医学
不利影响
T细胞
模态(人机交互)
药品
细胞毒性T细胞
免疫疗法
抗原
灵活性(工程)
基因组编辑
嵌合抗原受体
免疫学
细胞
癌症研究
自身免疫性疾病
临床实习
肿瘤科
生物信息学
临床试验
重症监护医学
内科学
多样性(控制论)
包装说明书
淋巴细胞活化
治疗方法
计算生物学
精密医学
医学物理学
治疗方式
药理学
作者
P A Baeuerle,Karsten Sauer,R. Grieshaber-Bouyer,J.S. Michaelson
摘要
T cell engagers (TCEs) are antibody-based constructs designed to transiently reprogram cytotoxic T lymphocytes for target cell elimination by simultaneously binding the T cell receptor and a specific surface antigen on the target cell. Over the past 12 years, 10 TCEs were approved by the US Food and Drug Administration, and an additional two by the European Medicines Agency. Nine TCEs treat hematologic malignancies, and three target solid tumors. Over 150 TCEs are being investigated in clinical trials, recently also in autoimmune diseases. Here, we discuss the learnings from the 12 approved TCEs. A surprising variety of molecular designs and biochemical characteristics appear suitable for approval. On the clinical side, we review targets, indications, dosing, schedules, side effects, mitigation strategies for adverse events, and efficacy. High flexibility in design and choice of target, scalability, high response rates as a monotherapy in hematologic malignancies, and emerging efficacy against solid tumors and in autoimmune diseases make TCEs an attractive therapeutic modality.
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