Blinatumoab公司
双特异性抗体
抗体
医学
计算生物学
计算机科学
免疫学
CD19
单克隆抗体
生物
作者
Gaowei Fan,Zujian Wang,Min Hao,Jinming Li
标识
DOI:10.1186/s13045-015-0227-0
摘要
Bispecific antibodies (BsAbs) recognize two different epitopes. This dual specificity opens up a wide range of applications, including redirecting T cells to tumor cells, blocking two different signaling pathways simultaneously, dual targeting of different disease mediators, and delivering payloads to targeted sites. The approval of catumaxomab (anti-EpCAM and anti-CD3) and blinatumomab (anti-CD19 and anti-CD3) has become a major milestone in the development of bsAbs. Currently, more than 60 different bsAb formats exist, some of them making their way into the clinical pipeline. This review summarizes diverse formats of bsAbs and their clinical applications and sheds light on strategies to optimize the design of bsAbs.
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