U.S. patents available from 1976 to present.
U.S. patent applications available from 2005 to present.

Production of vaccines

Patent 7192759 Issued on March 20, 2007. Estimated Expiration Date: Icon_subject November 26, 2019. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

Patent References

DNA sequences encoding erythropoietin
Patent #: 4703008
Issued on: 10/27/1987
Inventor: Lin

Erythropoietin composition
Patent #: 4835260
Issued on: 05/30/1989
Inventor: Shoemaker

Process for controlling intracellular glycosylation of proteins
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Inventor: Paulson, et al.

Infectious bursal disease virus production in continuous cell lines
Patent #: 5192539
Issued on: 03/09/1993
Inventor: Van Der Marel, et al.

Production of recombinant erythropoietin
Patent #: 5441868
Issued on: 08/15/1995
Inventor: Lin

Muteins of human erythropoietin, the preparation thereof and the use thereof
Patent #: 5457089
Issued on: 10/10/1995
Inventor: Fibi, et al.

଱-3 sialyltransferase
Patent #: 5494790
Issued on: 02/27/1996
Inventor: Sasaki, et al.

High level recombinant protein production using conditional helper-free adenovirus vector
Patent #: 5518913
Issued on: 05/21/1996
Inventor: Massie, et al.

Agonist peptide dimers
Patent #: 5767078
Issued on: 06/16/1998
Inventor: Johnson, et al.

Compounds and peptides that bind to the erythropoietin receptor
Patent #: 5773569
Issued on: 06/30/1998
Inventor: Wrighton, et al.

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Inventors

Assignee

Application

No. 09449854 filed on 11/26/1999

US Classes:

435/235.1, VIRUS OR BACTERIOPHAGE, EXCEPT FOR VIRAL VECTOR OR BACTERIOPHAGE VECTOR; COMPOSITION THEREOF; PREPARATION OR PURIFICATION THEREOF; PRODUCTION OF VIRAL SUBUNITS; MEDIA FOR PROPAGATING435/69.1, Recombinant DNA technique included in method of making a protein or polypeptide435/320.1, VECTOR, PER SE (E.G., PLASMID, HYBRID PLASMID, COSMID, VIRAL VECTOR, BACTERIOPHAGE VECTOR, ETC.) BACTERIOPHAGE VECTOR, ETC.)530/300, PEPTIDES OF 3 TO 100 AMINO ACID RESIDUES530/350, PROTEINS, I.E., MORE THAN 100 AMINO ACID RESIDUES435/325ANIMAL CELL, PER SE (E.G., CELL LINES, ETC.); COMPOSITION THEREOF; PROCESS OF PROPAGATING, MAINTAINING OR PRESERVING AN ANIMAL CELL OR COMPOSITION THEREOF; PROCESS OF ISOLATING OR SEPARATING AN ANIMAL CELL OR COMPOSITION THEREOF; PROCESS OF PREPARING A COMPOSITION CONTAINING AN ANIMAL CELL; CULTURE MEDIA THEREFORE

Examiners

Primary: Campell, Bruce R.
Assistant: Hill, Myron G.

Attorney, Agent or Firm

Foreign Patent References

  • 0 411 678 EP 02/01/1991
  • 0 185 573 EP 06/01/1995
  • 0 833 934 EP 04/01/1998
  • WO 93/03163 WO 02/01/1993
  • WO 95/05465 WO 02/01/1995
  • WO 95/29994 WO 11/01/1995
  • WO 97/00326 WO 01/01/1997
  • WO97/00326 WO 10/01/1997
  • WO 98/18926 WO 05/01/1998
  • WO 98/39411 WO 09/01/1998
  • WO 98/44141 WO 10/01/1998
  • WO 99/05268 WO 02/01/1999
  • WO 99/24068 WO 05/01/1999
  • WO 00/61164 WO 10/01/2000
  • WO 00/63403 WO 10/01/2000
  • WO 01/38362 WO 05/01/2001
  • WO 02/053580 WO 07/01/2002
  • WO 03/038100 WO 05/01/2003
  • WO 03/048197 WO 06/01/2003
  • WO 03/048348 WO 06/01/2003
  • WO 03/051927 WO 06/01/2003
  • WO 2004/003176 WO 01/01/2004
  • WO 2004/099396 WO 11/01/2004

International Class

C12N 7/00

Abstract

Novel means and methods are provided for the production of mammalian viruses comprising, infecting a culture of immortalized human cells with the virus, incubating the culture infected with virus to propagate the virus under conditions that permit growth of the virus, and to form a virus-containing medium, and removing the virus-containing medium. The viruses can be harvested and be used for the production of vaccines. Advantages are that human cells of the present invention can be cultured under defined serum free conditions, and the cells show improved capability for propagating virus. In particular, methods are provided for producing, in cultured human cells, influenza virus and vaccines derived thereof. This method eliminates the necessity to use whole chicken embryos for the production of influenza vaccines. The method provides also for the continuous or batchwise removal of culture media. As such, the present invention allows the large-scale, continuous production of viruses to a high titer.

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