Literature DB >> 2078575

Safety considerations in somatic gene therapy of human disease with retrovirus vectors.

H M Temin1.   

Abstract

Somatic gene therapy of human disease with retrovirus vectors is a new technology with potentially important medical benefits. Although it involves recombinant DNA technologies and modified retroviruses, proper design of the vectors and delivery systems removes most potential foreseen risks. Furthermore, even in the very remote possibility that there is a nontherapeutic biological effect of the treatment, it is unlikely to be a harmful one. Thus, once very safe retrovirus vector-helper cell systems are constructed and in use, safety considerations should not hold up further human trials of retrovirus vectors.

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Year:  1990        PMID: 2078575     DOI: 10.1089/hum.1990.1.2-111

Source DB:  PubMed          Journal:  Hum Gene Ther        ISSN: 1043-0342            Impact factor:   5.695


  24 in total

1.  Psi- vectors: murine leukemia virus-based self-inactivating and self-activating retroviral vectors.

Authors:  K A Delviks; W S Hu; V K Pathak
Journal:  J Virol       Date:  1997-08       Impact factor: 5.103

2.  Human immunodeficiency virus type 1 incorporated with fusion proteins consisting of integrase and the designed polydactyl zinc finger protein E2C can bias integration of viral DNA into a predetermined chromosomal region in human cells.

Authors:  Wenjie Tan; Zheng Dong; Thomas A Wilkinson; Carlos F Barbas; Samson A Chow
Journal:  J Virol       Date:  2006-02       Impact factor: 5.103

3.  Self-deleting retrovirus vectors for gene therapy.

Authors:  A P Russ; C Friedel; M Grez; H von Melchner
Journal:  J Virol       Date:  1996-08       Impact factor: 5.103

Review 4.  Pharmaceutical approach to somatic gene therapy.

Authors:  F D Ledley
Journal:  Pharm Res       Date:  1996-11       Impact factor: 4.200

5.  A conditional self-inactivating retrovirus vector that uses a tetracycline-responsive expression system.

Authors:  J J Hwang; L Li; W F Anderson
Journal:  J Virol       Date:  1997-09       Impact factor: 5.103

6.  Terplex DNA delivery system as a gene carrier.

Authors:  J S Kim; A Maruyama; T Akaike; S W Kim
Journal:  Pharm Res       Date:  1998-01       Impact factor: 4.200

7.  Lentiviral integration preferences in transgenic mice.

Authors:  Shang-Hsun Yang; Pei-Hsun Cheng; Robert T Sullivan; James W Thomas; Anthony W S Chan
Journal:  Genesis       Date:  2008-12       Impact factor: 2.487

8.  In vivo transfer and expression of a human epidermal growth factor gene accelerates wound repair.

Authors:  C Andree; W F Swain; C P Page; M D Macklin; J Slama; D Hatzis; E Eriksson
Journal:  Proc Natl Acad Sci U S A       Date:  1994-12-06       Impact factor: 11.205

9.  Fusion proteins consisting of human immunodeficiency virus type 1 integrase and the designed polydactyl zinc finger protein E2C direct integration of viral DNA into specific sites.

Authors:  Wenjie Tan; Kai Zhu; David J Segal; Carlos F Barbas; Samson A Chow
Journal:  J Virol       Date:  2004-02       Impact factor: 5.103

10.  Comparison of non-viral methods to genetically modify and enrich populations of primary human corneal endothelial cells.

Authors:  Christoph Engler; Clare Kelliher; Karl J Wahlin; Caroline L Speck; Albert S Jun
Journal:  Mol Vis       Date:  2009-04-01       Impact factor: 2.367

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