CD19
限制
多路复用
计算生物学
T细胞
细胞
功能(生物学)
嵌合抗原受体
细胞疗法
生物
免疫系统
细胞生物学
计算机科学
免疫学
工程类
遗传学
机械工程
电信
作者
Dragana Slavkovic‐Lukic,Jessica Fioravanti,Azucena Martín-Santos,Edward Han,Jing Zhou,Luca Gattinoni
出处
期刊:Methods in molecular biology
日期:2023-12-10
卷期号:: 135-149
标识
DOI:10.1007/978-1-0716-3593-3_11
摘要
The functional fitness of CAR T cells plays a crucial role in determining their clinical efficacy. Several strategies are being explored to increase cellular fitness, but screening these approaches in vivo is expensive and time-consuming, limiting the number of strategies that can be tested at one time. The presence of polyfunctional CAR T cells has emerged as a critical parameter correlating with clinical responses. However, even sophisticated multiplexed secretomic assays often fail to detect differences in cytokine release due to the functional heterogeneity of CAR T cell products. Here, we describe a highly multiplexed single-cell secretomic assay based on the IsoLight platform to rapidly evaluate the impact of new pharmacologic or gene-engineering approaches aiming at improving CAR T cell function. As a key study, we focus on CD19-specific CAR CD8+ T cells modulated by miR-155 overexpression, but the protocol can be applied to characterize other functional immune cell modulation strategies.
科研通智能强力驱动
Strongly Powered by AbleSci AI