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GB660109A - Improvements in or relating to the treatment of allantoic fluid containing a propagated virus together with non-viral proteins to obtain the virus in purified and viable from for use in a vaccine - Google Patents

Improvements in or relating to the treatment of allantoic fluid containing a propagated virus together with non-viral proteins to obtain the virus in purified and viable from for use in a vaccine

Info

Publication number
GB660109A
GB660109A GB26374/47A GB2637447A GB660109A GB 660109 A GB660109 A GB 660109A GB 26374/47 A GB26374/47 A GB 26374/47A GB 2637447 A GB2637447 A GB 2637447A GB 660109 A GB660109 A GB 660109A
Authority
GB
United Kingdom
Prior art keywords
virus
purified
fever
viral proteins
volume
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
GB26374/47A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Wyeth Holdings LLC
Original Assignee
American Cyanamid Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by American Cyanamid Co filed Critical American Cyanamid Co
Publication of GB660109A publication Critical patent/GB660109A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N7/00Viruses; Bacteriophages; Compositions thereof; Preparation or purification thereof
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N2760/00MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA ssRNA viruses negative-sense
    • C12N2760/00011Details
    • C12N2760/16011Orthomyxoviridae
    • C12N2760/16111Influenzavirus A, i.e. influenza A virus
    • C12N2760/16151Methods of production or purification of viral material

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Organic Chemistry (AREA)
  • Zoology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Wood Science & Technology (AREA)
  • Medicinal Chemistry (AREA)
  • Biotechnology (AREA)
  • Microbiology (AREA)
  • Biomedical Technology (AREA)
  • Virology (AREA)
  • Biochemistry (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Immunology (AREA)
  • Medicines Containing Antibodies Or Antigens For Use As Internal Diagnostic Agents (AREA)

Abstract

660,109. Vaccines; purified virus. AMERICAN CYANAMID CO. Sept. 30, 1947 [Oct. 1, 1946], No. 26374/47. Class 81 (i). A virus, in purified and viable form for use in a vaccine, is obtained from the allantoic fluid in which it has been propagated by adding 15 to 40 per cent by volume of a water-miscible organic protein-precipitant, e.g. ethyl alcohol, methyl alcohol and acetone, to the fluid which has, or is adjusted to, a pH of 5.0 to 8.0 and ionic strength of 0.005 to 0.5, while maintaining the temperature below 5‹ C., coordinating the volume of precipitant, the pH value, the ionic strength and the temperature to effect selective precipitation of the virus in viable form and separating the precipitated virus from the supernatant fluid containing the non-viral proteins. The precipitated virus is suspended in an aqueous medium, preferably buffered, at a pH 5.0 to 8.0 and at an ionic strength of 0.005 to 0.5, and 15 to 40 per cent by volume of a water-miscible organic protein precipitant added while maintaining the temperature below 5‹ C. The virus precipitate may be removed by low speed centrifugation at a temperature below 5‹ C. Alternatively, the precipitate obtained at the first or subsequent precipitation stages may be suspended in an aqueous medium at the pH and ionic concentration previously stated and the resulting suspension subjected to low speed centrifugation to separate insoluble non-viral proteins and then to high speed centrifugation to separate the virus. The process is particularly applicable to the virus of influenza, equine encephalomyelitis, yellow fever, St. Louis encephalitis, Colorado tick fever, rabies, psittacosis, Rock Mountain spotted fever, epidemic and murine typhus, Q fever, Jap B encephalitis poliomyelitis and Newcastle virus.
GB26374/47A 1946-10-01 1947-09-30 Improvements in or relating to the treatment of allantoic fluid containing a propagated virus together with non-viral proteins to obtain the virus in purified and viable from for use in a vaccine Expired GB660109A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US660109XA 1946-10-01 1946-10-01

Publications (1)

Publication Number Publication Date
GB660109A true GB660109A (en) 1951-10-31

Family

ID=22066680

Family Applications (1)

Application Number Title Priority Date Filing Date
GB26374/47A Expired GB660109A (en) 1946-10-01 1947-09-30 Improvements in or relating to the treatment of allantoic fluid containing a propagated virus together with non-viral proteins to obtain the virus in purified and viable from for use in a vaccine

Country Status (1)

Country Link
GB (1) GB660109A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004113518A1 (en) * 2003-06-20 2004-12-29 Microbix Biosystems Inc. Improvements in virus production
EP1597400A1 (en) * 2003-02-25 2005-11-23 MedImmune Vaccines, Inc. Methods of producing influenza vaccine compositions
US8012736B2 (en) 2002-04-26 2011-09-06 Medimmune, Llc Multi plasmid system for the production of influenza virus
US8093033B2 (en) 2003-12-23 2012-01-10 Medimmune, Llc Multi plasmid system for the production of influenza virus
US8114415B2 (en) 2002-04-26 2012-02-14 Medimmune, Llc Method for producing temperature sensitive influenza A viruses
US8247207B2 (en) 2003-02-25 2012-08-21 Medimmune, Llc Refrigerator-temperature stable influenza vaccine compositions
US8673613B2 (en) 2007-06-18 2014-03-18 Medimmune, Llc Influenza B viruses having alterations in the hemaglutinin polypeptide

Cited By (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8722059B2 (en) 2002-04-26 2014-05-13 Medimmune, Llc Multi plasmid system for the production of influenza virus
US8114415B2 (en) 2002-04-26 2012-02-14 Medimmune, Llc Method for producing temperature sensitive influenza A viruses
US9238825B2 (en) 2002-04-26 2016-01-19 Medimmune, Llc Multi plasmid system for the production of influenza virus
US8012736B2 (en) 2002-04-26 2011-09-06 Medimmune, Llc Multi plasmid system for the production of influenza virus
US8574591B2 (en) 2002-04-26 2013-11-05 Medimmune, Llc Multi plasmid system for the production of influenza virus
US8986705B2 (en) 2003-02-25 2015-03-24 Medimmune, Llc Methods of producing influenza vaccine compositions
US8652822B2 (en) 2003-02-25 2014-02-18 Medimmune, Llc Refrigerator-temperature stable influenza vaccine compositions
EP1597400A4 (en) * 2003-02-25 2007-09-05 Medimmune Vaccines Inc Methods of producing influenza vaccine compositions
US8247207B2 (en) 2003-02-25 2012-08-21 Medimmune, Llc Refrigerator-temperature stable influenza vaccine compositions
EP1597400A1 (en) * 2003-02-25 2005-11-23 MedImmune Vaccines, Inc. Methods of producing influenza vaccine compositions
US7270990B2 (en) 2003-06-20 2007-09-18 Microbix Biosystems, Inc. Virus production
WO2004113518A1 (en) * 2003-06-20 2004-12-29 Microbix Biosystems Inc. Improvements in virus production
US8093033B2 (en) 2003-12-23 2012-01-10 Medimmune, Llc Multi plasmid system for the production of influenza virus
US8409843B2 (en) 2003-12-23 2013-04-02 Medimmune, Llc Multi plasmids system for the production of influenza virus
US9255253B2 (en) 2003-12-23 2016-02-09 Medimmune, Llc Multi plasmid system for the production of influenza virus
US8673613B2 (en) 2007-06-18 2014-03-18 Medimmune, Llc Influenza B viruses having alterations in the hemaglutinin polypeptide
US9068986B2 (en) 2007-06-18 2015-06-30 Medimmune, Llc Influenza B viruses having alterations in the hemagglutinin polypeptide

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