Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/89004
Title: Interleukin-26 (IL-26) is a novel anti-microbial peptide produced by T cells in response to staphylococcal enterotoxin
Authors: Woetmann, Anders
Alhede, Morten
Dabelsteen, Sally
Bjarnsholt, Thomas
Rybtke, Morten
Nastasi, Claudia
Krejsgaard, Thorbjørn
Andersen, Mads Hald
Bonefeld, Charlotte M.
Geisler, Carsten
Givskov, Michael
Odum, Niels
Keywords: Antimicrobial Peptide
IL-26
Issue Date: 2018
Source: Woetmann, A., Alhede, M., Dabelsteen, S., Bjarnsholt, T., Rybtke, M., Nastasi, C., et al. (2018). Interleukin-26 (IL-26) is a novel anti-microbial peptide produced by T cells in response to staphylococcal enterotoxin. Oncotarget, 9(28), 19481-19489.
Series/Report no.: Oncotarget
Abstract: Anti-microbial peptides are produced at outer and inner surfaces by epithelia and innate immune cells in response to bacterial infection. Staphylococcus aureus is an enterotoxin producing, Gram-positive pathogen, which is a major cause of soft tissue infections and life-threatening bacteremia and sepsis. Here we show that (i) skin T cells in chronic wounds infected with S. aureus express interleukin-26 (IL-26) in situ, (ii) staphylococcal enterotoxins (SE) trigger IL-26 expression in T cell lines and primary skin T cells, and (iii) IL-26 triggers death and inhibits biofilm formation and growth of S. aureus. Thus, we provide novel evidence that IL-26 is an anti-microbial peptide produced by T cells in response to SE. Accordingly, we propose that IL-26 producing T cells take part in the innate immune response to SE producing S. aureus and thus play a novel role in the primary innate immune defense in addition to their classical role in adaptive immunity.
URI: https://hdl.handle.net/10356/89004
http://hdl.handle.net/10220/44765
DOI: http://dx.doi.org/10.18632/oncotarget.24603
Rights: © 2018 The Author(s) (published by Impact Journals). This is an open-access article distributed under the terms of the Creative Commons Attribution License 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SCELSE Journal Articles

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