Department of Pathology, Yale School of Medicine, New Haven, CT, USA.
Department of Genetics, Yale School of Medicine, New Haven, CT, USA.
Methods Mol Biol. 2020;2097:231-252. doi: 10.1007/978-1-0716-0203-4_15.
Cell-based immunotherapy has achieved preclinical success in certain types of cancer patients, with a few approved cell-based products for clinical use. These achievements revitalized the field of cell engineering/ immunotherapy and brought attention to the opportunities that cell-based immunotherapeutics can offer to patients. On the other hand, obvious indications emphasize the need for a better understanding of the biological mechanisms involved in the immune response. This knowledge may not only ameliorate safety and efficacy, but also determine the possibilities and limitations in use of immune cell engineering for cancer treatment, and facilitate developing novel immunotherapeutic strategies. Recently developed technology based on CRISPR-dCas9 has an immense potential to systematically uncover genetic mechanisms by identifying subsets of essential genes involved in interactions of cancer cells with the immune system. This chapter will present a reliable and reproducible general protocol for the application of genome-wide sgRNA gene-editing tools in the recently established two-cell type co-culture, consisting of immune cells as effectors and cancer cells as targets, utilizing CRISPRi/a-dCas9-based technology.
基于细胞的免疫疗法在某些类型的癌症患者中取得了临床前的成功,已有少数基于细胞的产品获得批准用于临床应用。这些成就使细胞工程/免疫疗法领域重获生机,并使人们关注到细胞免疫疗法可为患者带来的机遇。另一方面,明显的适应证强调了需要更好地了解免疫反应中涉及的生物学机制。这些知识不仅可以改善安全性和疗效,还可以确定免疫细胞工程在癌症治疗中的应用的可能性和局限性,并有助于开发新的免疫治疗策略。基于 CRISPR-dCas9 的新技术具有巨大的潜力,可以通过鉴定与癌细胞与免疫系统相互作用相关的必需基因的亚群,系统地揭示遗传机制。本章将提供一种可靠且可重复的通用方案,用于在最近建立的两细胞型共培养物(由免疫细胞作为效应物和癌细胞作为靶标组成)中应用全基因组 sgRNA 基因编辑工具,该方案利用了基于 CRISPRi/a-dCas9 的技术。