Modulation of Gut Microbiota: A Novel Paradigm of Enhancing the Efficacy of Programmed Death-1 and Programmed Death Ligand-1 Blockade Therapy

被引:52
|
作者
Wang, Yiming [1 ]
Ma, Rena [1 ]
Liu, Fang [1 ]
Lee, Seul A. [1 ]
Zhang, Li [1 ]
机构
[1] Univ New South Wales, Sch Biotechnol & Biomol Sci, Sydney, NSW, Australia
来源
FRONTIERS IN IMMUNOLOGY | 2018年 / 9卷
关键词
gut microbiota; programmed death 1; programmed death ligand 1; cancer immunotherapy; efficacy; GASTRIC EPITHELIAL-CELLS; NECROSIS-FACTOR-ALPHA; UP-REGULATE PD-L1; MUCOSAL T-CELLS; DENDRITIC CELLS; OPEN-LABEL; B7; FAMILY; INFLAMMATORY CYTOKINES; LACTOBACILLUS-CASEI; INTERFERON-GAMMA;
D O I
10.3389/fimmu.2018.00374
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Blockade of programmed death 1 (PD-1) protein and its ligand programmed death ligand 1 (PD-L1) has been used as cancer immunotherapy in recent years, with the blockade of PD-1 being more widely used than blockade of PD-L1. PD-1 and PD-L1 blockade therapy showed benefits in patients with various types of cancer; however, such beneficial effects were seen only in a subgroup of patients. Improving the efficacy of PD-1 and PD-L1 blockade therapy is clearly needed. In this review, we summarize the recent studies on the effects of gut microbiota on PD-1 and PD-L1 blockade and discuss the new perspectives on improving efficacy of PD-1 and PD-L1 blockade therapy in cancer treatment through modulating gut microbiota. We also discuss the possibility that chronic infections or inflammation may impact on PD-1 and PD-L1 blockade therapy.
引用
收藏
页数:13
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