Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/28892
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dc.contributor.authorShochet L.en
dc.contributor.authorKitching A.R.en
dc.contributor.authorHoldsworth S.en
dc.date.accessioned2021-05-14T09:44:19Zen
dc.date.available2021-05-14T09:44:19Zen
dc.date.copyright2020en
dc.date.created20200506en
dc.date.issued2020-05-06en
dc.identifier.citationFrontiers in Immunology. 11 (no pagination), 2020. Article Number: 525. Date of Publication: 09 Apr 2020.en
dc.identifier.issn1664-3224 (electronic)en
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/28892en
dc.description.abstractAnti-neutrophil cytoplasmic antibody (ANCA) associated vasculitis (AAV) is a rare and severe autoimmune multisystemic disease. Its pathogenesis involves multiple arms of the immune system, as well as complex interactions between immune cells and target organs. Experimental animal models of disease can provide the crucial link from human disease to translational research into new therapies. This is particularly true in AAV, due to low disease incidence and substantial disease heterogeneity. Animal models allow for controlled environments in which disease mechanisms can be defined, without the clinical confounders of environmental and lifestyle factors. To date, multiple animal models have been developed, each of which shed light on different disease pathways. Results from animal studies of AAV have played a crucial role in enhancing our understanding of disease mechanisms, and have provided direction toward newer targeted therapies. This review will summarize our understanding of AAV pathogenesis as has been gleaned from currently available animal models, as well as address their strengths and limitations. We will also discuss the potential for current and new animal models to further our understanding of this important condition.© Copyright © 2020 Shochet, Holdsworth and Kitching.en
dc.languageEnglishen
dc.languageenen
dc.publisherFrontiers Media S.A. (E-mail: info@frontiersin.org)en
dc.relation.ispartofFrontiers in Immunologyen
dc.subject.meshpathogenicity-
dc.subject.meshprotein expression-
dc.subject.meshpulmonary vasculitis-
dc.subject.meshregulatory T lymphocyte-
dc.subject.meshspleen cell-
dc.subject.meshTh17 cell-
dc.subject.meshCD18 antigen-
dc.subject.meshcolony stimulating factor-
dc.subject.meshcomplement component C5a receptor-
dc.subject.meshCXCL1 chemokine-
dc.subject.meshCXCL2 chemokine-
dc.subject.meshendothelial leukocyte adhesion molecule 1-
dc.subject.meshimmunoglobulin G-
dc.subject.meshinterleukin 17-
dc.subject.meshinterleukin 8-
dc.subject.meshlipopolysaccharide-
dc.subject.meshlymphocyte function associated antigen 1-
dc.subject.meshlysosome associated membrane protein 2-
dc.subject.meshmannan binding lectin associated serine proteinase-
dc.subject.meshneutrophil cytoplasmic antibody-
dc.subject.meshphosphatidylinositol 3 kinase gamma-
dc.subject.meshtoll like receptor 4-
dc.subject.meshtumor necrosis factor-
dc.subject.meshMBL associated serine protease 2-
dc.subject.meshT lymphocyte-
dc.subject.meshANCA associated vasculitis-
dc.subject.meshantigen antibody complex-
dc.subject.meshautoimmunity-
dc.subject.meshbone marrow cell-
dc.subject.meshCD4+ T lymphocyte-
dc.subject.meshCD8+ T lymphocyte-
dc.subject.meshendothelium injury-
dc.subject.meshextracellular trap-
dc.subject.meshglomerulonephritis-
dc.subject.meshimmune response-
dc.subject.meshleukocyte activation-
dc.titleAnimal Models of ANCA Associated Vasculitis.en
dc.typeReviewen
dc.identifier.affiliationPaediatric - Nephrology-
dc.identifier.affiliationNephrology-
dc.identifier.affiliationImmunology and Allergy-
dc.type.studyortrialReview article (e.g. literature review, narrative review)-
dc.identifier.doihttp://monash.idm.oclc.org/login?url=http://dx.doi.org/10.3389/fimmu.2020.00525-
dc.publisher.placeSwitzerlanden
dc.identifier.pubmedid32373109 [http://www.ncbi.nlm.nih.gov/pubmed/?term=32373109]en
dc.identifier.source631566706en
dc.identifier.institution(Shochet, Holdsworth, Kitching) Centre for Inflammatory Diseases, Monash University, Department of Medicine, Monash Medical Centre, Clayton, VIC, Australia (Shochet, Holdsworth, Kitching) Department of Nephrology, Monash Health, Clayton, VIC, Australia (Holdsworth) Department of Immunology, Monash Health, Clayton, VIC, Australia (Kitching) Department of Pediatric Nephrology, Monash Health, Clayton, VIC, Australiaen
dc.description.addressA.R. Kitching, Centre for Inflammatory Diseases, Monash University, Department of Medicine, Monash Medical Centre, Clayton, VIC, Australia. E-mail: richard.kitching@monash.eduen
dc.description.publicationstatusEmbaseen
dc.rights.statementCopyright 2020 Elsevier B.V., All rights reserved.en
dc.subect.keywordsanimal models antineutrophil cytoplasmic autoantibodies autoimmunity glomerulonephritis myeloperoxidase proteinase 3 translational medical researchen
dc.identifier.authoremailKitching A.R.; richard.kitching@monash.eduen
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.openairetypeReview-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.grantfulltextnone-
crisitem.author.deptNephrology-
crisitem.author.deptImmunology and Allergy-
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