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用于癌症免疫治疗的工程化自然杀伤细胞

Engineering Natural Killer Cells for Cancer Immunotherapy.

作者信息

Rezvani Katayoun, Rouce Rayne, Liu Enli, Shpall Elizabeth

机构信息

Department of Stem Cell Transplantation and Cellular Therapy, The University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.

Center for Cell and Gene Therapy, Baylor College of Medicine, Houston Methodist Hospital and Texas Children's Hospital, Houston, TX 77030, USA.

出版信息

Mol Ther. 2017 Aug 2;25(8):1769-1781. doi: 10.1016/j.ymthe.2017.06.012. Epub 2017 Jun 28.

Abstract

The past several years have seen tremendous advances in the engineering of immune effector cells as therapy for cancer. While chimeric antigen receptors (CARs) have been used extensively to redirect the specificity of autologous T cells against hematological malignancies with striking clinical results, studies of CAR-modified natural killer (NK) cells have been largely preclinical. In this review, we focus on recent advances in NK cell engineering, particularly on preclinical evidence suggesting that NK cells may be as effective as T cells in recognizing and killing targets after genetic modification. We will discuss strategies to introduce CARs into both primary NK cells and NK cell lines in an effort to provide antigen specificity, the challenges of manufacturing engineered NK cells, and evidence supporting the effectiveness of this approach from preclinical and early-phase clinical studies using CAR-engineered NK cells. CAR-NK cells hold great promise as a novel cellular immunotherapy against refractory malignancies. Notably, NK cells can provide an "off-the-shelf" product, eliminating the need for a personalized and patient-specific product that plagues current CAR-T cell therapies. The ability to more potently direct NK cell-mediated cytotoxicity against refractory tumors through the expression of CAR is likely to contribute to the recent paradigm shift in cancer treatment.

摘要

在过去几年中,作为癌症治疗手段的免疫效应细胞工程取得了巨大进展。嵌合抗原受体(CAR)已被广泛用于重定向自体T细胞针对血液系统恶性肿瘤的特异性,并取得了显著的临床效果,而对CAR修饰的自然杀伤(NK)细胞的研究大多还处于临床前阶段。在本综述中,我们重点关注NK细胞工程的最新进展,特别是临床前证据表明,基因改造后的NK细胞在识别和杀伤靶标方面可能与T细胞一样有效。我们将讨论将CAR引入原代NK细胞和NK细胞系以赋予抗原特异性的策略、制造工程化NK细胞的挑战,以及来自使用CAR工程化NK细胞的临床前和早期临床研究支持该方法有效性的证据。CAR-NK细胞作为一种针对难治性恶性肿瘤的新型细胞免疫疗法具有巨大潜力。值得注意的是,NK细胞可以提供一种“现成可用”的产品,消除了困扰当前CAR-T细胞疗法的个性化和患者特异性产品的需求。通过CAR的表达更有效地引导NK细胞介导的细胞毒性作用于难治性肿瘤的能力,可能会推动癌症治疗领域最近的模式转变。

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