人树突状细胞:抗肿瘤免疫治疗中的天然佐剂。

M Di Nicola, A Anichini, R Mortarini, M Bregni, G Parmiani, A M Gianni
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引用次数: 0

摘要

虽然最近在几种肿瘤中发现了t细胞定义的肿瘤抗原,但人类肿瘤细胞被认为是免疫原性差的。因此,人类肿瘤免疫治疗临床方法的发展需要鉴定有效的佐剂。树突状细胞(DC)是一种特殊的抗原呈递细胞(APC)系统,可以用作天然佐剂来引发抗肿瘤免疫反应。为了克服成熟DC在外周血中频率低的问题,已经应用了几种方法通过培养动员的CD34+细胞或单核细胞与细胞因子的组合来体外生成人DC。正如在小鼠模型和人体系统中所显示的那样,在装载多肽或肿瘤裂解物或用重组病毒载体感染后,表达肿瘤抗原的DC能够引发特异性抗肿瘤T细胞并介导肿瘤消退。这些初步结果表明,这种新方法可能会导致有效的抗肿瘤反应,即使是在经过大量预处理的晚期癌症患者中,但需要进一步的临床试验来验证肿瘤抗原负载DC疫苗接种的有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Human dendritic cells: natural adjuvants in antitumor immunotherapy.

Although T-cell-defined tumor antigens have recently been identified in several tumors, human neoplastic cells are considered to be poorly immunogenic. The development of clinical approaches to the immunotherapy of human tumors thus requires the identification of effective adjuvants. Dendritic cells (DC) are a specialized system of antigen-presenting cells (APC) that could be utilized as natural adjuvants to elicit antitumor immune responses. In an attempt to overcome the problem of the low frequency of mature DC in peripheral blood, several methods have been applied for the ex vivo generation of human DC by culturing mobilized CD34+ cells or monocytes with combinations of cytokines. As shown in murine models as well as in the human system, after loading with peptides or tumor lysates or infection with recombinant viral vectors, DC expressing tumor antigens are able to elicit specific antitumor T cells and to mediate tumor regression. These initial results suggest that this new approach may lead to effective antitumor responses even in heavily pretreated patients bearing advanced cancers, but further clinical trials are required to validate the efficacy of vaccination with tumor-antigen-loaded DC.

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