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Gene therapy progress and prospects: gene therapy for severe combined immunodeficiency.

Authors :
Gaspar, H.B.
Howe, S.
Thrasher, A.J.
Source :
Gene Therapy; Nov2003, Vol. 10 Issue 24, p1999, 6p
Publication Year :
2003

Abstract

Severe combined immunodeficiencies have long been targeted as a group of disorders amenable to gene therapy because of their defined molecular biology and pathophysiology, and the prediction that corrected cells would have profound growth and survival advantage. Recently, several clinical studies have shown that conventional gene transfer technology can produce major beneficial therapeutic effects in these patients, but, as for all cellular and pharmacological treatment approaches, with a finite potential for toxicity.Gene Therapy (2003) 10, 1999-2004. doi:10.1038/sj.gt.3302150 [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09697128
Volume :
10
Issue :
24
Database :
Complementary Index
Journal :
Gene Therapy
Publication Type :
Academic Journal
Accession number :
11140040
Full Text :
https://doi.org/10.1038/sj.gt.3302150