High-capacity adenovirus vector-mediated anti-glioma gene therapy in the presence of systemic antiadenovirus immunity.

Abstract:

:Gene therapy is proposed as a novel therapeutic strategy for treating glioblastoma multiforme (GBM), a devastating brain cancer. In the clinic, antivector immune responses pose formidable challenges. Herein we demonstrate that high-capacity adenovirus vectors (HC-Ads) carrying the conditional cytotoxic gene herpes simplex virus type 1-thymidine kinase (TK) induce tumor regression and long-term survival in an intracranial glioma model, even in the presence of systemic antiadenovirus immunity, as could be encountered in patients. First-generation Ad-TK failed to elicit tumor regression in this model. These results pave the way for implementing HC-Ad-TK-mediated gene therapy as a powerful adjuvant for treating GBM.

journal_name

J Virol

journal_title

Journal of virology

authors

King GD,Muhammad AK,Xiong W,Kroeger KM,Puntel M,Larocque D,Palmer D,Ng P,Lowenstein PR,Castro MG

doi

10.1128/JVI.00232-08

subject

Has Abstract

pub_date

2008-05-01 00:00:00

pages

4680-4

issue

9

eissn

0022-538X

issn

1098-5514

pii

JVI.00232-08

journal_volume

82

pub_type

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