Cited by 325Psoriasis: Treatment and PathogenesisT-cell and B-cell ImmunologyIL-33, ST2, and ILC Pathways

γδ T cells: an important source of IL-17

Open access
Roark, Christina L, Simonian, Philip L, Fontenot, Andrew P, Born, Willi K, O’Brien, Rebecca L·2008·Current Opinion in Immunology

Abstract

IL-17 is a cytokine that plays an important role in orchestrating innate immune function. In addition, IL-17 has been shown to exacerbate autoimmune diseases. CD4(+) alphabeta T cells, gammadelta T cells, and NK cells all produce IL-17. Th17 cells are a newly defined alphabeta(+) T cell lineage characterized by IL-17 production. However, gammadelta T cells are often the major source of this cytokine. Their response can be very rapid during bacterial infections and has been shown to be protective, but IL-17-producing gammadelta T cells have also been found to exacerbate collagen-induced arthritis. Interestingly, some gammadelta T cells produce IL-17 in response to IL-23 alone, even in naïve animals, suggesting they are already differentiated and may develop differently than CD4(+) alphabeta Th17 cells.

Integrity signals

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Crossref · 10.1016/j.coi.2008.03.006

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4 of 4 references verified0 citation errors · 0 not checkable

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  • γδ T cells can secrete IFNγ and IL-17 in response to TCR stimulation.

    “Previous reports have demonstrated that γδ T cells can secrete IFNγ and IL-17 in response to TCR stimulation [20]–[22]”

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Authors
Roark, C. L., Simonian, P. L., Fontenot, A. P., Born, W. K., & O’Brien, R. L.
Affiliations
  • National Jewish Health (US)
  • University of Colorado Denver (US)
Venue
Current Opinion in Immunology
Publisher
Elsevier BV
Published
2008-06
Volume
20
Issue
3
Pages
353-357
ISSN
0952-7915 (ISSN-L)
OpenAlex
W2091180924
Cited by
325
References
4
Citations by year
2026: 4 · 2025: 8 · 2024: 4 · 2023: 12 · 2022: 6 · 2021: 9 · 2020: 11 · 2019: 10 · 2018: 9 · 2017: 20 · 2016: 14 · 2015: 18 · 2014: 26 · 2013: 17 · 2012: 30
FWCI
3.11
Type
journal article
Language
en
Open access
Locations
  • Current Opinion in Immunology (publishedVersion)
  • PubMed (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • National Heart, Lung, and Blood Institute (HL062410, HL089766, R01HL065410, 2R01 HL65410, R01HL062410, K08HL089766)
  • National Institute of Allergy and Infectious Diseases (R01AI044920)
Topics
  • Life Sciences › Immunology and Microbiology › Immunology › Psoriasis: Treatment and Pathogenesis
  • Life Sciences › Immunology and Microbiology › Immunology › T-cell and B-cell Immunology
  • Life Sciences › Immunology and Microbiology › Immunology › IL-33, ST2, and ILC Pathways
Keywords
γδ T cells, IL-17, Th17 cells, innate immunity, autoimmune disease, collagen-induced arthritis, IL-23, bacterial infection, T cell differentiation, natural killer cells
MeSH terms
Animals, Autoimmune Diseases, T-Lymphocytes, T-Lymphocyte Subsets, Receptors, Antigen, T-Cell, gamma-delta, Interleukin-17, Mice

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