Abstract
Over the last 15 years various methods for delivering genes into mammalian cells have been developed. A great number of possible therapeutic applications have been envisaged. Medical specialists and the public have followed these recent developments with great interest. It is generally admitted that no attempts to introduce germline genetic alterations should be made. Therefore, this paper will focus on somatic gene therapy, in which genetic modifications are applied to somatic cells of an individual patient. The expected clinical benefit from genetic modification of somatic cells needs to be assessed carefully, and its potential risks have to be taken in consideration. Regardless of the technological strategy chosen by the scientist/physician, nonpropagat in g and nontrans- missive gene transfer delivery systems are mandatory at the present time.
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Schadendorf, D., Dummet, R. (1997). Gene Therapy: A New Perspective for the Treatment of Malignant Melanoma. In: Burg, G., Dummer, R.G. (eds) Strategies for Immunointerventions in Dermatology. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-60752-3_34
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DOI: https://doi.org/10.1007/978-3-642-60752-3_34
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