CA2164324A1 - Generation concentration and efficient transfer of vsv-g pseudotyped retroviral vectors - Google Patents

Generation concentration and efficient transfer of vsv-g pseudotyped retroviral vectors

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Publication number
CA2164324A1
CA2164324A1 CA002164324A CA2164324A CA2164324A1 CA 2164324 A1 CA2164324 A1 CA 2164324A1 CA 002164324 A CA002164324 A CA 002164324A CA 2164324 A CA2164324 A CA 2164324A CA 2164324 A1 CA2164324 A1 CA 2164324A1
Authority
CA
Canada
Prior art keywords
vectors
retroviral
cells
present application
cell line
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.)
Granted
Application number
CA002164324A
Other languages
French (fr)
Other versions
CA2164324C (en
Inventor
Jane C. Burns
Jiing-Kuan Yee
Theodore Friedmann
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.)
University of California
Original Assignee
Individual
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
Priority claimed from US08/104,804 external-priority patent/US5512421A/en
Application filed by Individual filed Critical Individual
Publication of CA2164324A1 publication Critical patent/CA2164324A1/en
Application granted granted Critical
Publication of CA2164324C publication Critical patent/CA2164324C/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Abstract

The present application discloses retrovirus-derived vectors in which the retroviral envelope glycoprotein has been replaced by the G
glycoprotein of vesicular stomatitis virus, and the use of these vectors in the transfer of exogenous genes into the cells of a wide variety of non-mammalian organisms. Also disclosed is a method for the generation of retroviral vectors in high titers, wherein a recombinant, stable host cell line is provided which harbors the retroviral vector of interest without envelope protein. High-titer retroviral vector production is initiated by introducing nucleic acid encoding a functional membrane-associated protein into the cell line. The vectors disclosed in the present application can be concentrated by ultracentrifugation to titers greater than 10 9 cfu/ml which are especially useful in human gene therapy trials, and can also infect cells, such as hamster and fish cells, that are ordinarily resistant to infection with vectors containing the retroviral envelope protein.
CA002164324A 1993-06-04 1994-06-03 Generation concentration and efficient transfer of vsv-g pseudotyped retroviral vectors Expired - Lifetime CA2164324C (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US7320993A 1993-06-04 1993-06-04
US08/073,209 1993-06-04
US08/104,804 1993-08-10
US08/104,804 US5512421A (en) 1991-02-19 1993-08-10 Generation, concentration and efficient transfer of VSV-G pseudotyped retroviral vectors
PCT/US1994/006272 WO1994029440A1 (en) 1993-06-04 1994-06-03 Generation, concentration and efficient transfer of vsv-g pseudotyped retroviral vectors

Publications (2)

Publication Number Publication Date
CA2164324A1 true CA2164324A1 (en) 1994-12-22
CA2164324C CA2164324C (en) 2005-12-06

Family

ID=35519634

Family Applications (1)

Application Number Title Priority Date Filing Date
CA002164324A Expired - Lifetime CA2164324C (en) 1993-06-04 1994-06-03 Generation concentration and efficient transfer of vsv-g pseudotyped retroviral vectors

Country Status (1)

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CA (1) CA2164324C (en)

Also Published As

Publication number Publication date
CA2164324C (en) 2005-12-06

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Effective date: 20140603