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Gene Therapy Using Adenovirus Vectors

  • Chapter
The Molecular Repertoire of Adenoviruses III

Part of the book series: Current Topics in Microbiology and Immunology ((CT MICROBIOLOGY,volume 199/3))

Abstract

Remarkable progress has been made in the field of gene therapy during the last few years. Genetic as well as acquired diseases such as cancer could potentially be treated by this approach. Among the available vectors for gene transfer, replication-deficient recombinant adenoviruses (Ad) appear attractive. They are easy to manipulate, infect many different types of cells (even nondividing ones), can be prepared at high titers, and, of particular importance, they are capable of direct in vivo introduction of foreign genetic material into the body.

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Authors and Affiliations

  1. Laboratorie de Génétique des Virus Oncogènes, Institut Gustave Roussy, PR2, 39 rue Camille Desmoulins, 94805, Villejuif Cedex, France

    H. Haddada, L. Cordier & M. Perricaudet

Authors
  1. H. Haddada
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  2. L. Cordier
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  3. M. Perricaudet
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Editors and Affiliations

  1. Institut für Genetik, Universität zu Köln, Weyertal 121, 50931, Köln, Germany

    Walter Doerfler  & Petra Böhm  & 

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© 1995 Springer-Verlag Berlin Heidelberg

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Haddada, H., Cordier, L., Perricaudet, M. (1995). Gene Therapy Using Adenovirus Vectors. In: Doerfler, W., Böhm, P. (eds) The Molecular Repertoire of Adenoviruses III. Current Topics in Microbiology and Immunology, vol 199/3. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-79586-2_14

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  • DOI: https://doi.org/10.1007/978-3-642-79586-2_14

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-79588-6

  • Online ISBN: 978-3-642-79586-2

  • eBook Packages: Springer Book Archive

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