TY - JOUR
T1 - Mining the microbiota for microbial and metabolite-based immunotherapies
AU - Skelly, Ashwin N.
AU - Sato, Yuko
AU - Kearney, Sean
AU - Honda, Kenya
N1 - Funding Information:
This work was supported by the Japan Agency for Medical Research and Development (AMED) LEAP under grant number JP18gm0010003, the Takeda Science Foundation, the Mitsukoshi Health and Welfare Foundation (K.H.) and Grant-in-Aid for Japan Society for the Promotion of Science (JSPS) Fellows (18F18104) (S.K.).
Publisher Copyright:
© 2019, The Author(s), under exclusive licence to Springer Nature Limited.
PY - 2019/5/1
Y1 - 2019/5/1
N2 - Trillions of microorganisms transit through and reside in the mammalian gastrointestinal tract each day, collectively producing thousands of small molecules and metabolites with local and systemic effects on host physiology. Identifying effector microorganisms that causally affect host phenotype and deciphering the underlying mechanisms have become foci of microbiome research and have begun to enable the development of microbiota-based therapeutics. Two complementary, reductionist approaches have commonly been used: the first starts with an immune phenotype and narrows down the microbiota to identify responsible effector bacteria, while the second starts with bacteria-derived molecules and metabolites and seeks to understand their effects on the host immune system. Together, these strategies provide the basis for the rational design of microbial and metabolite-based therapeutics that target and ameliorate immune deficits in patients.
AB - Trillions of microorganisms transit through and reside in the mammalian gastrointestinal tract each day, collectively producing thousands of small molecules and metabolites with local and systemic effects on host physiology. Identifying effector microorganisms that causally affect host phenotype and deciphering the underlying mechanisms have become foci of microbiome research and have begun to enable the development of microbiota-based therapeutics. Two complementary, reductionist approaches have commonly been used: the first starts with an immune phenotype and narrows down the microbiota to identify responsible effector bacteria, while the second starts with bacteria-derived molecules and metabolites and seeks to understand their effects on the host immune system. Together, these strategies provide the basis for the rational design of microbial and metabolite-based therapeutics that target and ameliorate immune deficits in patients.
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U2 - 10.1038/s41577-019-0144-5
DO - 10.1038/s41577-019-0144-5
M3 - Review article
C2 - 30858494
AN - SCOPUS:85062881986
SN - 1474-1733
VL - 19
SP - 305
EP - 323
JO - Nature Reviews Immunology
JF - Nature Reviews Immunology
IS - 5
ER -