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dc.creatorPapageorgiou A., Mavragani C.P., Nezos A., Zintzaras E., Quartuccio L., De Vita S., Koutsilieris M., Tzioufas A.G., Moutsopoulos H.M., Voulgarelis M.en
dc.date.accessioned2023-01-31T09:42:54Z
dc.date.available2023-01-31T09:42:54Z
dc.date.issued2015
dc.identifier10.1002/ART.39231
dc.identifier.issn23265191
dc.identifier.urihttp://hdl.handle.net/11615/77655
dc.description.abstractObjective. To study the prevalence, clinical associations, and functional implications of the His159Tyr mutation of the BAFF receptor (BAFF-R) in patients with Sjögren’s syndrome (SS). Methods. The BAFF-R His159Tyr mutation was evaluated using polymerase chain reaction (PCR)-based assays in 247 patients with SS (of whom 70 had SS complicated by lymphoma [SS-lymphoma]), 145 with systemic lupus erythematosus (SLE), and 101 with rheumatoid arthritis (RA), as well as 180 healthy controls. Real-time PCR and Western blotting were performed for the quanti fication of both NF-kB1 and NF-kB2 messenger RNA (mRNA) transcript and protein levels in isolated B cells from patients with SS-lymphoma carrying the mutation (SS-lymphoma-BAFF-RHis159Tyr-derived B cells) compared to B cells from patients with SS-lymphoma who were not carriers of the mutation and healthy controls. Results. Both the SS-lymphoma and SS-nonlymphoma patient subgroups exhibited significantly higher frequencies of the His159Tyr BAFF-R mutation compared to healthy controls (8.6% of SS-lymphoma patients and 6.2% of SS-nonlymphoma patients versus 1.7% of healthy controls; P = 0.02 and P = 0.04, respectively). The corresponding frequencies of the His159Tyr BAFF-R mutation in SLE and RA patients were 3.5% and 3%, respectively. Of interest, 71.4% of the SS patients with mucosa-associated lymphoid tissue (MALT) lymphoma who were between the ages of 31 and 40 years at disease onset were mutation carriers. The generalized odds ratio for the development of SS-related MALT lymphoma in the younger age at onset (age <40 years) group in the presence of the BAFF-R mutation was 6.1 (95% confidence interval 2.0-18.7) (P < 0.01). Expression of NF-kB at both the mRNA and protein level was up-regulated in SS-lymphoma-BAFF-RHis159Tyr-derived B cells. Conclusion. This study identifies an increased prevalence of the BAFF-R His159Tyr mutation in patients with SS, particularly in those with SS complicated by MALT lymphoma whose disease onset occurred at a younger age. BAFF-RHis159Tyr-mediated activation of the alternate NF-kB pathway might contribute to the pathogenesis of SS-related lymphoproliferative disease. © 2015, American College of Rheumatology.en
dc.language.isoenen
dc.sourceArthritis and Rheumatologyen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-84988864510&doi=10.1002%2fART.39231&partnerID=40&md5=16df07d98a53659f8f5a6de0a5921ba7
dc.subjectB cell activating factor receptoren
dc.subjectimmunoglobulin enhancer binding proteinen
dc.subjectadulten
dc.subjectageden
dc.subjectArthritis, Rheumatoiden
dc.subjectcase control studyen
dc.subjectcomplicationen
dc.subjectfemaleen
dc.subjectgenetic predispositionen
dc.subjectgeneticsen
dc.subjectheterozygoteen
dc.subjecthumanen
dc.subjectLupus Erythematosus, Systemicen
dc.subjectLymphoproliferative Disordersen
dc.subjectmaleen
dc.subjectmarginal zone lymphomaen
dc.subjectmiddle ageden
dc.subjectmutationen
dc.subjectphysiologyen
dc.subjectprevalenceen
dc.subjectsignal transductionen
dc.subjectSjogren's Syndromeen
dc.subjectAdulten
dc.subjectAgeden
dc.subjectArthritis, Rheumatoiden
dc.subjectB-Cell Activation Factor Receptoren
dc.subjectCase-Control Studiesen
dc.subjectFemaleen
dc.subjectGenetic Predisposition to Diseaseen
dc.subjectHeterozygoteen
dc.subjectHumansen
dc.subjectLupus Erythematosus, Systemicen
dc.subjectLymphoma, B-Cell, Marginal Zoneen
dc.subjectLymphoproliferative Disordersen
dc.subjectMaleen
dc.subjectMiddle Ageden
dc.subjectMutationen
dc.subjectNF-kappa Ben
dc.subjectPrevalenceen
dc.subjectSignal Transductionen
dc.subjectSjogren's Syndromeen
dc.subjectJohn Wiley and Sons Incen
dc.titleA BAFF Receptor His159Tyr Mutation in Sjögren’s Syndrome-Related Lymphoproliferationen
dc.typejournalArticleen


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