Utilize este identificador para referenciar este registo: https://hdl.handle.net/10316/102616
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dc.contributor.authorIvanova, Vilena V-
dc.contributor.authorKhaiboullina, Svetlana F-
dc.contributor.authorCherenkova, Ekaterina E-
dc.contributor.authorMartynova, Ekaterina V-
dc.contributor.authorNevzorova, Tatiana A-
dc.contributor.authorKunst, Michail A-
dc.contributor.authorSibgatullin, Timur B-
dc.contributor.authorMaksudova, Adelia N-
dc.contributor.authorOliveira, Paulo J.-
dc.contributor.authorLombardi, Vincent C-
dc.contributor.authorPalotas, Andras-
dc.contributor.authorRizvanov, Albert A-
dc.date.accessioned2022-10-04T10:01:46Z-
dc.date.available2022-10-04T10:01:46Z-
dc.date.issued2014-
dc.identifier.issn1421-9778pt
dc.identifier.issn1015-8987pt
dc.identifier.urihttps://hdl.handle.net/10316/102616-
dc.description.abstractCirculating auto-reactive antibodies are hallmark features of auto-immune diseases, however little is known with respect to the specificity of such bio-markers. In the present study, we investigated the specificity of anti-nucleic acid antibodies in the blood of subjects with systemic lupus erythematosus (SLE) and healthy controls. Methods: Sera from 12 SLE cases and 8 controls were evaluated for immuno-reactivity to purified RNA, DNA and mitochondrial DNA (mtDNA) by enzyme-linked immuno-sorbent assay (ELISA). Results: As expected, immuno-reactivity to total nucleic acids was significantly higher in subjects with SLE when compared to healthy controls, however a clear distinction was observed among the various nucleic acid sub-types, with sera from SLE subjects displaying the greatest immunoreactivity to RNA followed by mtDNA and then total DNA. Conclusion: The identification of auto-reactive antibodies can serve as highly sensitive biomarkers, although their specificity may not always allow diagnostic certainty. The knowledge that auto-antibodies in subjects with SLE display differential immuno-reactivity may help to improve existing diagnostics and may lead to a better understanding of the pathogenesis of auto-immune disorders.pt
dc.language.isoengpt
dc.relationRussian Government Program of Competitive Growth of Kazan Federal University and funded by the subsidy allocated to Kazan Federal University for the state assignment in the sphere of scientific activities.pt
dc.rightsopenAccesspt
dc.rights.urihttp://creativecommons.org/licenses/by-nc/4.0/pt
dc.subjectAuto-antibodypt
dc.subjectAuto-antigenspt
dc.subjectAuto-immune diseasept
dc.subjectBiomarkerpt
dc.subjectMitochondript
dc.subjectNucleic acidpt
dc.subjectSystemic lupus erythematosus (SLE)pt
dc.subject.meshAdolescentpt
dc.subject.meshAdultpt
dc.subject.meshDNApt
dc.subject.meshDNA, Mitochondrialpt
dc.subject.meshEnzyme-Linked Immunosorbent Assaypt
dc.subject.meshFemalept
dc.subject.meshGenome, Humanpt
dc.subject.meshHEK293 Cellspt
dc.subject.meshHumanspt
dc.subject.meshLupus Erythematosus, Systemicpt
dc.subject.meshMalept
dc.subject.meshMitochondriapt
dc.subject.meshRNApt
dc.titleDifferential immuno-reactivity to genomic DNA, RNA and mitochondrial DNA is associated with auto-immunitypt
dc.typearticle-
degois.publication.firstPage2200pt
degois.publication.lastPage2208pt
degois.publication.issue6pt
degois.publication.titleCellular Physiology and Biochemistrypt
dc.peerreviewedyespt
dc.identifier.doi10.1159/000369663pt
degois.publication.volume34pt
dc.date.embargo2014-01-01*
uc.date.periodoEmbargo0pt
item.fulltextCom Texto completo-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypearticle-
item.grantfulltextopen-
item.cerifentitytypePublications-
crisitem.author.researchunitCNC - Center for Neuroscience and Cell Biology-
crisitem.author.orcid0000-0002-5201-9948-
Aparece nas coleções:I&D CNC - Artigos em Revistas Internacionais
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