封锁
CD8型
癌症研究
体内
免疫疗法
细胞毒性T细胞
肿瘤浸润淋巴细胞
医学
癌症免疫疗法
T细胞
抗体
免疫系统
免疫学
药理学
体外
化学
生物
内科学
受体
生物化学
生物技术
作者
Seung Hyuck Jeon,Gihoon You,Junsik Park,Youseung Chung,Kyungjin Park,Hyunjoo Kim,Jaehyoung Jeon,Youngkwang Kim,Woo‐Chan Son,Da Som Jeong,Eui‐Cheol Shin,Jung‐Yun Lee,Dai Hoon Han,Jaeho Jung,Su‐Hyung Park
标识
DOI:10.1158/1078-0432.ccr-23-2864
摘要
To overcome the limited efficacy of immune checkpoint blockade, there is a need to find novel cancer immunotherapeutic strategies for the optimal treatment of cancer. The novel anti-4-1BB×PD-L1 bispecific antibody-ABL503 (also known as TJ-L14B)-was designed to simultaneously target PD-L1 and 4-1BB, and demonstrated strong antitumor T-cell responses without considerable toxicity. Here, we investigated how the combination of ABL503 and anti-PD-1 blockade affected the reinvigoration of exhausted tumor-infiltrating CD8+ T cells (CD8+ TILs) and anti-tumor efficacy.
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