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巴西血液学、血液治疗与细胞治疗协会 转基因细胞共识。VII. 嵌合抗原受体(CAR)细胞疗法生产技术的现状与未来。

Associação Brasileira de Hematologia, Hemoterapia e Terapia Celular Consensus on genetically modified cells. VII. Present and future of technologies for production of CAR cell therapies.

作者信息

Ramos Rodrigo Nalio, Picanço-Castro Virginia, Oliveira Theo Gremen M, Mendrone Alfredo, De Santis Gil Cunha, Bonamino Martin Hernan, Rocha Vanderson

机构信息

Laboratório de Investigação Médica em Patogênese e Terapia dirigida em Onco-Imuno-Hematologia, Hospital das Clínicas, Faculdade de Medicina da Universidade de São Paulo (HCFMUSP), São Paulo, SP, Brazil; Instituto D'Or de Ensino e Pesquisa, São Paulo, Brazil.

Fundação Hemocentro de Ribeirão Preto, Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto da Universidade de São Paulo, (HC FMRPUSP) Ribeirão Preto, SP, Brazil.

出版信息

Hematol Transfus Cell Ther. 2021 Nov;43 Suppl 2(Suppl 2):S46-S53. doi: 10.1016/j.htct.2021.09.007.

Abstract

Chimeric Antigen Receptor T (CAR-T) cells are certainly an important therapy for patients with relapsed and/or refractory hematologic malignancies. Currently, there are five CAR-T cell products approved by the FDA but several research groups and/or biopharmaceutical companies are encouraged to develop new products based on CAR cells using T or other cell types. Production of CAR cells requires intensive work from the basic, pre-clinical to translational levels, aiming to overcome technical difficulties and failure in the production. At least five key common steps are needed for the manipulation of T-lymphocytes (or other cells), such as: cell type selection, activation, gene delivery, cell expansion and final product formulation. However, reproducible manufacturing of high-quality clinical-grade CAR cell products is still required to apply this technology to a greater number of patients. This chapter will discuss the present and future development of new CAR designs that are safer and more effective to improve this therapy, achieving more selective killing of malignant cells and less toxicity to be applied in the clinical setting.

摘要

嵌合抗原受体T(CAR-T)细胞无疑是复发和/或难治性血液系统恶性肿瘤患者的一种重要治疗方法。目前,美国食品药品监督管理局(FDA)已批准了五种CAR-T细胞产品,但仍鼓励多个研究团队和/或生物制药公司基于使用T细胞或其他细胞类型的CAR细胞开发新产品。CAR细胞的生产需要从基础、临床前到转化层面开展大量工作,旨在克服生产过程中的技术难题和失败情况。对T淋巴细胞(或其他细胞)进行操作至少需要五个关键的通用步骤,例如:细胞类型选择、激活、基因递送、细胞扩增和最终产品配制。然而,仍需要可重复生产高质量的临床级CAR细胞产品,以便将该技术应用于更多患者。本章将探讨新型CAR设计的当前和未来发展,这些设计更安全、更有效,可改善这种治疗方法,实现对恶性细胞更具选择性的杀伤,并降低在临床应用中的毒性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0ae/8606694/b5133ed6e6ce/gr1.jpg

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