Oelke Mathias, Krueger Christine, Schneck Jonathan P
Department of Pathology & Medicine, The Johns Hopkins School of Medicine, Baltimore, Maryland 21205-2196, USA.
Drugs Today (Barc). 2005 Jan;41(1):13-21. doi: 10.1358/dot.2005.41.1.875775.
Adoptive immunotherapy is an attractive and elegant strategy for treating a variety of life-threatening diseases. Several approaches have been developed to generate antigen-specific CD4+ and CD8+ T cells for adoptive T-cell therapy in cancer and infectious diseases. Currently, many approaches are based on either the use of autologous peptide pulsed dendritic cells as antigen-presenting cells or nonspecific expansion of T cells. Unfortunately, current approaches lack the ability to serve as reproducible and economically viable methods. Several groups are developing new artificial approaches to overcome problems associated with dendritic cells and the nonspecific expansion of T-cell clones in order to make adoptive immunotherapy more feasible and effective. Thus, by increasing the availability of adoptive immunotherapy, we will be able to better determine the efficacy of the approaches in the treatment of a variety of diseases. In this review, we focus on technological advances that will facilitate adoptive immunotherapy. Specifically, we summarize current strategies which are either based on artificial antigen-presenting cells or on T-cell receptor gene transfer.
过继性免疫疗法是一种治疗多种危及生命疾病的有吸引力且精巧的策略。已经开发了几种方法来产生抗原特异性CD4+和CD8+ T细胞,用于癌症和传染病的过继性T细胞治疗。目前,许多方法要么基于使用自体肽脉冲树突状细胞作为抗原呈递细胞,要么基于T细胞的非特异性扩增。不幸的是,目前的方法缺乏作为可重复且经济可行方法的能力。几个研究小组正在开发新的人工方法,以克服与树突状细胞和T细胞克隆非特异性扩增相关的问题,从而使过继性免疫疗法更可行、更有效。因此,通过提高过继性免疫疗法的可用性,我们将能够更好地确定这些方法在治疗多种疾病中的疗效。在这篇综述中,我们关注将促进过继性免疫疗法的技术进展。具体来说,我们总结了目前基于人工抗原呈递细胞或T细胞受体基因转移的策略。