Curtin James F, King Gwendalyn D, Candolfi Marianela, Greeno Remy B, Kroeger Kurt M, Lowenstein Pedro R, Castro Maria G
Gene Therapeutics Research Institute, Cedars-Sinai Medical Center, Research Pavilion, Suite 5090, 8700 Beverly Boulevard, Los Angeles, CA 90048, USA.
Curr Top Med Chem. 2005;5(12):1151-70. doi: 10.2174/156802605774370856.
Glioblastoma (GBM) is a type of intracranial brain tumor, for which there is no cure. In spite of advances in surgery, chemotherapy and radiotherapy, patients die within a year of diagnosis. Therefore, there is a critical need to develop novel therapeutic approaches for this disease. Gene therapy, which is the use of genes or other nucleic acids as drugs, is a powerful new treatment strategy which can be developed to treat GBM. Several treatment modalities are amenable for gene therapy implementation, e.g. conditional cytotoxic approaches, targeted delivery of toxins into the tumor mass, immune stimulatory strategies, and these will all be the focus of this review. Both conditional cytotoxicity and targeted toxin mediated tumor death, are aimed at eliminating an established tumor mass and preventing further growth. Tumors employ several defensive strategies that suppress and inhibit anti-tumor immune responses. A better understanding of the mechanisms involved in eliciting anti-tumor immune responses has identified promising targets for immunotherapy. Immunotherapy is designed to aid the immune system to recognize and destroy tumor cells in order to eliminate the tumor burden. Also, immune-therapeutic strategies have the added advantage that an activated immune system has the capability of recognizing tumor cells at distant sites from the primary tumor, therefore targeting metastasis distant from the primary tumor locale. Pre-clinical models and clinical trials have demonstrated that in spite of their location within the central nervous system (CNS), a tissue described as 'immune privileged', brain tumors can be effectively targeted by the activated immune system following various immunotherapeutic strategies. This review will highlight recent advances in brain tumor immunotherapy, with particular emphasis on advances made using gene therapy strategies, as well as reviewing other novel therapies that can be used in combination with immunotherapy. Another important aspect of implementing gene therapy in the clinical arena is to be able to image the targeting of the therapeutics to the tumors, treatment effectiveness and progression of disease. We have therefore reviewed the most exciting non-invasive, in vivo imaging techniques which can be used in combination with gene therapy to monitor therapeutic efficacy over time.
胶质母细胞瘤(GBM)是一种颅内脑肿瘤,目前尚无治愈方法。尽管在手术、化疗和放疗方面取得了进展,但患者在确诊后一年内死亡。因此,迫切需要为这种疾病开发新的治疗方法。基因治疗是将基因或其他核酸用作药物,是一种可用于治疗GBM的强大新治疗策略。几种治疗方式适用于基因治疗的实施,例如条件性细胞毒性方法、将毒素靶向递送至肿瘤块、免疫刺激策略,这些都将是本综述的重点。条件性细胞毒性和靶向毒素介导的肿瘤死亡,都旨在消除已形成的肿瘤块并防止进一步生长。肿瘤采用多种防御策略来抑制抗肿瘤免疫反应。对引发抗肿瘤免疫反应所涉及机制的更好理解,已经确定了免疫治疗的有前景靶点。免疫治疗旨在帮助免疫系统识别和破坏肿瘤细胞,以消除肿瘤负担。此外,免疫治疗策略还有一个额外的优势,即激活的免疫系统有能力识别远离原发肿瘤部位的肿瘤细胞,因此可以靶向远离原发肿瘤部位的转移灶。临床前模型和临床试验表明,尽管脑肿瘤位于被描述为“免疫特权”的中枢神经系统(CNS)内,但在采用各种免疫治疗策略后,激活的免疫系统可以有效地靶向脑肿瘤。本综述将重点介绍脑肿瘤免疫治疗的最新进展,特别强调使用基因治疗策略取得的进展,以及回顾可与免疫治疗联合使用的其他新疗法。在临床领域实施基因治疗的另一个重要方面是能够对治疗药物在肿瘤中的靶向、治疗效果和疾病进展进行成像。因此,我们综述了最令人兴奋的非侵入性体内成像技术,这些技术可与基因治疗联合使用,以长期监测治疗效果。