IP Library Granted Patent US 10,329,536
Granted Patent B2
US 10,329,536 · App. 10/487,707 · Granted Jun 25, 2019

Methods for producing an active constituent of a pharmaceutical or a diagnostic agent in an MDCK cell suspension culture

Inventors: Jürgen Vorlop (Marburg, DE); Christian Frech (Mannheim, DE); Holger Lübben (Wetter, DE); Jens-Peter Gregersen (Wetter, DE)
Assignee: Seqirus UK Limited
C12N7/00A61K39/00A61K2039/5252C12N2710/10051C12N2710/16651C12N2710/16751C12N2710/24151C12N2720/12051C12N2720/12351C12N2760/16251C12N2760/18051C12N2760/18551C12N2760/20151C12N2770/24151Y02A50/386Y02A50/388Y02A50/39Y02A50/464Y02A50/466
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Quick Facts
Patent No.
US 10,329,536
App. No.
10/487,707
Granted
Jun 25, 2019
Kind
B2
Abstract

The present invention concerns a method for production of an active ingredient of a drug or diagnostic agent, in which (a) MDCK cells are infected with a virus; and (b) the MDCK cells are cultured in suspension culture on a commercial scale under conditions that permit multiplication of the viruses; in which culturing occurs in a volume of at least 30 L. The invention also concerns a method for production of a drug or diagnostic agent in which an active ingredient is produced according to the above method and mixed with an appropriate adjuvant, auxiliary, buffer, diluent or drug carrier.

Claims (15)

1. A method for production of a virus or a protein produced from the virus for use in manufacture of a viral vaccine on a commercial scale, comprising:

(a) increasing the volume of a suspension culture of Madin-Darby Canine Kidney (MDCK) cells in a serum-free medium, a protein-free medium, or a chemically defined medium, in a fed-batch system by diluting with fresh medium to the suspension culture to increase its volume to at least 1000 L without removal of the original medium, wherein the fresh medium is added to the original medium to increase the volume of the suspension culture to the at least 1000 L such that the dilution is 1:10 to 1:2 original medium to fresh medium,

(b) infecting the MDCK cells in the at least 1000 L volume with the virus,

(c) propagating the viruses in the MDCK suspension culture, and

(d) isolating the viruses or a protein produced from the viruses from the cell culture, wherein the virus is selected from the group consisting of an adenovirus, orthomyxovirus, paramyxovirus, reovirus, picornavirus, enterovirus, flavivirus, herpes virus and pox virus.

2. The method according to claim 1 , wherein the MDCK cells in the suspension culture originate from the cell line MDCK 33016.

3. The method according to claim 1 or 2 , wherein the virus selected is a dsDNA, RNA(+), or RNA(−) virus and is an adenovirus, orthomyxovirus, paramyxovirus, reovirus, picornavirus, enterovirus, flavivirus, herpes virus or pox virus.

4. The method according to claim 1 or 2 , wherein the cells are cultured in a chemically defined medium before infection and in a protein free medium after infection.

5. The method according to claim 1 or 2 , further comprising purifying the virus by Cellufine Sulfate (CS) chromatography and/or ultracentrifugation in a sucrose gradient.

6. The method of claim 1 or 2 , wherein the vaccine is mixed with an appropriate adjuvant, auxiliary, buffer, diluent or drug carrier.

7. A method for production of a virus or a protein produced from the virus for use in manufacture of a viral vaccine on a commercial scale, comprising:

(a) increasing the volume of a suspension culture of Madin-Darby Canine Kidney (MDCK) cells in a serum-free medium, a protein-free medium, or a chemically defined medium, in a fed-batch system by diluting with fresh medium to the suspension culture to increase its volume to at least 1000 L without removal of the original medium, wherein the fresh medium is added to the original medium to increase the volume of the suspension culture to the at least 1000 L such that the dilution is 1:10 to 1:2 original medium to fresh medium,

(b) infecting the MDCK cells in the at least 1000 L volume with the virus,

(c) propagating the viruses in the MDCK suspension culture, and

(d) isolating the viruses or a protein produced from the viruses from the cell culture, wherein the virus is an influenza virus and the influenza virus used in step (b) is from a primary isolate that was pre-multiplied in cell culture to produce a pure isolate.

Assignments (5)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 2, 2019
From: NOVARTIS AG
To: SEQIRUS UK LIMITED
Reel/Frame 049058/0825 →
CHANGE OF NAME Recorded May 29, 2013
From: NOVARTIS VACCINES AND DIAGNOSTICS GMBH & CO. KG
To: NOVARTIS VACCINES AND DIAGNOSTICS GMBH
Reel/Frame 030506/0356 →
CHANGE OF NAME Recorded May 29, 2013
From: CHIRON BEHRING GMBH & CO.
To: NOVARTIS VACCINES AND DIAGNOSTICS GMBH & CO. KG
Reel/Frame 030508/0168 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 27, 2012
From: NOVARTIS VACCINES AND DIAGNOSTICS GMBH
To: NOVARTIS AG
Reel/Frame 028456/0165 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 5, 2007
From: VORLOP, JURGEN; GREGERSEN, JEN-PETER; FRECH, CHRISTIAN; LUBBEN, HOLGER
To: CHIRON BEHRING GMBH & CO.
Reel/Frame 020071/0175 →
Priority Claims (1)
DE 101 44 906 · Sep 12, 2001 · national
Continuity (1)
Related Publication 20050118140A1 · Jun 2, 2005
Cited By (1)
US 12,667,612