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IL-27 regulation of innate immunity and control of microbial growth.

作者信息

Povroznik Jessica M, Robinson Cory M

机构信息

Department of Microbiology, Immunology & Cell Biology, West Virginia University School of Medicine, Morgantown, WV 26506, USA.

Vaccine Development Center, West Virginia University Health Sciences Center, Morgantown, WV 26506, USA.

出版信息

Future Sci OA. 2020 Jun 17;6(7):FSO588. doi: 10.2144/fsoa-2020-0032.


DOI:10.2144/fsoa-2020-0032
PMID:32802395
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7421895/
Abstract

IL-27 is a pleiotropic cytokine capable of influencing both innate and adaptive immune responses. With anti- and pro-inflammatory activity, IL-27 exerts its opposing effects in a cell-dependent and infectious context-specific manner. Upon pathogenic stimuli, IL-27 regulates innate immune cells, such as monocytes, dendritic cells, macrophages and neutrophils. Immune responses involving these innate cells that are negatively regulated by IL-27 signaling include inflammatory cytokine production, phagolysosomal acidification following phagocytosis, oxidative burst and autophagy. IL-27 signaling is crucial in maintaining the subtle balance between Th1 and Th2 immunity, in which protective inflammation is upregulated within the early stages of infection and subsequently downregulated once microbial growth is controlled. The immunomodulatory effects of IL-27 provide promising therapeutic targets for multiple disease types.

摘要

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本文引用的文献

[1]
Elevated Levels of Interleukin-27 in Early Life Compromise Protective Immunity in a Mouse Model of Gram-Negative Neonatal Sepsis.

Infect Immun. 2020-2-20

[2]
IL-27, IL-30, and IL-35: A Cytokine Triumvirate in Cancer.

Front Oncol. 2019-10-1

[3]
Murine myeloid-derived suppressor cells are a source of elevated levels of interleukin-27 in early life and compromise control of bacterial infection.

Immunol Cell Biol. 2019-2-8

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Int J Mol Sci. 2018-11-11

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Physiol Rev. 2019-1-1

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Sci Rep. 2018-5-15

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Front Immunol. 2018-4-24

[8]
cIAP1/2-TRAF2-SHP-1-Src-MyD88 Complex Regulates Lipopolysaccharide-Induced IL-27 Production through NF-κB Activation in Human Macrophages.

J Immunol. 2018-1-22

[9]
CXCL9, CXCL10, CXCL11/CXCR3 axis for immune activation - A target for novel cancer therapy.

Cancer Treat Rev. 2018-2

[10]
IL-27 Modulates Chemokine Production in TNF-α -Stimulated Human Oral Epithelial Cells.

Cell Physiol Biochem. 2017

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