Effectors of the Future: Universal Chimeric Antigen Receptor

IF 1.9 4区 医学 Q3 HEMATOLOGY
Lara Sophie Schlegel, Patrick Schlegel
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Abstract

Background: Cellular therapies leveraging genetically engineered immune effector cells have witnessed a remarkable surge in success, particularly evident in the notable high rates of remission induction and durable remissions observed in a substantial proportion of heavily pretreated patients with refractory B-lineage malignancies. A diverse array of effector cells and therapeutic strategies are now at our disposal, representing the culmination of advancements made over the past 3 decades. The swift pace of development in modern genetic diagnostics, the emergence of spatial proteomics, and the expanding capabilities and precision of computational sciences have profoundly enriched our comprehension of tumor biology and the intricate workings of our immune system. Empowered by advancements in synthetic biology and genome editing, we can expedite the development of next-generation immune effector cells tailored for clinical applications, balancing safety with efficacy. Summary: Universal adapter chimeric antigen receptor (CAR) technologies present the most straightforward solution to tackle antigen heterogeneity and antigen evasion mechanisms employed by tumors. Moreover, due to the decoupling of antigen recognition and signaling in adapter CAR technologies, additional effector functions can safely enhance anticancer activity and most importantly, synergistic combination of patient-specific cellular products with off-the-shelf manufactured antibodies promise increased cost-efficiency. The pivotal collaboration between clinical trial units and regulatory institutions holds the key to surmounting contemporary challenges in trial design, potentially paving the way for the exploration of patient-individualized therapies. Key Messages: In this review, we elaborate on the concept of antibody-dependent cellular cytotoxicity mediated by universal adapter CARs and delineate how recent strides in CAR engineering have the potential to furnish a versatile cellular platform, ushering in an era of cancer-adapted, multitargeted immunotherapies employing universal CAR effector cells.
未来的效应器:通用嵌合抗原受体
背景:利用基因工程免疫效应细胞的细胞疗法取得了显著的成功,特别是在相当一部分接受过大量预处理的难治性B系恶性肿瘤患者中观察到的高缓解诱导率和持久缓解率。我们现在可以使用多种效应细胞和治疗策略,这是过去 30 年来所取得的进步的结晶。现代基因诊断技术的飞速发展、空间蛋白质组学的出现以及计算科学能力和精确度的不断提高,极大地丰富了我们对肿瘤生物学和免疫系统复杂运作的理解。在合成生物学和基因组编辑技术进步的推动下,我们可以加快开发适合临床应用的下一代免疫效应细胞,同时兼顾安全性和有效性。摘要:通用适配器嵌合抗原受体(CAR)技术为解决抗原异质性和肿瘤采用的抗原逃避机制提供了最直接的解决方案。此外,由于适配器嵌合抗原受体(CAR)技术中抗原识别和信号转导的解耦,额外的效应功能可以安全地增强抗癌活性,最重要的是,患者特异性细胞产品与现成抗体的协同组合有望提高成本效益。临床试验单位和监管机构之间的合作至关重要,是克服试验设计中的当代挑战的关键,有可能为探索患者个体化疗法铺平道路。关键信息:在这篇综述中,我们阐述了通用适配CAR介导的抗体依赖性细胞毒性的概念,并描述了CAR工程的最新进展如何有可能提供一个多功能的细胞平台,从而开创一个采用通用CAR效应细胞的癌症适应性多靶点免疫疗法时代。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
4.00
自引率
9.10%
发文量
47
审稿时长
6-12 weeks
期刊介绍: This journal is devoted to all areas of transfusion medicine. These include the quality and security of blood products, therapy with blood components and plasma derivatives, transfusion-related questions in transplantation, stem cell manipulation, therapeutic and diagnostic problems of homeostasis, immuno-hematological investigations, and legal aspects of the production of blood products as well as hemotherapy. Both comprehensive reviews and primary publications that detail the newest work in transfusion medicine and hemotherapy promote the international exchange of knowledge within these disciplines. Consistent with this goal, continuing clinical education is also specifically addressed.
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