Cardiff University | Prifysgol Caerdydd ORCA
Online Research @ Cardiff 
WelshClear Cookie - decide language by browser settings

Interleukin-27 is a potential rescue therapy for acute severe colitis through Interleukin-10–Dependent, T-Cell–independent attenuation of colonic mucosal innate immune responses

McLean, Mairi H., Andrews, Caroline, Hanson, Miranda L., Baseler, Walter A., Anver, Miriam R., Senkevitch, Emilee, Staniszewska, Aleksandra K., Smith, Christopher, Davies, Luke C., Hixon, Julie, Li, Wenqeng, Shen, Wei, Steidler, Lothar and Durum, Scott K. 2017. Interleukin-27 is a potential rescue therapy for acute severe colitis through Interleukin-10–Dependent, T-Cell–independent attenuation of colonic mucosal innate immune responses. Inflammatory Bowel Diseases 23 (11) , pp. 1983-1995. 10.1097/MIB.0000000000001274

[img]
Preview
PDF - Accepted Post-Print Version
Download (1MB) | Preview

Abstract

Background: If treatment with intravenous steroids fail, inflammatory bowel disease patients with acute severe colitis face systemic anti–tumor necrosis factor biologic rescue therapy or colectomy. Interleukin (IL)-27 is a cytokine with an immunosuppressive role in adaptive immune responses. However, the IL-27 receptor complex is also expressed on innate immune cells, and there is evidence that IL-27 can impact the function of innate cell subsets, although this particular functionality in vivo is not understood. Our aim was to define the efficacy of IL-27 in acute severe colitis and characterize novel IL-27–driven mechanisms of immunosuppression in the colonic mucosa. Methods: We assessed oral delivery of Lactococcus lactis expressing an IL-27 hyperkine on the innate immune response in vivo in a genetically intact, noninfective, acute murine colitis model induced by intrarectal instillation of 2,4,6-trinitrobenzenesulfonic acid in SJL/J mice. Results: IL-27 attenuates acute severe colitis through the reduction of colonic mucosal neutrophil infiltrate associated with a decreased CXC chemokine gradient. This suppression was T cell independent and IL-10 dependent, initially featuring enhanced mucosal IL-10. IL-27 was associated with a reduction in colonic proinflammatory cytokines and induced a multifocal, strong, positive nuclear expression of phosphorylated STAT-1 in mucosal epithelial cells. Conclusion: We have defined novel mechanisms of IL-27 immunosuppression toward colonic innate immune responses in vivo. Mucosal delivery of IL-27 has translational potential as a novel therapeutic for inflammatory bowel disease, and it is a future mucosal directed rescue therapy in acute severe inflammatory bowel disease.

Item Type: Article
Date Type: Publication
Status: Published
Schools: Medicine
Publisher: Wiley: No OnlineOpen / Lippincott, Williams & Wilkins
ISSN: 1078-0998
Funders: Wellcome Trust
Date of First Compliant Deposit: 12 September 2018
Date of Acceptance: 25 July 2017
Last Modified: 15 Mar 2020 10:23
URI: http://orca-mwe.cf.ac.uk/id/eprint/111838

Citation Data

Cited 7 times in Scopus. View in Scopus. Powered By Scopus® Data

Actions (repository staff only)

Edit Item Edit Item

Downloads

Downloads per month over past year

View more statistics