Chimeric antigen receptor structure and manufacturing of clinical grade CAR engineered cells using different bioreactors

嵌合抗原受体 模块化设计 自动化 细胞疗法 计算机科学 基因工程 免疫系统 T细胞 医学 免疫学 干细胞 生物 工程类 机械工程 生物化学 基因 操作系统 遗传学
作者
Farhatullah Syed,Riad El Fakih,Ali D Alahmari,Ahmed S Osman Ali,Mahmoud Aljurf
出处
期刊:Hematology/Oncology and Stem Cell Therapy 卷期号:15 (3): 137-152 被引量:3
标识
DOI:10.56875/2589-0646.1048
摘要

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.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
2秒前
天天快乐应助正正正采纳,获得10
2秒前
2秒前
4秒前
Ethan完成签到,获得积分10
4秒前
sql完成签到,获得积分10
6秒前
6秒前
TDW发布了新的文献求助10
7秒前
QIQ发布了新的文献求助10
7秒前
专一的台灯完成签到,获得积分10
7秒前
qaz完成签到,获得积分10
7秒前
8秒前
10秒前
读研有点小难应助闪闪采纳,获得10
10秒前
10秒前
冷傲雪糕完成签到,获得积分10
10秒前
11秒前
11秒前
赘婿应助dgdsnfds采纳,获得10
11秒前
12秒前
yan发布了新的文献求助10
13秒前
可爱的函函应助Selenge采纳,获得10
13秒前
kokocrl完成签到,获得积分10
14秒前
悸动完成签到 ,获得积分10
14秒前
14秒前
爆米花应助子忧采纳,获得10
15秒前
Liao完成签到,获得积分20
15秒前
15秒前
15秒前
无知发布了新的文献求助10
16秒前
田様应助杨桃采纳,获得10
17秒前
入袍完成签到,获得积分10
18秒前
zhang发布了新的文献求助10
18秒前
xs小仙女完成签到,获得积分20
18秒前
Hello应助乐观的灭龙采纳,获得10
18秒前
18秒前
Liao发布了新的文献求助10
19秒前
汉堡包应助喜羊羊采纳,获得10
19秒前
20秒前
闪闪完成签到,获得积分10
21秒前
高分求助中
Adhesion Science: Principles & Practice 1234
Signals, Systems, and Signal Processing 610
Introduction to Cosmetic Formulation and Technology, 2nd Edition 400
Petrology and Plate Tectonics,2025 400
Burger's Medicinal Chemistry and Drug Discovery 400
A Step-by-Step Guide to Qualitative Data Coding 2nd Edition 400
Programming for Chemical Engineers Using C, C++, and MATLAB 320
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6701317
求助须知:如何正确求助?哪些是违规求助? 8443005
关于积分的说明 18035839
捐赠科研通 5936967
什么是DOI,文献DOI怎么找? 2989024
邀请新用户注册赠送积分活动 1964895
关于科研通互助平台的介绍 1908534