谷歌浏览器插件
订阅小程序
在清言上使用

Tuning the Ignition of CAR: Optimizing the Affinity of Scfv to Improve CAR-T Therapy.

Zhejiang University & Zhejiang Engineering Laboratory for Stem Cell and Immunotherapy,Huang Yanjie,Liao Chan,Tang Yongmin,Zhou Chun,Gao Xiaofei

Cellular and Molecular Life Sciences(2021)

引用 19|浏览14
暂无评分
摘要
How single-chain variable fragments (scFvs) affect the functions of chimeric antigen receptors (CARs) has not been well studied. Here, the components of CAR with an emphasis on scFv were described, and then several methods to measure scFv affinity were discussed. Next, scFv optimization studies for CD19, CD38, HER2, GD2 or EGFR were overviewed, showing that tuning the affinity of scFv could alleviate the on-target/off-tumor toxicity. The affinities of scFvs for different antigens were also summarized to designate a relatively optimal working range for CAR design. Last, a synthetic biology approach utilizing a low-affinity synthetic Notch (synNotch) receptor to achieve ultrasensitivity of antigen-density discrimination and murine models to assay the on-target/off-tumor toxicity of CARs were highlighted. Thus, this review provides preliminary guidelines of choosing the right scFvs for CARs.
更多
查看译文
关键词
Chimeric antigen receptor,scFv,Affinity,On-target/off-tumor,Adoptive cell therapy,Immunotherapy
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要