免疫疗法
PD-L1
医学
封锁
免疫检查点
细胞毒性T细胞
癌症免疫疗法
癌症治疗
癌症
靶向治疗
联合疗法
癌症研究
免疫系统
免疫学
肿瘤科
药理学
内科学
生物
受体
体外
生物化学
作者
Junhao Li,Lujia Huang,Huiling Zhou,Yi-ming Shan,Fangmin Chen,Vesa‐Pekka Lehto,Wujun Xu,Liqiang Luo,Haijun Yu
标识
DOI:10.1038/s41401-022-00910-w
摘要
Immunotherapy, in particular immune checkpoint blockade (ICB) therapy targeting the programmed cell death-1 (PD-1)/programmed cell death ligand-1 (PD-L1) axis, has remarkably revolutionized cancer treatment in the clinic. Anti-PD-1/PD-L1 therapy is designed to restore the antitumor response of cytotoxic T cells (CTLs) by blocking the interaction between PD-L1 on tumour cells and PD-1 on CTLs. Nevertheless, current anti-PD-1/PD-L1 therapy suffers from poor therapeutic outcomes in a large variety of solid tumours due to insufficient tumour specificity, severe cytotoxic effects, and the occurrence of immune resistance. In recent years, nanosized drug delivery systems (NDDSs), endowed with highly efficient tumour targeting and versatility for combination therapy, have paved a new avenue for cancer immunotherapy. In this review article, we summarized the recent advances in NDDSs for anti-PD-1/PD-L1 therapy. We then discussed the challenges and further provided perspectives to promote the clinical application of NDDS-based anti-PD-1/PD-L1 therapy.
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