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Anti-neutrophil cytoplasmic antibody-associated systemic vasculitis: Nature or nurture?

dc.contributor.authorGatenby, Paul
dc.date.accessioned2015-12-07T22:47:56Z
dc.date.issued2011
dc.date.updated2016-02-24T11:32:01Z
dc.description.abstractThis review examines the environmental and genetic contributions to the anti-neutrophil cytoplasmic antibody-associated systemic vasculitides. The dominant environmental risk factors appear to be silica exposure for all three syndromes, and vitamin D deficiency is strongly suggested by the latitude and ultraviolet radiation gradient observed for Wegener's granulomatosis and Churg-Strauss syndrome. Genetic factors are generally not very strong, consistent with the rarity of these conditions in children. However, multiple genetic factors, each with a relatively small effect, may combine to create a state of susceptibility towards autoimmunity. With infection as a triggering agent, it is possible to synthesise a pathogenetic hypothesis that accounts for both environmental and genetic effects in regard to both necrotising vasculitis and granuloma formation.
dc.identifier.issn1444-0903
dc.identifier.urihttp://hdl.handle.net/1885/26270
dc.publisherBlackwell Science Asia
dc.sourceInternal Medicine Journal
dc.subjectKeywords: neutrophil cytoplasmic antibody; age distribution; ecology; environmental factor; ethnic difference; genetics; human; infection; latitude; necrotizing arteritis; priority journal; review; risk assessment; rural area; sex difference; synthesis; systemic va Anti-neutrophil cytoplasmic antibody; Genetics; Silica; Vasculitis; Vitamin D
dc.titleAnti-neutrophil cytoplasmic antibody-associated systemic vasculitis: Nature or nurture?
dc.typeJournal article
local.bibliographicCitation.issue4
local.bibliographicCitation.lastpage359
local.bibliographicCitation.startpage351
local.contributor.affiliationGatenby, Paul, College of Medicine, Biology and Environment, ANU
local.contributor.authoruidGatenby, Paul, u4044018
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.identifier.absfor110701 - Allergy
local.identifier.absfor110300 - CLINICAL SCIENCES
local.identifier.ariespublicationu4971216xPUB43
local.identifier.citationvolume42
local.identifier.doi10.1111/j.1445-5994.2011.02705.x
local.identifier.scopusID2-s2.0-84859828872
local.identifier.thomsonID000302796000008
local.type.statusPublished Version

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