肽聚糖
免疫疗法
癌症免疫疗法
生物
微生物学
先天免疫系统
免疫系统
癌症研究
免疫学
酶
生物化学
作者
Matthew E. Griffin,Juliel Espinosa,Jessica L. Becker,Ji‐Dung Luo,Thomas S. Carroll,Jyoti K. Jha,Gary R. Fanger,Howard C. Hang
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2021-08-26
卷期号:373 (6558): 1040-1046
被引量:213
标识
DOI:10.1126/science.abc9113
摘要
SagA promotes immunotherapy response The gut microbiome can influence the treatment outcome for cancer patients receiving PD-L1 immunotherapy, but the mechanisms underlying favorable responses are unclear. Griffin et al . found that a particular type of bacteria called enterococci enhance anti–PD-L1 immunotherapy in mice (see the Perspective by Ansaldo and Belkaid). The researchers show that enterococci secrete an enzyme called SagA that breaks down components of the bacterial cell wall. This process results in the release of muramyl peptide fragments, which in turn act as stimulatory molecules to promote signaling of the innate immune sensor protein NOD2 and improved immunotherapy responses. —PNK
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