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Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
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A BAFF Receptor His159Tyr Mutation in Sjögren’s Syndrome-Related Lymphoproliferation

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Συγγραφέας
Papageorgiou A., Mavragani C.P., Nezos A., Zintzaras E., Quartuccio L., De Vita S., Koutsilieris M., Tzioufas A.G., Moutsopoulos H.M., Voulgarelis M.
Ημερομηνία
2015
Γλώσσα
en
DOI
10.1002/ART.39231
Λέξη-κλειδί
B cell activating factor receptor
immunoglobulin enhancer binding protein
adult
aged
Arthritis, Rheumatoid
case control study
complication
female
genetic predisposition
genetics
heterozygote
human
Lupus Erythematosus, Systemic
Lymphoproliferative Disorders
male
marginal zone lymphoma
middle aged
mutation
physiology
prevalence
signal transduction
Sjogren's Syndrome
Adult
Aged
Arthritis, Rheumatoid
B-Cell Activation Factor Receptor
Case-Control Studies
Female
Genetic Predisposition to Disease
Heterozygote
Humans
Lupus Erythematosus, Systemic
Lymphoma, B-Cell, Marginal Zone
Lymphoproliferative Disorders
Male
Middle Aged
Mutation
NF-kappa B
Prevalence
Signal Transduction
Sjogren's Syndrome
John Wiley and Sons Inc
Εμφάνιση Μεταδεδομένων
Επιτομή
Objective. 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.
URI
http://hdl.handle.net/11615/77655
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