Arming CAR-T cells with cytokines and more: Innovations in the fourth-generation CAR-T development

嵌合抗原受体 细胞因子 免疫学 生物 抗原 受体 免疫系统 免疫疗法 癌症研究 遗传学
作者
Lin Tang,Sheng Pan,Xuyong Wei,Xiao Xu,Qiang Wei
出处
期刊:Molecular Therapy [Elsevier]
卷期号:31 (11): 3146-3162 被引量:15
标识
DOI:10.1016/j.ymthe.2023.09.021
摘要

Chimeric antigen receptor T cells (CAR-T) therapy has shown great potential in tumor treatment. However, many factors impair the efficacy of CAR-T therapy, such as antigenic heterogeneity and loss, limited potency and persistence, poor infiltration capacity, and a suppressive tumor microenvironment. To overcome these obstacles, recent studies have reported a new generation of CAR-T cells expressing cytokines called armored CAR-T, TRUCK-T, or the fourth-generation CAR-T. Here we summarize the strategies of arming CAR-T cells with natural or synthetic cytokine signals to enhance their anti-tumor capacity. Moreover, we summarize the advances in CAR-T cells expressing non-cytokine proteins, such as membrane receptors, antibodies, enzymes, co-stimulatory molecules, and transcriptional factors. Furthermore, we discuss several prospective strategies for armored CAR-T therapy development. Altogether, these ideas may provide new insights for the innovations of the next-generation CAR-T therapy. Chimeric antigen receptor T cells (CAR-T) therapy has shown great potential in tumor treatment. However, many factors impair the efficacy of CAR-T therapy, such as antigenic heterogeneity and loss, limited potency and persistence, poor infiltration capacity, and a suppressive tumor microenvironment. To overcome these obstacles, recent studies have reported a new generation of CAR-T cells expressing cytokines called armored CAR-T, TRUCK-T, or the fourth-generation CAR-T. Here we summarize the strategies of arming CAR-T cells with natural or synthetic cytokine signals to enhance their anti-tumor capacity. Moreover, we summarize the advances in CAR-T cells expressing non-cytokine proteins, such as membrane receptors, antibodies, enzymes, co-stimulatory molecules, and transcriptional factors. Furthermore, we discuss several prospective strategies for armored CAR-T therapy development. Altogether, these ideas may provide new insights for the innovations of the next-generation CAR-T therapy.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
大幅提高文件上传限制,最高150M (2024-4-1)

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
虚幻的香彤完成签到,获得积分10
2秒前
科研通AI2S应助猪猪采纳,获得10
2秒前
幸福的小刺猬完成签到 ,获得积分10
3秒前
青黛发布了新的文献求助10
3秒前
思源应助YUU采纳,获得10
4秒前
11完成签到,获得积分10
5秒前
小丸子完成签到 ,获得积分10
5秒前
现代绮玉完成签到,获得积分10
6秒前
烟花应助Lucien采纳,获得10
6秒前
tanghong完成签到,获得积分10
7秒前
7秒前
自由的信仰完成签到,获得积分10
7秒前
衣蝉完成签到 ,获得积分10
8秒前
好旺完成签到,获得积分10
8秒前
小赵完成签到,获得积分10
10秒前
菜心完成签到,获得积分10
10秒前
舒适的石头完成签到,获得积分10
10秒前
秀丽的初柔完成签到,获得积分10
11秒前
邓娅琴完成签到 ,获得积分10
12秒前
ss发布了新的文献求助10
12秒前
CLMY完成签到,获得积分10
12秒前
传奇3应助蛙趣采纳,获得10
12秒前
老肖发布了新的文献求助10
12秒前
mss12138完成签到,获得积分10
13秒前
Grace159完成签到 ,获得积分10
13秒前
猪猪完成签到,获得积分20
13秒前
YUU完成签到,获得积分10
14秒前
暄anbujun完成签到,获得积分10
15秒前
西皮完成签到 ,获得积分10
16秒前
16秒前
亦清完成签到,获得积分10
17秒前
moon完成签到,获得积分10
18秒前
18秒前
舒服的灰狼完成签到 ,获得积分10
18秒前
DDTT完成签到,获得积分10
18秒前
英姑应助猪猪采纳,获得10
18秒前
feilei完成签到,获得积分10
19秒前
19秒前
fxx2021完成签到,获得积分10
20秒前
高分求助中
The Young builders of New china : the visit of the delegation of the WFDY to the Chinese People's Republic 1000
юрские динозавры восточного забайкалья 800
English Wealden Fossils 700
Chen Hansheng: China’s Last Romantic Revolutionary 500
宽禁带半导体紫外光电探测器 388
Case Research: The Case Writing Process 300
Global Geological Record of Lake Basins 300
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 催化作用 物理化学 免疫学 量子力学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 3142849
求助须知:如何正确求助?哪些是违规求助? 2793801
关于积分的说明 7807889
捐赠科研通 2450113
什么是DOI,文献DOI怎么找? 1303653
科研通“疑难数据库(出版商)”最低求助积分说明 627017
版权声明 601350