细胞毒性T细胞
CD3型
T细胞
细胞培养
Jurkat细胞
细胞毒性
整合素
分子生物学
癌症研究
细胞生物学
抗原
化学
细胞
生物
CD8型
免疫学
体外
免疫系统
生物化学
遗传学
作者
Kwanpirom Suwanchiwasiri,Nattaporn Phanthaphol,Chalermchai Somboonpatarakun,Pornpimon Yuti,Jatuporn Sujjitjoon,Piriya Luangwattananun,John Maher,Pa‐thai Yenchitsomanus,Mutita Junking
标识
DOI:10.1016/j.biopha.2024.116718
摘要
Advanced cholangiocarcinoma (CCA) presents a clinical challenge due to limited treatment options, necessitating exploration of innovative therapeutic approaches. Bispecific T cell engager (BTE)-armed T cell therapy shows promise in hematological and solid malignancies, offering potential advantages in safety over continuous BTE infusion. In this context, we developed a novel BTE, targeting CD3 on T cells and integrin αvβ6, an antigen elevated in various epithelial malignancies, on cancer cells. The novel BTE was generated by fusing an integrin αvβ6-binding peptide (A20) to an anti-CD3 (OKT3) single-chain variable fragment (scFv) through a G
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