Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/35639
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dc.contributor.authorRyan J.en
dc.contributor.authorFugger L.en
dc.contributor.authorReid H.H.en
dc.contributor.authorHeeringa P.en
dc.contributor.authorPeleg A.Y.en
dc.contributor.authorRossjohn J.en
dc.contributor.authorHoldsworth S.R.en
dc.contributor.authorKitching A.R.en
dc.contributor.authorOoi J.D.en
dc.contributor.authorJiang J.-H.en
dc.contributor.authorEggenhuizen P.J.en
dc.contributor.authorChua L.L.en
dc.contributor.authorvan Timmeren M.en
dc.contributor.authorLoh K.L.en
dc.contributor.authorO'Sullivan K.M.en
dc.contributor.authorGan P.Y.en
dc.contributor.authorZhong Y.en
dc.contributor.authorTsyganov K.en
dc.contributor.authorShochet L.R.en
dc.contributor.authorStegeman C.A.en
dc.date.accessioned2021-05-14T12:03:02Zen
dc.date.available2021-05-14T12:03:02Zen
dc.date.copyright2019en
dc.date.created20190807en
dc.date.issued2019-08-07en
dc.identifier.citationNature Communications. 10 (1) (no pagination), 2019. Article Number: 3392. Date of Publication: 01 Dec 2019.en
dc.identifier.issn2041-1723 (electronic)en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/35639en
dc.description.abstractAutoreactivity to myeloperoxidase (MPO) causes anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV), with rapidly progressive glomerulonephritis. Here, we show that a Staphylococcus aureus peptide, homologous to an immunodominant MPO T-cell epitope (MPO409-428), can induce anti-MPO autoimmunity. The peptide (6PGD391-410) is part of a plasmid-encoded 6-phosphogluconate dehydrogenase found in some S. aureus strains. It induces anti-MPO T-cell autoimmunity and MPO-ANCA in mice, whereas related sequences do not. Mice immunized with 6PGD391-410, or with S. aureus containing a plasmid expressing 6PGD391-410, develop glomerulonephritis when MPO is deposited in glomeruli. The peptide induces anti-MPO autoreactivity in the context of three MHC class II allomorphs. Furthermore, we show that 6PGD391-410 is immunogenic in humans, as healthy human and AAV patient sera contain anti-6PGD and anti-6PGD391-410 antibodies. Therefore, our results support the idea that bacterial plasmids might have a function in autoimmune disease.Copyright © 2019, The Author(s).en
dc.languageEnglishen
dc.languageenen
dc.publisherNature Publishing Group (Houndmills, Basingstoke, Hampshire RG21 6XS, United Kingdom)en
dc.relation.ispartofNature Communicationsen
dc.titleA plasmid-encoded peptide from Staphylococcus aureus induces anti-myeloperoxidase nephritogenic autoimmunity.en
dc.typeArticleen
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.1038/s41467-019-11255-0en
dc.publisher.placeUnited Kingdomen
dc.identifier.pubmedid31358739 [http://www.ncbi.nlm.nih.gov/pubmed/?term=31358739]en
dc.identifier.source2002357646en
dc.identifier.institution(Ooi, Eggenhuizen, Chua, O'Sullivan, Gan, Zhong, Shochet, Ryan, Holdsworth, Kitching) Centre for Inflammatory Diseases, Monash University Department of Medicine, Monash Medical Centre, Clayton, VIC 3168, Australia (Jiang, Peleg) Infection and Immunity Program, Monash Biomedicine Discovery Institute and Department of Microbiology, Monash University, Clayton, VIC 3800, Australia (van Timmeren, Heeringa) Department of Pathology and Medical Biology, University of Groningen, University Medical Center Groningen, Groningen 9700 RB, Netherlands (Loh, Reid, Rossjohn) Infection and Immunity Program and Department of Biochemistry and Molecular Biology, Biomedicine Discovery Institute, Monash University, Clayton, VIC 3800, Australia (Tsyganov) Monash Bioinformatics Platform, Monash University, Clayton, VIC 3800, Australia (Shochet, Ryan, Holdsworth, Kitching) Department of Nephrology, Monash Health, Clayton, VIC 3168, Australia (Stegeman) Department of Internal Medicine, Division of Nephrology, University of Groningen, University Medical Center Groningen, Groningen 9700 RB, Netherlands (Fugger) Oxford Centre for Neuroinflammation, Nuffield Department of Clinical Neurosciences, and MRC Human Immunology Unit, Weatherall Institute of Molecular Medicine, John Radcliffe Hospital, University of Oxford, Oxford OX3 9DS, United Kingdom (Reid, Rossjohn) Australian Research Council Centre of Excellence in Advanced Molecular Imaging, Monash University, Clayton, VIC 3800, Australia (Rossjohn) Institute of Infection and Immunity, School of Medicine, Cardiff University, Cardiff CF14-4XN, United Kingdom (Peleg) Department of Infectious Diseases, Alfred Hospital and Central Clinical School, Monash University, Melbourne, VIC 3004, Australia (Kitching) NHMRC Centre for Personalised Immunology, Monash University, Clayton, VIC 3168, Australia (Kitching) Department of Pediatric Nephrology, Monash Health, Clayton, VIC 3168, Australia (Chua) Department of Paediatrics, Faculty of Medicine, University of Malaya, Kuala Lumpur 50603, Malaysiaen
dc.description.addressA.R. Kitching, Centre for Inflammatory Diseases, Monash University Department of Medicine, Monash Medical Centre, Clayton, VIC 3168, Australia. E-mail: richard.kitching@monash.eduen
dc.description.publicationstatusEmbaseen
dc.rights.statementCopyright 2019 Elsevier B.V., All rights reserved.en
dc.identifier.authoremailKitching A.R.; richard.kitching@monash.eduen
dc.description.grantNo: 1008849 Organization: (NHMRC) *National Health and Medical Research Council* Organization No: 501100000925 Country: Australia No: 1079648 Organization: (NHMRC) *National Health and Medical Research Council* Organization No: 501100000925 Country: Australia No: 1115805 Organization: (NHMRC) *National Health and Medical Research Council* Organization No: 501100000925 Country: Australiaen
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
crisitem.author.deptNephrology-
crisitem.author.deptImmunology and Allergy-
crisitem.author.deptNephrology-
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