IP Library Granted Patent US 9,212,349
Granted Patent B2
US 9,212,349 · App. 14/112,824 · Granted Dec 15, 2015

Method to produce virus in cultured cells

Inventors: Thomas Shenk (Princeton, NJ); Emre Koyuncu (Princeton, NJ); Joshua D. Rabinowitz (Princeton, NJ)
Assignee: THE TRUSTEES OF PRINCETON UNIVERSITY
C12N7/00C12N2710/16151C12N2710/16751
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Quick Facts
Patent No.
US 9,212,349
App. No.
14/112,824
Granted
Dec 15, 2015
Kind
B2
Abstract

A method for improving virus production in a host cell infected with the virus is provided.

Claims (16)

1. A method for producing a virus comprising:

culturing a host cell infected with a virus under conditions appropriate for producing the virus, wherein:

the conditions include post-infection addition of supplemental fatty acid of at least 20 carbon atoms and a carbonyl and/or a free radical scavenging compound in amounts and for a time effective to improve the amount of virus production compared to virus produced in the method performed without the supplemental fatty acid and scavenger compound.

2. The method of claim 1 , wherein the fatty acid is selected from the group consisting of eicosapentaenoic acid (EPA), docosahexaenoic acid (DHA), arachidonic acid (AA), hexacosanoic acid (HSA) and octacosanoic acid, OSA).

3. The method of claim 1 , wherein:

the addition further includes cholesterol, and

the virus is produced in an amount greater in the presence of the supplemental fatty acid, scavenger and cholesterol compared to virus produced in the method performed without the supplemental fatty acid, scavenger and cholesterol.

4. The method of claim 2 , wherein:

the addition further includes cholesterol, and

the virus is produced in an amount greater in the presence of the supplemental fatty acid, scavenger and cholesterol compared to virus produced in the method performed without the supplemental fatty acid, scavenger and cholesterol.

5. The method of claim 1 , wherein the carbonyl and/or a free radical scavenging compound is selected from the group consisting of aminoguanidine, alpha-tocopherol, hydralazine, glycosylisovitexin, N-acetyl-cystein, metformin, penicillamine, pyridoxamine, edaravone (EDA), tenilsetam, lipoic acid, 3,3-dimethyl-D-cysteine (DMC), L-3,3-dimethyl-D-cysteine (L-DMC), N-acetyl-3,3-dimethyl-D-cysteine (ADMC), Nα-acetyl-L-cysteine (NAC), 3,3-dimethyl-D-cysteine-disulfide (DMCSS), S-methyl-DMC (SMDMC), L-cysteine (CYS), L-cysteine-O-methylester (CYSM), 3,3-dimethyl-D-cysteine-methylester (DMCM), 3-methyl-3-ethyl-D-cysteine (MEC), semicarbazide hydrochloride SC (hydrazine carboxamide), 1,1-dimethyl-biguanide hydrochloride (DMBG), N-tertbutylhydroxylamine(BHA), a flavonoid, a flavanol, epicatechin, a flavanone, naringenin, a flavonol, quercetin, a flavones, luteolin, an isoflavone, genistein, an anthocyanidin, cyanidin, a phenol/phenolic acid, a flavan-3-ol compound, procyanidins B1 (9.8), procyanidins B2, (+)-catechin, (−)-epicatechin, caftaric acid, caffeic acid, and kaempferol.

6. The method of claim 5 , wherein the carbonyl and/or a free radical scavenging compound is aminoguanidine or alpha-tocopherol.

7. The method of claim 2 , wherein the scavenging compound is selected from the group consisting of aminoguanidine, alpha-tocopherol, hydralazine, glycosylisovitexin, N-acetyl-cystein, metformin, penicillamine, pyridoxamine, edaravone (EDA), tenilsetam, lipoic acid, 3,3-dimethyl-D-cysteine (DMC), L-3,3-dimethyl-D-cysteine (L-DMC), N-acetyl-3,3-dimethyl-D-cysteine (ADMC), Nα-acetyl-L-cysteine (NAC), 3,3-dimethyl-D-cysteine-disulfide (DMCSS), S-methyl-DMC (SMDMC), L-cysteine (CYS), L-cysteine-O-methylester (CYSM), 3,3-dimethyl-D-cysteine-methylester (DMCM), 3-methyl-3-ethyl-D-cysteine (MEC), semicarbazide hydrochloride SC (hydrazine carboxamide), 1,1-dimethyl-biguanide hydrochloride (DMBG), N-tertbutylhydroxylamine(BHA), a flavonoid, a flavanol, epicatechin, a flavanone, naringenin, a flavonol, quercetin, a flavones, luteolin, an isoflavone, genistein, an anthocyanidin, cyanidin, a phenol/phenolic acid, a flavan-3-ol compound, procyanidins B1 (9.8), procyanidins B2, (+)-catechin, (−)-epicatechin, caftaric acid, caffeic acid, and kaempferol.

8. The method of claim 7 , wherein the scavenging compound is aminoguanidine or alpha-tocopherol.

9. The method of claim 3 , wherein the carbonyl and/or a free radical scavenging compound is selected from the group consisting of aminoguanidine, alpha-tocopherol, hydralazine, glycosylisovitexin, N-acetyl-cystein, metformin, penicillamine, pyridoxamine, edaravone (EDA), tenilsetam, lipoic acid, 3,3-dimethyl-D-cysteine (DMC), L-3,3-dimethyl-D-cysteine (L-DMC), N-acetyl-3,3-dimethyl-D-cysteine (ADMC), Nα-acetyl-L-cysteine (NAC), 3,3-dimethyl-D-cysteine-disulfide (DMCSS), S-methyl-DMC (SMDMC), L-cysteine (CYS), L-cysteine-O-methylester (CYSM), 3,3-dimethyl-D-cysteine-methylester (DMCM), 3-methyl-3-ethyl-D-cysteine (MEC), semicarbazide hydrochloride SC (hydrazine carboxamide), 1,1-dimethyl-biguanide hydrochloride (DMBG), N-tertbutylhydroxylamine(BHA), a flavonoid, a flavanol, epicatechin, a flavanone, naringenin, a flavonol, quercetin, a flavones, luteolin, an isoflavone, genistein, an anthocyanidin, cyanidin, a phenol/phenolic acid, a flavan-3-ol compound, procyanidins B1 (9.8), procyanidins B2, (+)-catechin, (−)-epicatechin, caftaric acid, caffeic acid, and kaempferol.

10. The method of claim 9 , wherein the carbonyl and/or a free radical scavenging compound is aminoguanidine or alpha-tocopherol.

Assignments (2)
CONFIRMATORY LICENSE Recorded Jan 29, 2014
From: PRINCETON UNIVERSITY
To: NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT
Reel/Frame 032140/0803 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 30, 2013
From: SHENK, THOMAS; KOYUNCU, EMRE; RABINOWITZ, JOSHUA D.
To: THE TRUSTEES OF PRINCETON UNIVERSITY
Reel/Frame 031860/0167 →
Continuity (2)
Provisional Application 61476497 · Apr 18, 2011
Related Publication 20140113353A1 · Apr 24, 2014