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通过创新实现的进化作为改善 TCR-T 疗法的驱动力

英文原题:Evolution by innovation as a driving force to improve TCR-T therapies.

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Evolution by innovation as a driving force to improve TCR-T therapies.

PubMed 2023/09/21(内容时间) Front Oncol Q2 · IF 3.4(JCR 2025)

研究概要

过继细胞疗法通过基于科学的创新不断演进。

中文摘要

过继细胞疗法通过基于科学的创新不断演进。本文介绍TCR-T疗法领域的专门创新,并将其整合进TCR-T疗法端到端开发平台,以解决关键未满足需求和治疗挑战,包括筛选靶抗原及合适T细胞受体、开发兼具持久疗效和安全性的TCR-T疗法,以及高效、可规模化生产实体瘤患者个体化TCR-T产品。TCR-T疗法开发采用多种可组合创新技术,并按照系统、递进的方式实施。一类技术用于改进产品,使TCR-T疗法更安全、更具特异性且疗效更佳;另一类技术用于优化开发流程,以更快速、更高质量、更高效地完成发现和开发。各模块均在免疫学领域通用基础技术上叠加创新。积极采用“以创新推动演进”的策略,有助于实现开发同类最佳TCR-T疗法、治疗实体瘤患者的总体目标。

展开英文摘要原文

Adoptive cell therapies continually evolve through science-based innovation. Specialized innovations for TCR-T therapies are described here that are embedded in an End-to-End Platform for TCR-T Therapy Development which aims to provide solutions for key unmet patient needs by addressing challenges of TCR-T therapy, including selection of target antigens and suitable T cell receptors, generation of TCR-T therapies that provide long term, durable efficacy and safety and development of efficient and scalable production of patient-specific (personalized) TCR-T therapy for solid tumors. Multiple, combinable, innovative technologies are used in a systematic and sequential manner in the development of TCR-T therapies. One group of technologies encompasses product enhancements that enable TCR-T therapies to be safer, more specific and more effective. The second group of technologies addresses development optimization that supports discovery and development processes for TCR-T therapies to be performed more quickly, with higher quality and greater efficiency. Each module incorporates innovations layered onto basic technologies common to the field of immunology. An active approach of "evolution by innovation" supports the overall goal to develop best-in-class TCR-T therapies for treatment of patients with solid cancer.

论文信息

作者
Schendel DJ
单位
Medigene Immunotherapies GmbH, Planegg, Germany.Germany
文献类型
综述
期刊
Frontiers in oncology2023
原文标识
PubMed 37810959 · DOI 10.3389/fonc.2023.1216829