研究概要
许多癌症的治疗,尤其是那些仍然难以治疗或在标准治疗后难治的癌症,使用细胞疗法一直具有挑战性。
中文摘要
许多癌症的治疗,尤其是那些仍然难以治疗或在标准治疗后出现难治性的癌症,一直是基于细胞的疗法面临的挑战。尽管作为同种异体疗法相对安全,并且无需抗原致敏即可对癌症产生先天有效性,但自然杀伤(NK)细胞仍需要采用基因操作方法来增强其特异性、持久性和归巢能力。嵌合抗原受体(CAR)和基因编辑NK细胞疗法已成为一种有效的治疗模式,解决了困扰其他细胞类型此类基因疗法的许多问题。工程化NK细胞疗法的早期实例在很大程度上利用了其针对血液系统恶性肿瘤的活性,结合传统构建体结构或通过编辑推测的免疫抑制遗传靶点。随着攻克更复杂实体瘤的动力不断增强,NK特异性构建体和工程方法的复杂性和出现也日益增加。多CAR、与多种基因组编辑技术的组合,以及响应型和感知型CAR已在NK细胞疗法的背景下出现。在此,我们讨论NK细胞疗法的工程方法、该领域的最新进展,以及在通往临床转化道路上阻碍这些前景实现的因素。
展开英文摘要原文
Treatment of many cancers, particularly those that remain difficult to treat or are refractive after standard-of-care therapies, has been challenging with cell-based therapies. Although relatively safe as allogeneic therapies and innately effective against cancers without the need for antigen sensitization, natural killer (NK) cells have necessitated use of genetic manipulation approaches to enhance their specificity, persistence, and homing. Chimeric antigen receptor (CAR) and gene-edited NK cell therapies have emerged as a potent treatment modality, addressing many of the issues that have plagued such gene-based therapies with other cell types. Early examples of engineered NK cell therapies have largely leveraged their activity against hematological malignancies in combination with conventional construct architectures or by editing putative genetic targets of immunosuppression. As the motivation to tackle more complex solid tumors grows, so has the sophistication and emergence of NK-specific constructs and engineering approaches. Multi-CARs, combinations with diverse genome editing technologies, as well as responsive and sensing CARs have appeared in the context of NK cell therapy. Here we discuss engineering approaches for NK cell therapy, the latest developments in the field, and what stands in the way of those promises en route to clinical translation.
论文信息
- 作者
- Wu X、Matosevic S
- 单位
- Department of Industrial and Physical Pharmacy, Purdue University, 575 Stadium Mall Drive RHPH 112E, West Lafayette, IN 47907, USA.United States
- 文献类型
- 综述
- 期刊
- Molecular therapy oncolytics2022 Dec 15