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Cited by 224

The DOI matches its Crossref record; 7 of the 7 references it cites were found in a registry or an index.

Microbial Colonization Drives Expansion of IL-1 Receptor 1-Expressing and IL-17-Producing γ/δ T Cells

Open access
Duan, Jinyou, Chung, Hachung, Troy, Erin, Kasper, Dennis L.·2010·Cell Host & Microbe

Abstract

SUMMARY IL-17 cytokine production by the Th17 T-cell subset is regulated by intestinal commmensals. We show microbial colonization also regulates innate IL-17 production. A population of CD62L− γ/δ T cells, in particular a lineage expressing the IL-1 receptor 1 (IL-1R1), can be quickly activated by microbes to produce IL-17. Antibiotic-treatment and monocolonization of mice suggest specific commensals—but not metronidazole-sensitive anaerobes like Bacteroides species—are required for maintaining IL-1R1+ γ/δ T cells. Signaling through the guanine nucleotide exchange factor VAV1 but not through Toll-like receptors or antigen presentation pathways is essential for inducing IL-1R1+ γ/δ T cells. Furthermore, IL-1R1+ γ/δ T cells are a potential source of IL-17 that can be activated by IL-23 and IL-1 in both infectious and noninfectious settings in vitro and in vivo. Thus, commensals orchestrate the expansion of phenotypically distinct γδ T cells and innate immunity is a three-way interaction between host, pathogens and microbiota.

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Metadata

Authors
Duan, J., Chung, H., Troy, E., & Kasper, D. L.
Venue
Cell Host & Microbe
Publisher
Elsevier BV
Published
2010-02
Volume
7
Issue
2
Pages
140-150
ISSN
1931-3128 (ISSN-L)
OpenAlex
W1993187510
Cited by
224
References
7
FWCI
6.91
Type
journal article
Language
en
Open access
bronze

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CoChat. (2026). Citation check: Microbial Colonization Drives Expansion of IL-1 Receptor 1-Expressing and IL-17-Producing γ/δ T Cells. https://app.cochat.ai/papers/10.1016/j.chom.2010.01.005
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Duan, J., Chung, H., Troy, E., & Kasper, D. L. (2010). Microbial Colonization Drives Expansion of IL-1 Receptor 1-Expressing and IL-17-Producing γ/δ T Cells. Cell Host & Microbe. https://doi.org/10.1016/j.chom.2010.01.005

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