恶性黑色素瘤的免疫基因治疗方法。2. 临床前研究和临床策略。

B Bonnekoh, J R Bickenbach, D R Roop
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引用次数: 14

摘要

根据主动或被动免疫原理,用于治疗恶性黑色素瘤的免疫基因治疗方法可分为两大类。主动免疫基因治疗可细分为黑色素瘤细胞疫苗、基于dna的疫苗接种和通过细胞介导或直接转移细胞因子和/或细胞表面信号基因治疗已有肿瘤组织。被动免疫基因治疗采用体外激活和扩增的抗肿瘤效应细胞进行过继治疗,涉及基因转移技术的两个主要应用领域,一是对效应细胞进行基因修饰,二是通过与主动免疫基因治疗相同的方法在体内扩增前效应细胞。综述了相应的临床前研究。过去几年开始的临床研究大多仍在进行中,主要关注治疗的安全性和耐受性,而不是疗效。最近的趋势是探索重组腺病毒和牛痘病毒载体,特别是关于体内基因转移的应用。总体而言,黑色素瘤的免疫基因治疗仍处于高度实验性的发展阶段,但未来可能成为一种安全、有效、实用的辅助治疗方式。
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Immunological gene therapy approaches for malignant melanoma. 2. Preclinical studies and clinical strategies.

Immuno-gene therapy approaches for the treatment of malignant melanoma are categorized into two major subgroups according to an active or passive immunological principle. Active immuno-gene therapy is subdivided into melanoma cell vaccines, DNA-based vaccinations and the treatment of pre-existing tumor tissue by cell-mediated or direct transfer of cytokine and/or cell surface signal genes. Passive immuno-gene therapy, employing an adoptive treatment with in vitro activated and expanded anti-tumor effector cells, involves two major application fields for gene transfer techniques, first the genetic modification of the effector cells, and second the in vivo amplification of pre-effector cells by procedures also used in active immuno-gene therapy. Corresponding preclinical studies are reviewed. The clinical studies inaugurated during the last few years are mostly still ongoing and focus on treatment safety and tolerability rather than efficacy. A recent trend is emerging to explore recombinant adenovirus and vaccinia virus vectors particularly with regard to in vivo gene transfer applications. Overall, immuno-gene therapy of melanoma is still in a highly experimental stage of development but may become a safe, efficacious and practical adjuvant treatment modality in the future.

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