Source:http://linkedlifedata.com/resource/pubmed/id/19890042
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rdf:type | |
lifeskim:mentions |
umls-concept:C0027950,
umls-concept:C0039194,
umls-concept:C0127400,
umls-concept:C0205265,
umls-concept:C0205296,
umls-concept:C0205390,
umls-concept:C0384648,
umls-concept:C0458827,
umls-concept:C0851285,
umls-concept:C0871261,
umls-concept:C1555582,
umls-concept:C1704632,
umls-concept:C1706817,
umls-concept:C2911692
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pubmed:issue |
11
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pubmed:dateCreated |
2009-11-20
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pubmed:abstractText |
Effector Th17 cells are a major source of IL-17, a critical inflammatory cytokine in autoimmune diseases and in host defenses during bacterial infections. Recently, splenic lymphoid tissue inducer-like cells have been reported to be a source of T cell independent IL-17. In this study, we report that the immune system contains a unique set of natural occurring IL-17 producing cell, "natural" Th17 (nTh17), which are a memory-like T cell subset. The nTh17 cells can develop in the absence of the IL-6/STAT3 signaling axis required by inducible Th17 cells. The nTh17 cell population is distinct from conventional inducible Th17 cells, since nTh17 cells express substantial amounts of IL-17A (IL-17), but not IL-17F, under the control of the master regulator, RORgammat. The nTh17 cells simultaneously produce IFN-gamma. DO11.10 transgenic mice with a Rag(-/-) background (DO11.10 Rag(-/-)) lack nTh17 cells, and, following intranasal administration of OVA, IL-17-dependent neutrophil infiltration occurs in DO11.10 transgenic mice, but not in DO11.10 Rag(-/-) mice. The impaired neutrophil-dependent airway response is restored by adaptive transfer of nTh17 cells into DO11.10 Rag(-/-) mice. These results demonstrate that a novel T cell subset, nTh17, facilitates the early phase of Ag-induced airway responses and host defenses against pathogen invasion before the establishment of acquired immunity.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
AIM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
1550-6606
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:day |
1
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pubmed:volume |
183
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
7523-30
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pubmed:meshHeading |
pubmed-meshheading:19890042-Animals,
pubmed-meshheading:19890042-Bronchoalveolar Lavage,
pubmed-meshheading:19890042-CD4-Positive T-Lymphocytes,
pubmed-meshheading:19890042-Cell Lineage,
pubmed-meshheading:19890042-Cytokines,
pubmed-meshheading:19890042-Enzyme-Linked Immunosorbent Assay,
pubmed-meshheading:19890042-Flow Cytometry,
pubmed-meshheading:19890042-Immunologic Memory,
pubmed-meshheading:19890042-Interferon-gamma,
pubmed-meshheading:19890042-Interleukin-17,
pubmed-meshheading:19890042-Mice,
pubmed-meshheading:19890042-Mice, Transgenic,
pubmed-meshheading:19890042-Neutrophil Infiltration,
pubmed-meshheading:19890042-Neutrophils,
pubmed-meshheading:19890042-Ovalbumin,
pubmed-meshheading:19890042-Pneumonia,
pubmed-meshheading:19890042-T-Lymphocyte Subsets
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pubmed:year |
2009
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pubmed:articleTitle |
Natural occurring IL-17 producing T cells regulate the initial phase of neutrophil mediated airway responses.
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pubmed:affiliation |
Laboratory for Signal Network, Research Center for Allergy and Immunology, RIKEN Yokohama Institute, Tsurumi, Yokohama, Kanagawa, Japan.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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