封锁
内吞作用
细胞溶解
免疫
癌症研究
细胞生物学
免疫检查点
免疫学
生物
免疫系统
细胞毒性
受体
遗传学
体外
作者
Elham Ben Saad,Andres Oroya,Nikhil Ponnoor Anto,Meriem Bachais,Christopher E. Rudd
出处
期刊:Cell Reports
[Elsevier]
日期:2024-10-30
卷期号:43 (11): 114907-114907
标识
DOI:10.1016/j.celrep.2024.114907
摘要
PD-1 immune checkpoint blockade (ICB) is a key cancer treatment. While blocking PD-1 binding to ligand is known, the role of internalization in enhancing ICB efficacy is less explored. Our study reveals that PD-1 internalization helps unlock ICB's full potential in cancer immunotherapy. Anti-PD-1 induces 50%-60% surface PD-1 internalization from human and mouse cells, leaving low to intermediate levels of resistant receptors. Complexes then appear in early and late endosomes. Both CD4 and CD8 T cells, especially CD8
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