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dc.contributor.authorSanin, DE
dc.contributor.authorPrendergast, CT
dc.contributor.authorBourke, CD
dc.contributor.authorMountford, AP
dc.contributor.editorWynn, TA
dc.date.accessioned2019-02-01T16:21:58Z
dc.date.available2019-02-01T16:21:58Z
dc.date.issued2015-05-14
dc.identifier.citationSanin DE, Prendergast CT, Bourke CD, Mountford AP (2015) Helminth Infection and Commensal Microbiota Drive Early IL-10 Production in the Skin by CD4+ T Cells That Are Functionally Suppressive. PLoS Pathog 11(5): e1004841. https://doi.org/10.1371/journal.ppat.1004841en_US
dc.identifier.issn1932-6203
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/55099
dc.description.abstractThe skin provides an important first line of defence and immunological barrier to invasive pathogens, but immune responses must also be regulated to maintain barrier function and ensure tolerance of skin surface commensal organisms. In schistosomiasis-endemic regions, populations can experience repeated percutaneous exposure to schistosome larvae, however little is known about how repeated exposure to pathogens affects immune regulation in the skin. Here, using a murine model of repeated infection with Schistosoma mansoni larvae, we show that the skin infection site becomes rich in regulatory IL-10, whilst in its absence, inflammation, neutrophil recruitment, and local lymphocyte proliferation is increased. Whilst CD4+ T cells are the primary cellular source of regulatory IL-10, they expressed none of the markers conventionally associated with T regulatory (Treg) cells (i.e. FoxP3, Helios, Nrp1, CD223, or CD49b). Nevertheless, these IL-10+ CD4+ T cells in the skin from repeatedly infected mice are functionally suppressive as they reduced proliferation of responsive CD4+ T cells from the skin draining lymph node. Moreover, the skin of infected Rag-/- mice had impaired IL-10 production and increased neutrophil recruitment. Finally, we show that the mechanism behind IL-10 production by CD4+ T cells in the skin is due to a combination of an initial (day 1) response specific to skin commensal bacteria, and then over the following days schistosome-specific CD4+ T cell responses, which together contribute towards limiting inflammation and tissue damage following schistosome infection. We propose CD4+ T cells in the skin that do not express markers of conventional T regulatory cell populations have a significant role in immune regulation after repeated pathogen exposure and speculate that these cells may also help to maintain skin barrier function in the context of repeated percutaneous insult by other skin pathogensen_US
dc.description.sponsorshipy The Wellcome Trust, grant number: 092745/Z/10/Z.en_US
dc.format.extente1004841 - e1004841
dc.language.isoenen_US
dc.publisherPublic Library of Scienceen_US
dc.relation.ispartofPLOS Pathogens
dc.rightsCreative Commons Attribution
dc.rightsAttribution 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/us/*
dc.subjectHelminth Infectionen_US
dc.subjectimmune responsesen_US
dc.subjectinfectious pathogensen_US
dc.titleHelminth Infection and Commensal Microbiota Drive Early IL-10 Production in the Skin by CD4+ T Cells That Are Functionally Suppressiveen_US
dc.typeArticleen_US
dc.rights.holder2015 Sanin et al.
dc.identifier.doi10.1371/journal.ppat.1004841
pubs.issue5en_US
pubs.notesNot knownen_US
pubs.publication-statusPublisheden_US
pubs.volume11en_US
dcterms.dateAccepted2015-03-30
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US


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