化学
兴奋剂
双特异性抗体
癌症
药品
癌症研究
白细胞介素2
抗体
临床试验
白细胞介素
治疗窗口
重组DNA
细胞因子
免疫疗法
T细胞
药物发现
药物开发
药理学
癌症治疗
临床疗效
医学
免疫学
药代动力学
细胞培养
癌细胞
效力
细胞
药物设计
标识
DOI:10.1021/acs.jmedchem.5c03844
摘要
Interleukin-2 (IL-2) is one of the first FDA-proved drugs in cancer immunotherapy. In the past 20 years, lots of new drug's development based on biased IL-2 agonist to expand the therapeutic window had been studied in preclinical and clinical trials. Unfortunately, most of them failed in different stages of clinical trials. Recently, the bispecific antibody which combined two drug-targets of IL-2 and another T cell agonist showed great efficacy in clinical trials. This viewpoint summarizes the history of novel drug design for recombinant IL-2 variants and concludes the promising drug design of IL-2-based bispecific antibodies according to the target mechanism-of-action (MOA) and preclinical/clinical data.
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