IP Library Granted Patent US 10,851,150
Granted Patent B2
US 10,851,150 · App. 16/044,252 · Granted Dec 1, 2020

Carbohydrate content of CTLA4 molecules

Inventors: Kirk J. Leister (Fayetteville, NY); Eugene J. Schaefer (Westfield, NJ); Ronald Charles Bates (Irvine, CA); Elizabeth A. Bramhall (Groton, MA); David Michael Didio (Syracuse, NY); Robert Donaldson (Southborough, MA); Alan R. Flesher (Lawrenceville, NJ); Helen Gray Haggerty (Manlius, NY); David Henry Kirkley (East Syracuse, NY); John Malcolm Tabor (Syracuse, NY); Lee K. Tay (Princeton Junction, NJ); Pallaiah Thammana (Manlius, NY); Ajoy Velayudhan (Cary, NC); David Edward Smolin (Pennington, NJ); Reb J. Russell (Doylestown, PA); Thomas James Vanden Boom (Flemington, NJ); Dean Woodrow Brownell (Oswego, NY); Jeffrey Schrimsher (Hillsborough, NC); Joyce Patricia Whitehead (Manlius, NY)
Assignee: Bristol-Myers Squibb Company
C07K14/70521A61K38/195C07K16/2818A61K38/00B01D15/3804C07K2317/73C07K2317/76C07K2319/30
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Quick Facts
Patent No.
US 10,851,150
App. No.
16/044,252
Granted
Dec 1, 2020
Kind
B2
Abstract

The invention provides for mammalian cells capable of producing recombinant CTLA4-Ig and variants thereof. The invention also provides for compositions comprising CTLA4-Ig and formulations thereof. The invention further provides for methods for mass-producing CTLA4-Ig from mammalian cells capable of producing this recombinant protein, and for purifying the CTLA4-Ig.

Claims (23)

1. A composition comprising CTLA4 A29YL104E -Ig molecules comprising:

(a) an average molar ratio of sialic acid to CTLA4 A29YL104E -Ig molecules of at least about 5;

(b) an average molar ratio of N-acetyl neuraminic acid (NANA) to CTLA4 A29YL104E -Ig molecules of from about 5 to about 10;

(c) an average molar ratio of N-glycolyl neuraminic acid (NGNA) to CTLA4 A29YL104E -Ig molecules less than or equal to 1.5;

(d) an average molar ratio of N-Acetylgalactosamine (GalNAc) to CTLA4 A29YL104E -Ig molecules from about 2.7 to about 3.6;

(e) an average molar ratio of N-Acetylglucosamine (GlcNAc) to CTLA4 A29YL104E -Ig molecules from about 24 to about 28;

(f) an average molar ratio of galactose to CTLA4 A29YL104E -Ig molecules from about 9.2 to about 17;

(g) an average molar ratio of fucose to CTLA4 A29YL104E -Ig molecules from about 4.2 to about 7.0;

(h) an average molar ratio of mannose to CTLA4 A29YL104E -Ig molecules from about 10 to about 20;

and

(i) less than or equal to 5.0 area percent high molecular weight species as determined by size exclusion chromatography and spectrophotometric detection,

wherein the CTLA4 A29YL104E -Ig molecules comprise one or more CTLA4 A29YL104E -Ig polypeptides having the amino acid sequence set forth in SEQ ID NO: 4, 11, 12, 13, 14, 15, or 16.

2. The CTLA4 A29YL104E composition of claim 1 , wherein the concentration of MCP-1 in the CTLA4 A29YL104E -Ig composition is less than about 5 ppm.

3. The CTLA4 A29YL104E composition of claim 1 , wherein the CTLA4 A29YL104E -Ig composition comprises at least 95% of dimeric CTLA4 A29YL104E -Ig forms.

4. The CTLA4 A29YL104E -Ig composition of claim 1 , wherein the CTLA4 A29YL104E -Ig composition comprises less than or equal to 4.0 area percent high molecular weight species as determined by size exclusion chromatography and spectrophotometric detection.

5. The CTLA4 A29YL104E -Ig composition of claim 1 , wherein the CTLA4 A29YL104E -Ig composition comprises less than or equal to 3.0 area percent high molecular weight species as determined by size exclusion chromatography and spectrophotometric detection.

6. The CTLA4 A29YL104E -Ig composition of claim 1 , wherein the CTLA4 A29YL104E -Ig composition comprises less than or equal to 2.5 area percent high molecular weight species as determined by size exclusion chromatography and spectrophotometric detection.

7. The CTLA4 A29YL104E -Ig composition of claim 1 , wherein the CTLA4 A29YL104E -Ig composition comprises less than or equal to 2.0 area percent high molecular weight species as determined by size exclusion chromatography and spectrophotometric detection.

8. The CTLA4 A29YL104E -Ig composition of claim 1 , wherein the CTLA4 A29YL104E -Ig composition comprises a polypeptide having the amino acid sequence set forth in SEQ ID NO: 16.

9. The CTLA4 A29YL104E -Ig composition of claim 1 , wherein (a) about 90% of the CTLA4 A29YL104E -Ig polypeptides are polypeptides of SEQ ID NO: 13 or 16, or any combination thereof;

(b) about 10% of the CTLA4 A29YL104E -Ig polypeptides are polypeptides of SEQ ID NO: 12 or 15, or any combination thereof;

(c) about 4% of the CTLA4 A29YL104E -Ig polypeptides are polypeptides of SEQ ID NO:4, 11, 12, or 13, or any combination thereof; and,

(d) about 96% of the CTLA4 A29YL104E -Ig polypeptides are polypeptides of SEQ ID NO: 14, 15, or 16, or any combination thereof.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 27, 2020
From: LEISTER, KIRK J.; SCHAEFER, EUGENE J.; BATES, RONALD CHARLES; BRAMHALL, ELIZABETH A.; DIDIO, DAVID MICHAEL; DONALDSON, ROBERT; FLESHER, ALAN R.; HAGGERTY, HELEN GRAY; KIRKLEY, DAVID HENRY; TABOR, JOHN MALCOLM; TAY, LEE K.; THAMMANA, PALLAIAH; VELAYUDHAN, AJOY; SMOLIN, DAVID EDWARD; RUSSELL, REB J.; BOOM, THOMAS JAMES VANDEN; BROWNELL, DEAN WOODROW; SCHRIMSHER, JEFFREY; WHITEHEAD, JOYCE PATRICIA
To: BRISTOL-MYERS SQUIBB COMPANY
Reel/Frame 052504/0730 →
Continuity (7)
Division 16042977 · Jul 23, 2018
Division 12086786
Provisional Application 60752267 · Dec 20, 2005
Provisional Application 60752150 · Dec 20, 2005
Provisional Application 60849543 · Oct 5, 2006
Related Publication 20190092836A1 · Mar 28, 2019
Related Publication 20200017569A9 · Jan 16, 2020