 1 , wherein the antibody is secukinumab.

7 . The process according to claim 1 , wherein the mammalian cells are selected from the group consisting of CHO cells, HEK cells and SP2/0 cells.

8 . The process according to claim 1 , comprising a downstream processing step of selective reduction, wherein the antibody is incubated with at least one reducing agent in a system to form a reducing mixture.

9 . (canceled)

10 . The process according to claim 1 , wherein the antibody comprises at least one disulfide bond and at least one free cysteine.

11 . (canceled)

12 . The process according to claim 10 , wherein the antibody is secukinumab.

13 . The process according to claim 1 , wherein a population of recombinant antibody polypeptides recovered from the culture medium comprises at least about a 10% higher level of reduced free cysteine as compared to a population of recombinant antibody polypeptides recovered from control culture media, the control culture media comprising a control base medium having a concentration of cys equivalents of greater than about 0.4 g/L and/or control feed media comprising a concentration of cys equivalents of greater than about 0.9 g/L, and/or wherein the concentration of cumulative cys equivalents in the control cell culture are greater than about 0.4 g/L.

14 . The process according to claim 1 , wherein the process comprises producing a higher yield, in mg of recombinant antibody polypeptide per L of culture media, of recombinant antibody polypeptide as compared to a control process comprising culturing mammalian cells in a control cell culture media comprising a control base medium and one or more control feed media, wherein the control base medium comprises a concentration of cys equivalents of greater than about 0.4 g/L and/or wherein the control feed media comprises a concentration of cys equivalents of greater than about 0.9 g/L, and/or wherein the concentration of cumulative cys equivalents in the control cell culture are greater than about 0.4 g/L.

15 . The process according to claim 13 , wherein the process comprises producing a population of recombinant antibody polypeptides having at least 61% reduced free cysteine as assayed from spent culture media.

16 . A process for the production of a recombinant polypeptide by mammalian cell culture, comprising the steps of:

a. providing a culture comprising a cell culture medium and mammalian cells selected from the group consisting of CHO cells, HEK cells and SP2/0 cells, wherein the culture medium comprises a concentration of cys equivalents of about 0.3 g/L;

b. culturing mammalian cells;

c. exchanging a portion of the cell culture medium in the culture with fresh cell culture medium by perfusion, wherein the fresh cell culture medium comprises a concentration of cys equivalents of about 0.3 g/L, and/or wherein the concentration of cumulative cys equivalents added to the culture are less than about 7 g/L, or less than about 0.4 g/L per day;

d. expressing the recombinant polypeptide and

e. recovering the polypeptide from the culture,

wherein the recombinant polypeptide is an antibody.

17 . The process according to claim 16 , wherein the fresh culture medium comprises no added cysteine.

18 . The process according to claim 16 , wherein the process comprises exchanging at least 50% of the cell culture media with fresh cell culture medium by perfusion per day of culturing.

19 . The process according to claim 16 , wherein the recombinant antibody polypeptide comprises at least one free cysteine and at least one disulfide bond.

20 . (canceled)

21 . The process according to claim 16 , wherein the recombinant antibody polypeptide is secukinumab.

22 . The process according to claim 16 , wherein a population of recombinant antibody polypeptides recovered from the culture medium comprises at least about a 10% higher level of reduced free cysteine as compared to a population of recombinant antibody polypeptides recovered from a control culture media, the control culture media comprising a concentration of cys equivalents of greater than about 0.4 g/L and/or wherein the concentration of cumulative cys equivalents added to the control cell culture are greater than about 7 g/L, and/or greater than about 0.4 g/L per day.

23 . The process according to claim 16 , wherein the process comprises producing a higher yield, in mg of recombinant antibody polypeptide per L of culture media, of recombinant antibody polypeptide as compared to a control process comprising culturing mammalian cells in a control cell culture medium, wherein the control cell culture medium comprises a concentration of cys equivalents of greater than about 0.4 g/L, and/or wherein the concentration of cumulative cys equivalents in the control cell culture media are greater than about 7 g/L, and/or greater than about 0.4 g/L per day.

24 . The process according to claim 1 , wherein the process further comprises covalently modifying the reduced free cysteine with a linker, a label, or a drug.

Assignments (6)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 11, 2026
From: NOVARTIS AG
To: NOVARTIS PHARMA AG
Reel/Frame 075712/0291 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 4, 2022
From: NOVARTIS INSTITUTES FOR BIOMEDICAL RESEARCH, INC.
To: NOVARTIS AG
Reel/Frame 058891/0918 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 14, 2022
From: CARINHAS, NUNO BUXO; GARCIA, DAVID; GOEBEL, MATHIAS
To: NOVARTIS PHARMA AG
Reel/Frame 058658/0520 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 14, 2022
From: SHULTZ, JOSEPH
To: NOVARTIS PHARMA AG
Reel/Frame 058658/0624 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 14, 2022
From: CUI, HUANCHUN
To: NOVARTIS INSTITUTES FOR BIOMEDICAL RESEARCH, INC.
Reel/Frame 058658/0770 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 14, 2022
From: NOVARTIS PHARMA AG
To: NOVARTIS AG
Reel/Frame 058774/0052 →