Construction of new retroviral producer cells from adenoviral and retroviral vectors View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

1998-09

AUTHORS

X Lin

ABSTRACT

A combination of adenoviral and retroviral vectors was used to construct second generation packaging cells that deliver marker genes to target cells. A vector based upon Moloney murine leukemia virus (MoMLV) was used to deliver marker genes, and an adenovirus-based delivery system was used to deliver MoMLV structural genes (gag pol and env) to cultured cells. The procedure transformed the cells into new retroviral producer cells, which generate replication-incompetent retroviral particles in the culture supernatant for transferring marker genes to target cells. The titer of the retroviral-containing supernatant generated from the second generation producer cells reached above 10(5) c.f.u./ml, which is comparable to the MoMLV-based producer cell lines currently used in human gene therapy trials. These observations suggest that this new gene transfer scheme is technically feasible. The vector and procedures may be adapted for experimental human gene therapy in which the new producer cells are transplanted into patients for continuous gene transfer. More... »

PAGES

1251

References to SciGraph publications

  • 1991-04-22. Manipulation of Adenovirus Vectors in GENE TRANSFER AND EXPRESSION PROTOCOLS
  • 1975-10. Human serum lyses RNA tumour viruses in NATURE
  • 1990. Virus Isolation and Production in TECHNIQUES IN HIV RESEARCH
  • 1995-03. Gene Therapy Vectors As Drug Delivery Systems in CLINICAL PHARMACOKINETICS
  • 1995. Gene Therapy in Heart Disease in NUTRITION AND BIOTECHNOLOGY IN HEART DISEASE AND CANCER
  • Identifiers

    URI

    http://scigraph.springernature.com/pub.10.1038/sj.gt.3300720

    DOI

    http://dx.doi.org/10.1038/sj.gt.3300720

    DIMENSIONS

    https://app.dimensions.ai/details/publication/pub.1036620991

    PUBMED

    https://www.ncbi.nlm.nih.gov/pubmed/9930327


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