ONCOLYTIC HERPES SIMPLEX VIRUS 1 (HSV-1) VECTORS: INCREASING TREATMENT EFFICACY AND RANGE THROUGH STRATEGIC VIRUS DESIGN

被引:10
|
作者
Carson, J. [1 ]
Haddad, D. [1 ,2 ]
Bressman, M. [1 ]
Fong, Y. [1 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Surg, New York, NY 10065 USA
[2] Univ Wurzburg, Inst Biochem, Virchow Ctr Expt Biomed, D-8700 Wurzburg, Germany
关键词
ENHANCED THERAPEUTIC-EFFICACY; NV1020 GENOMIC DELETION; HUMAN PROSTATE-CANCER; VIRAL GENE-THERAPY; TYPE-1 MUTANT HF10; REPLICATION-COMPETENT; BREAST-CANCER; RIBONUCLEOTIDE REDUCTASE; SYSTEMIC DELIVERY; LIVER METASTASES;
D O I
10.1358/dof.2010.035.03.1470166
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Viruses have long been considered potential anticancer treatments. Wild-type viruses have been tested as anticancer agents in clinical trials since the 1960s. The possibility of viral oncolysis as an alternate cancer therapy was transformed by the emergence of modern genetic engineering. The herpes simplex virus (HSV) family offers particular advantages for use as a viral oncolytic. The engineered vectors that make up oncolytic HSVs (oHSVs) have demonstrated remarkable safety in clinical trials, with some evidence of efficacy The past decade has seen a focus on increasing the efficacy of oncolytic vectors by adding exogenous trans genes to enhance tumor destruction. The current paper describes the various strategies for engineering HSV for increased cancer tissue specificity and efficacy. Presented are the rationale, preclinical data and clinical data where available. This is meant to illustrate a basic framework for the development of a novel therapy meant to exploit the viral life cycle for the killing of cancer.
引用
收藏
页码:183 / 195
页数:13
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