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利用基于 CRISPR 的技术提高癌症免疫疗法。

Improving Cancer Immunotherapy with CRISPR-Based Technology.

机构信息

College of Life and Health Sciences, Northeastern University, Shenyang, 110819, P. R. China.

Key Laboratory of Data Analytics and Optimization for Smart Industry (Northeastern University), Ministry of Education, Shenyang, 110819, P. R. China.

出版信息

Adv Biosyst. 2020 Nov;4(11):e1900253. doi: 10.1002/adbi.201900253. Epub 2020 Feb 19.

DOI:10.1002/adbi.201900253
PMID:33245213
Abstract

The rapidly evolving field of immunotherapy has attracted great attention in the field of cancer research and already revolutionized the clinical practice standard for treating cancer. Genetically engineered T cells expressing either T cell receptors or chimeric antigen receptors represent novel treatment modalities and are considered powerful weapons to fight cancer. The immune checkpoint blockade, which harnesses the negative control signaling behind the anti-tumor immune response with therapeutic antibodies by blocking cytotoxic T lymphocyte-associated protein 4 or the programmed cell death 1 pathways are another mainstream direction for cancer immunotherapy. In addition to cytotoxic T cells, other immune cell types such as nature killer cells and macrophages also possess the ability to eradicate cancer cells, which may serve as the basis to develop novel cancer immunotherapies. The advent of cutting-edge genome editing technology, especially clustered regularly interspaced palindromic repeats (CRISPR)-based tools, has greatly expedited many biomedical research areas, including cancer immunology and immunotherapy. In this review, the contribution of current CRISPR techniques to basic and translational cancer immunology research is discussed, and the future for cancer immunotherapy in the age of CRISPR is predicted.

摘要

免疫疗法是一个快速发展的领域,在癌症研究领域引起了极大关注,已经彻底改变了癌症治疗的临床实践标准。表达嵌合抗原受体或 T 细胞受体的基因工程 T 细胞代表了新的治疗方式,被认为是对抗癌症的有力武器。免疫检查点阻断利用治疗性抗体阻断细胞毒性 T 淋巴细胞相关蛋白 4 或程序性细胞死亡 1 途径的抗肿瘤免疫反应背后的负调控信号,是癌症免疫治疗的另一个主流方向。除了细胞毒性 T 细胞,其他免疫细胞类型,如自然杀伤细胞和巨噬细胞,也具有消灭癌细胞的能力,这可能为开发新的癌症免疫疗法提供依据。前沿的基因组编辑技术,特别是基于成簇规律间隔短回文重复序列(CRISPR)的工具的出现,极大地推动了许多包括癌症免疫学和免疫治疗在内的生物医学研究领域的发展。在本文中,我们探讨了当前 CRISPR 技术对基础和转化癌症免疫学研究的贡献,并对 CRISPR 时代癌症免疫治疗的未来进行了预测。

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