Publication:
Is IgG galactosylation the relevant factor for pregnancy-induced remission of rheumatoid arthritis?

cris.virtualsource.author-orcid5f4011fa-bad0-450f-a7ff-8b5307b9929a
cris.virtualsource.author-orcid63f2ef2b-f3c1-408d-90cd-664a146e9c8c
datacite.rightsopen.access
dc.contributor.authorFörger, Frauke
dc.contributor.authorOestensen, Monika Elisabeth
dc.date.accessioned2024-10-10T20:45:45Z
dc.date.available2024-10-10T20:45:45Z
dc.date.issued2010
dc.description.abstractDuring pregnancy, most patients with rheumatoid arthritis (RA) experience spontaneous improvement of their disease activity. Among the soluble candidates that have been investigated in search for the most relevant disease-remitting factor are the galactosylation levels of immunoglobulin G (IgG). In RA, a higher percentage of IgG lacking the terminal galactose residues, thought to play a pro-inflammatory role, is found. During pregnancy, however, IgG galactosylation levels increase and correlate with improved disease activity. The question remains whether the increase in IgG galactosylation during pregnancy is a mere epiphenomenon or a true remission-inducing factor.
dc.description.numberOfPages2
dc.description.sponsorshipUniversitätsklinik für Rheumatologie, klinische Immunologie und Allergologie
dc.identifier.doi10.7892/boris.1654
dc.identifier.isi000278012700008
dc.identifier.pmid20236448
dc.identifier.publisherDOI10.1186/ar2919
dc.identifier.urihttps://boris-portal.unibe.ch/handle/20.500.12422/72370
dc.language.isoen
dc.publisherBioMed Central
dc.publisher.placeLondon
dc.relation.ispartofArthritis research & therapy
dc.relation.issn1478-6354
dc.relation.organizationDCD5A442BAD8E17DE0405C82790C4DE2
dc.titleIs IgG galactosylation the relevant factor for pregnancy-induced remission of rheumatoid arthritis?
dc.typearticle
dspace.entity.typePublication
dspace.file.typetext
oaire.citation.issue1
oaire.citation.startPage108
oaire.citation.volume12
oairecerif.author.affiliationUniversitätsklinik für Rheumatologie, klinische Immunologie und Allergologie
oairecerif.author.affiliationUniversitätsklinik für Rheumatologie, klinische Immunologie und Allergologie
unibe.contributor.rolecreator
unibe.contributor.rolecreator
unibe.description.ispublishedpub
unibe.eprints.legacyId1654
unibe.journal.abbrevTitleARTHRITIS RES THER
unibe.refereedtrue
unibe.subtype.articlecontribution

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