Enteric helminth-induced type I interferon signaling protects against pulmonary virus infection through interaction with the microbiota.

Details

Serval ID
serval:BIB_CB15D7357546
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Enteric helminth-induced type I interferon signaling protects against pulmonary virus infection through interaction with the microbiota.
Journal
The Journal of allergy and clinical immunology
Author(s)
McFarlane A.J., McSorley H.J., Davidson D.J., Fitch P.M., Errington C., Mackenzie K.J., Gollwitzer E.S., Johnston CJC, MacDonald A.S., Edwards M.R., Harris N.L., Marsland B.J., Maizels R.M., Schwarze J.
ISSN
1097-6825 (Electronic)
ISSN-L
0091-6749
Publication state
Published
Issued date
10/2017
Peer-reviewed
Oui
Volume
140
Number
4
Pages
1068-1078.e6
Language
english
Notes
Publication types: Journal Article
Publication Status: ppublish
Abstract
Helminth parasites have been reported to have beneficial immunomodulatory effects in patients with allergic and autoimmune conditions and detrimental consequences in patients with tuberculosis and some viral infections. Their role in coinfection with respiratory viruses is not clear.
Here we investigated the effects of strictly enteric helminth infection with Heligmosomoides polygyrus on respiratory syncytial virus (RSV) infection in a mouse model.
A murine helminth/RSV coinfection model was developed. Mice were infected by means of oral gavage with 200 stage 3 H polygyrus larvae. Ten days later, mice were infected intranasally with either RSV or UV-inactivated RSV.
H polygyrus-infected mice showed significantly less disease and pulmonary inflammation after RSV infection associated with reduced viral load. Adaptive immune responses, including TH2 responses, were not essential because protection against RSV was maintained in Rag1(-/-) and Il4rα(-/-) mice. Importantly, H polygyrus infection upregulated expression of type I interferons and interferon-stimulated genes in both the duodenum and lung, and its protective effects were lost in both Ifnar1(-/-) and germ-free mice, revealing essential roles for type I interferon signaling and microbiota in H polygyrus-induced protection against RSV.
These data demonstrate that a strictly enteric helminth infection can have remote protective antiviral effects in the lung through induction of a microbiota-dependent type I interferon response.

Keywords
Heligmosomoides polygyrus, Respiratory syncytial virus, helminths, microbiome, type I interferon
Pubmed
Web of science
Create date
21/02/2017 19:22
Last modification date
20/08/2019 16:45
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