Abakushina Elena V, Popova Liubov I, Zamyatnin Andrey A, Werner Jens, Mikhailovsky Nikolay V, Bazhin Alexandr V
Department for Development and Research in Immunology, LLC "Tecon Medical Devices", 123298 Moscow, Russia.
Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, 119992 Moscow, Russia.
Vaccines (Basel). 2021 Nov 19;9(11):1363. doi: 10.3390/vaccines9111363.
In the last decade, an impressive advance was achieved in adoptive cell therapy (ACT), which has improved therapeutic potential and significant value in promising cancer treatment for patients. The ACT is based on the cell transfer of dendritic cells (DCs) and/or immune effector cells. DCs are often used as vaccine carriers or antigen-presenting cells (APCs) to prime naive T cells ex vivo or in vivo. Cytotoxic T lymphocytes (CTLs) and natural killer (NK) cells are used as major tool effector cells for ACT. Despite the fact that NK cell immunotherapy is highly effective and promising against many cancer types, there are still some limitations, including insignificant infiltration, adverse conditions of the microenvironment, the immunosuppressive cellular populations, and the low cytotoxic activity in solid tumors. To overcome these difficulties, novel methods of NK cell isolation, expansion, and stimulation of cytotoxic activity should be designed. In this review, we discuss the basic characteristics of DC vaccines and NK cells as potential adoptive cell preparations in cancer therapy.
在过去十年中,过继性细胞疗法(ACT)取得了令人瞩目的进展,在有望为患者提供癌症治疗方面具有更高的治疗潜力和重大价值。ACT基于树突状细胞(DC)和/或免疫效应细胞的细胞转移。DC常被用作疫苗载体或抗原呈递细胞(APC),在体外或体内启动初始T细胞。细胞毒性T淋巴细胞(CTL)和自然杀伤(NK)细胞用作ACT的主要工具效应细胞。尽管NK细胞免疫疗法对许多癌症类型具有高效性和前景,但仍存在一些局限性,包括浸润不足、微环境不利条件、免疫抑制细胞群体以及实体瘤中细胞毒性活性较低。为克服这些困难,应设计新型NK细胞分离、扩增和刺激细胞毒性活性的方法。在本综述中,我们讨论了DC疫苗和NK细胞作为癌症治疗中潜在过继性细胞制剂的基本特征。