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Int Immunol. 2017 Feb 1;29(2):71-78. doi: 10.1093/intimm/dxx011.

Dendritic cell expression of the signaling molecule TRAF6 is required for immune tolerance in the lung.

Han D1,2, Walsh MC3, Kim KS1,2, Hong SW1,2, Lee J1,2, Yi J1,2, Rivas G3, Choi Y3, Surh CD1,2,4.

Author information

1
Academy of Immunology and Microbiology, Institute for Basic Science, Pohang 37666, Republic of Korea.
2
Department of Integrative Biosciences and Biotechnology, Pohang University of Science and Technology, Pohang 37666, Republic of Korea.
3
Department of Pathology and Laboratory Medicine, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104, USA.
4
Division of Developmental Immunology, La Jolla Institute for Allergy and Immunology, La Jolla, CA 92037, USA.

Abstract

Immune tolerance in the lung is important for preventing hypersensitivity, such as allergic asthma. Maintenance of tolerance in the lung is established by coordinated activities of poorly understood cellular and molecular mechanisms, including participation of dendritic cells (DCs). We have previously identified DC expression of the signaling molecule TRAF6 as a non-redundant requirement for the maintenance of immune tolerance in the small intestine of mice. Because mucosal tissues share similarities in how they interact with exogenous antigens, we examined the role of DC-expressed TRAF6 in the lung. As with the intestine, we found that the absence TRAF6 expression by DCs led to spontaneous generation of Th2-associated immune responses and increased susceptibility to model antigen-induced asthma. To examine the role of commensal microbiota, mice deficient in TRAF6 in DCs were treated with broad-spectrum antibiotics and/or re-derived on a germ-free (GF) background. Interestingly, we found that antibiotics-treated specific pathogen-free, but not GF, mice showed restored immune tolerance in the absence of DC-expressed TRAF6. We further found that antibiotics mediate microbiota-independent effects on lung T cells to promote immune tolerance in the lung. This work provides both a novel tool for studying immune tolerance in the lung and an advance in our conceptual understanding of potentially common molecular mechanisms of immune tolerance in both the intestine and the lung.

KEYWORDS:

Th2 immunity; antibiotics; asthma; dendritic cell; germ-free

PMID:
28338920
PMCID:
PMC5890897
DOI:
10.1093/intimm/dxx011
[Indexed for MEDLINE]
Free PMC Article

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