Shah Amish C, Benos Dale, Gillespie G Yancey, Markert James M
Department of Physiology and Biophysics, Division of Neurosurgery, University of Alabama at Birmingham, South Birmingham, Alabama 35294, USA.
J Neurooncol. 2003 Dec;65(3):203-26. doi: 10.1023/b:neon.0000003651.97832.6c.
Gene therapy using viral vectors for the treatment of primary brain tumors has proven to be a promising novel treatment modality. Much effort in the past has been placed in utilizing replication-defective viruses to this end but they have shown many disadvantages. Much recent attention has been focused on the potential of replication-competent viruses to discriminatingly target, replicate within, and destroy tumor cells via oncolysis, leaving adjacent post-mitotic neurons unharmed. The engineered tumor-selective herpes simplex-1 virus (HSV-1) mutants G207 and HSV1716 have completed Phase I investigations in the treatment of recurrent high-grade glioma. The results of these clinical trials are reviewed here. This review also aims to examine the manipulation and development of other viruses for the treatment of malignant glioma, including Newcastle disease virus, reovirus, poliovirus, vaccinia virus, and adenoviruses, in particular the adenovirus mutant ONYX-015.
使用病毒载体进行基因治疗以治疗原发性脑肿瘤已被证明是一种很有前景的新型治疗方式。过去人们为此付出了很多努力来利用复制缺陷型病毒,但它们显示出许多缺点。最近,很多注意力都集中在具有复制能力的病毒通过溶瘤作用选择性靶向、在肿瘤细胞内复制并破坏肿瘤细胞,而使相邻的有丝分裂后神经元不受损害的潜力上。经过基因工程改造的肿瘤选择性单纯疱疹病毒1型(HSV-1)突变体G207和HSV1716已完成治疗复发性高级别胶质瘤的I期研究。本文对这些临床试验结果进行了综述。本综述还旨在研究用于治疗恶性胶质瘤的其他病毒的操控和开发,包括新城疫病毒、呼肠孤病毒、脊髓灰质炎病毒、痘苗病毒和腺病毒,特别是腺病毒突变体ONYX-015。