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dc.contributor.authorLossius, Peter Andreas Volden_US
dc.contributor.authorTomescu-Baciu, Alinaen_US
dc.contributor.authorHolmøy, Trygveen_US
dc.contributor.authorVedeler, Christian A.en_US
dc.contributor.authorRøsjø, Egil Rørviken_US
dc.contributor.authorLorentzen, Åslaug Rudjorden_US
dc.contributor.authorCasetta, Ilariaen_US
dc.contributor.authorVartdal, Frodeen_US
dc.date.accessioned2018-03-27T11:58:35Z
dc.date.available2018-03-27T11:58:35Z
dc.date.issued2017-10
dc.PublishedLossius PAV, Tomescu-Baciu A, Holmøy T, Vedeler CA, Røsjø E, Lorentzen ÅR, Casetta I, Vartdal F. Selective intrathecal enrichment of G1m1-positive B cells in multiple sclerosis. Annals of clinical and translational neurology. 2017;4(10):756-761eng
dc.identifier.issn2328-9503
dc.identifier.urihttps://hdl.handle.net/1956/17567
dc.description.abstractImmunoglobulin gamma (IgG) heavy chain genes are associated with susceptibility to multiple sclerosis (MS) and IgG levels in the cerebrospinal fluid (CSF). However, how these variants are implicated in disease mechanisms remains unknown. Here, we show that proliferating plasmablasts expressing the G1m1 allotype of IgG1 are selectively enriched in CSF of G1m1/G1m3 heterozygous MS patients, whereas plasmablasts expressing either G1m1 or G1m3 are evenly distributed in blood. Moreover, there was a preferential intrathecal synthesis of oligoclonal IgG1 of the G1m1 allotype in heterozygous patients, whereas controls with Lyme neuroborreliosis displayed oligoclonal IgG1 of both allotypes. This points to a disease‐specific mechanism involved in B‐cell establishment within the central nervous system in MS.en_US
dc.language.isoengeng
dc.publisherWileyeng
dc.rightsAttribution CC BY-NC-NDeng
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/eng
dc.titleSelective intrathecal enrichment of G1m1-positive B cells in multiple sclerosisen_US
dc.typePeer reviewed
dc.typeJournal article
dc.date.updated2018-01-11T12:41:08Z
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2017 The Author(s)
dc.identifier.doihttps://doi.org/10.1002/acn3.451
dc.identifier.cristin1508458
dc.source.journalAnnals of clinical and translational neurology


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