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嵌合抗原受体结构与使用不同生物反应器生产临床级 CAR 工程化细胞

英文原题:Chimeric Antigen Receptor Structure and Manufacturing of Clinical Grade CAR Engineered Cells using Different Bioreactors.

查看英文原题

Chimeric Antigen Receptor Structure and Manufacturing of Clinical Grade CAR Engineered Cells using Different Bioreactors.

PubMed 2022/11/07(内容时间) Hematol Oncol Stem Cell Ther

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中文摘要

嵌合抗原受体(CAR)T细胞等适应性细胞治疗(ACT)日益取得成功,显示基因工程改造T细胞在部分血液系统恶性肿瘤中具有重要技术进步和令人瞩目的临床疗效。为克服传统CAR治疗的局限并拓展CAR-T 用于更多恶性肿瘤,有必要开发超越传统结构的新型CAR设计。研究人员已提出多种工程策略,以提高这一疗法的安全性、疗效和适用范围。本文介绍模块化CAR结构及其必需结构域,并总结T细胞内CAR近端信号传导的相关认识。

此外,全球过继细胞治疗需求迅速增长,亟需全自动化制造方法,以大规模生产临床级、高质量的CAR工程化免疫细胞。尽管临床级CAR细胞生产的自动化已取得进展,制造流程仍成本高、需要保持一致性,且包含细胞筛选、活化、转导和体外扩增等多个步骤。在这些复杂环节中,需要评估并优化培养系统,以产生大量功能性细胞。本文列举了可用于临床试验临床级CAR工程化细胞生产的先进全自动和半自动生物反应器平台,但这些平台尚未标准化。系统推动生产自动化、标准化和规模化,有望降低成本并最终使个体化疗法惠及更多患者。本文详细介绍现有CAR工程化T细胞平台,以及未来用于临床级CAR工程化先进治疗药品(ATMP)生产的平台。

展开英文摘要原文

Increasing success of adaptive cell therapy (ACT), such as genetically engineered T cells to express chimeric antigen receptors (CARs) proven to be highly significant technological advancements and impressive clinical outcomes in selected haematological malignancies, with promising efficacy.

The evolution of CAR designs beyond the conventional structures is necessary to address some of the limitations of conventional CAR therapy and to expand the use of CAR T cells to a wider range of malignancies. There are various obstacles with a wide range of engineering strategies in order to improve the safety, efficacy and applicability of this therapeutic modality.

Here we describe details of modular CAR structure with all the necessary domains and what is known about proximal CAR signalling in T cells.

Furthermore, the global need for adoptive cell therapy is expanding very rapidly, and there is an urgent increasing demand for fully automated manufacturing methods that can produce large scale clinical grade high quality CAR engineered immune cells.

Despite the advances in automation for the production of clinical grade CAR engineered cells, the manufacturing process is costly, consistent and involves multiple steps, including selection, activation, transduction, and Ex-Vivo expansion. Among these complex manufacturing phases, the choice of culture system to generate a high number of functional cells needs to be evaluated and optimized.

Here we list the most advance fully automated to semi-automated bioreactor platforms can be used for the production of clinical grade CAR engineered cells for clinical trials but are far from being standardized.

New processing options are available and a systematic effort seeking automation, standardization and the increase of production scale, would certainly help to bring the costs down and ultimately democratise this personalized therapy. In this review, we describe in detail different CAR engineered T cell platforms available and can be used in future for clinical-grade CAR engineered ATMP production.

论文信息

作者
Syed F、El Fakih R、Alahmari AD、Osman Ali AS、Aljurf M
第一作者单位
Stem Cell & Tissue Re-engineering Program (Dpt)-R., King Faisal Specialist Hospital & Research Centre, Riyadh, 11211, Saudi Arabia.Saudi Arabia
通讯作者单位
Oncology Centre, King Faisal Specialist Hospital & Research Centre, Riyadh, 11211, Saudi Arabia.Saudi Arabia
文献类型
综述
期刊
Hematology/oncology and stem cell therapy2022 Nov 7
原文标识
PubMed 36395497 · DOI 10.56875/2589-0646.1048