Enterococcus peptidoglycan remodeling promotes checkpoint inhibitor cancer immunotherapy
Author(s) -
Matthew E. Griffin,
Juliel Espinosa,
Jessica L. Becker,
JiDung Luo,
Thomas S. Carroll,
Jyoti K. Jha,
Gary R. Fanger,
Howard C. Hang
Publication year - 2021
Publication title -
science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 12.556
H-Index - 1186
eISSN - 1095-9203
pISSN - 0036-8075
DOI - 10.1126/science.abc9113
Subject(s) - peptidoglycan , immunotherapy , cancer immunotherapy , biology , microbiology and biotechnology , immune system , enterococcus faecalis , immunology , bacteria , escherichia coli , gene , biochemistry , genetics
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. Griffinet 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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