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设计更优:新型CAR工程细胞疗法的前景如何?

Better by design: What to expect from novel CAR-engineered cell therapies?

作者信息

Luginbuehl Vera, Abraham Eytan, Kovar Karin, Flaaten Richard, Müller Antonia M S

机构信息

Novartis Oncology, Cell & Gene Therapy, Novartis Pharma Schweiz AG, Rotkreuz, Switzerland.

Personalized Medicine Lonza Pharma&Biotech, Lonza Ltd., Walkersville, MD, USA.

出版信息

Biotechnol Adv. 2022 Sep;58:107917. doi: 10.1016/j.biotechadv.2022.107917. Epub 2022 Feb 9.

Abstract

Chimeric antigen receptor (CAR) technology, and CAR-T cells in particular, have emerged as a new and powerful tool in cancer immunotherapy since demonstrating efficacy against several hematological malignancies. However, despite encouraging clinical results of CAR-T cell therapy products, a significant proportion of patients do not achieve satisfactory responses, or relapse. In addition, CAR-T cell applications to solid tumors is still limited due to the tumor microenvironment and lack of specifically targetable tumor antigens. All current products on the market, as well as most investigational CAR-T cell therapies, are autologous, using the patient's own peripheral blood mononuclear cells as starting material to manufacture a patient-specific batch. Alternative cell sources are, therefore, under investigation (e.g. allogeneic cells from an at least partially human leukocyte antigen (HLA)-matched healthy donor, universal "third-party" cells from a non-HLA-matched donor, cord blood-derived cells, immortalized cell lines or cells differentiated from induced pluripotent stem cells). However, genetic modifications of CAR-engineered cells, bioprocesses used to expand cells, and improved supply chains are still complex and costly. To overcome drawbacks associated with CAR-T technologies, novel CAR designs have been used to genetically engineer cells derived from alpha beta (αβ) T cells, other immune cells such as natural killer (NK) cells, gamma delta (γδ) T cells, macrophages or dendritic cells. This review endeavours to trigger ideas on the next generation of CAR-engineered cell therapies beyond CAR-T cells and, thus, will enable effective, safe and affordable therapies for clinical management of cancer. To achieve this, we present a multidisciplinary overview, addressing a wide range of critical aspects: CAR design, development and manufacturing technologies, pharmacological concepts and clinical applications of CAR-engineered cell therapies. Each of these fields employs a large number of ground-breaking scientific advances, where coordinated and complex process and product development occur at their interfaces.

摘要

嵌合抗原受体(CAR)技术,尤其是CAR-T细胞,自证明对多种血液系统恶性肿瘤有效以来,已成为癌症免疫治疗中的一种新的强大工具。然而,尽管CAR-T细胞治疗产品的临床结果令人鼓舞,但仍有相当一部分患者未获得满意的反应或复发。此外,由于肿瘤微环境和缺乏可特异性靶向的肿瘤抗原,CAR-T细胞在实体瘤中的应用仍然有限。目前市场上的所有产品以及大多数研究性CAR-T细胞疗法都是自体的,使用患者自身的外周血单核细胞作为起始材料来制造患者特异性批次。因此,正在研究替代细胞来源(例如来自至少部分人类白细胞抗原(HLA)匹配的健康供体的同种异体细胞、来自非HLA匹配供体的通用“第三方”细胞、脐带血来源的细胞、永生化细胞系或从诱导多能干细胞分化而来的细胞)。然而,CAR工程细胞的基因改造、用于扩增细胞的生物工艺以及改进的供应链仍然复杂且成本高昂。为了克服与CAR-T技术相关的缺点,新型CAR设计已被用于对源自αβ T细胞、其他免疫细胞(如自然杀伤(NK)细胞、γδ T细胞、巨噬细胞或树突状细胞)的细胞进行基因工程改造。本综述旨在引发关于CAR-T细胞之外的下一代CAR工程细胞疗法的想法,从而为癌症的临床管理提供有效、安全且负担得起的疗法。为了实现这一目标,我们提供了一个多学科概述,涉及广泛的关键方面:CAR设计、开发和制造技术、CAR工程细胞疗法的药理学概念和临床应用。这些领域中的每一个都采用了大量开创性的科学进展,在它们的交叉点上进行着协调且复杂的工艺和产品开发。

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