Muul Linda Mesler, Candotti Fabio
Genetics and Molecular Biology Branch, National Human Genome Research Institute, NIH, Bethesda, MD 20892-1451, USA.
Curr Gene Ther. 2007 Oct;7(5):361-8. doi: 10.2174/156652307782151489.
Gene-modified T cells were the first gene therapy tool used in clinical gene transfer trials. After the first applications in immunodeficiency diseases, T cell gene therapy has been extended to HIV infection and cancer. The primary obstacle to successful T cell gene therapy has proven to be the robust immune responses elicited by the gene-modified T cells even in severely immunosuppressed patients. The potent antibody and cytotoxic immune responses have interfered with the expression and persistence of the therapeutic transgene. In this review we will address each of the components of T cell gene therapy -- culture conditions, vector, and transgene -- that have elicited these immune responses and the strategies used to minimize them.
基因修饰的T细胞是临床基因转移试验中使用的首个基因治疗工具。在首次应用于免疫缺陷疾病后,T细胞基因治疗已扩展至HIV感染和癌症领域。事实证明,成功进行T细胞基因治疗的主要障碍是即使在严重免疫抑制的患者中,基因修饰的T细胞也会引发强烈的免疫反应。强效抗体和细胞毒性免疫反应干扰了治疗性转基因的表达和持久性。在本综述中,我们将探讨引发这些免疫反应的T细胞基因治疗的各个组成部分——培养条件、载体和转基因,以及用于将其影响降至最低的策略。