Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/79613
Citations
Scopus Web of Science® Altmetric
?
?
Full metadata record
DC FieldValueLanguage
dc.contributor.authorFung, K.-
dc.contributor.authorMangan, N.-
dc.contributor.authorCumming, H.-
dc.contributor.authorHorvat, J.-
dc.contributor.authorMayall, J.-
dc.contributor.authorStifter, S.-
dc.contributor.authorDe Weerd, N.-
dc.contributor.authorRoisman, L.-
dc.contributor.authorRossjohn, J.-
dc.contributor.authorRobertson, S.-
dc.contributor.authorSchjenken, J.-
dc.contributor.authorParker, B.-
dc.contributor.authorGargett, C.-
dc.contributor.authorNguyen, H.-
dc.contributor.authorCarr, D.-
dc.contributor.authorHansbro, P.-
dc.contributor.authorHertzog, P.-
dc.date.issued2013-
dc.identifier.citationScience, 2013; 339(6123):1088-1092-
dc.identifier.issn0036-8075-
dc.identifier.issn1095-9203-
dc.identifier.urihttp://hdl.handle.net/2440/79613-
dc.description.abstractThe innate immune system senses pathogens through pattern-recognition receptors (PRRs) that signal to induce effector cytokines, such as type I interferons (IFNs). We characterized IFN-ε as a type I IFN because it signaled via the Ifnar1 and Ifnar2 receptors to induce IFN-regulated genes. In contrast to other type I IFNs, IFN-ε was not induced by known PRR pathways; instead, IFN-ε was constitutively expressed by epithelial cells of the female reproductive tract (FRT) and was hormonally regulated. Ifn-ε–deficient mice had increased susceptibility to infection of the FRT by the common sexually transmitted infections (STIs) herpes simplex virus 2 and Chlamydia muridarum. Thus, IFN-ε is a potent antipathogen and immunoregulatory cytokine that may be important in combating STIs that represent a major global health and socioeconomic burden.-
dc.description.statementofresponsibilityKa Yee Fung, Niamh E. Mangan, Helen Cumming, Jay C. Horvat, Jemma R. Mayall, Sebastian A. Stifter, Nicole De Weerd, Laila C. Roisman, Jamie Rossjohn, Sarah A. Robertson, John E. Schjenken, Belinda Parker, Caroline E. Gargett, Hong P. T. Nguyen, Daniel J. Carr, Philip M. Hansbro, Paul J. Hertzog-
dc.language.isoen-
dc.publisherAmer Assoc Advancement Science-
dc.rightsCopyright status unknown-
dc.subjectUterus-
dc.subjectVagina-
dc.subjectCell Line-
dc.subjectAnimals-
dc.subjectMice, Inbred C57BL-
dc.subjectHumans-
dc.subjectMice-
dc.subjectChlamydia muridarum-
dc.subjectHerpesvirus 2, Human-
dc.subjectChlamydia Infections-
dc.subjectHerpes Genitalis-
dc.subjectInterferons-
dc.subjectOligodeoxyribonucleotides-
dc.subjectPoly dA-dT-
dc.subjectPoly I-C-
dc.subjectEstrogens-
dc.subjectLigands-
dc.subjectFemale-
dc.subjectToll-Like Receptors-
dc.subjectHEK293 Cells-
dc.titleInterferon-ε protects the female reproductive tract from viral and bacterial infection-
dc.title.alternativeInterferon-epsilon protects the female reproductive tract from viral and bacterial infection-
dc.typeJournal article-
dc.identifier.doi10.1126/science.1233321-
dc.relation.grantARC-
pubs.publication-statusPublished-
dc.identifier.orcidRobertson, S. [0000-0002-9967-0084]-
dc.identifier.orcidSchjenken, J. [0000-0001-6293-6160]-
Appears in Collections:Aurora harvest
Obstetrics and Gynaecology publications

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.