دورية أكاديمية

AB0125 EXPRESSION OF INTERFERON TYPE I- AND TYPE II-INDUCED GENES IN PATIENTS WITH SJÖGREN’S SYNDROME WITH AND WITHOUT EXTRAGLANDULAR INVOLVEMENT

التفاصيل البيبلوغرافية
العنوان: AB0125 EXPRESSION OF INTERFERON TYPE I- AND TYPE II-INDUCED GENES IN PATIENTS WITH SJÖGREN’S SYNDROME WITH AND WITHOUT EXTRAGLANDULAR INVOLVEMENT
المؤلفون: Del Papa, N., Vitali, C., Lorini, M., Carbonelli, V., Maglione, W., Pignataro, F., Minniti, A., Montano, N., Caporali, R.
المصدر: Annals of the Rheumatic Diseases ; volume 79, issue Suppl 1, page 1362.1-1363 ; ISSN 0003-4967 1468-2060
بيانات النشر: BMJ
سنة النشر: 2020
الوصف: Background: It is well known that Sjögren’s syndrome (SjS) is characterized by an upregulation of interferon (IFN)-induced genes. Namely, IFN type I signature has been reported in peripheral blood mononuclear cells (PBMCs) and in salivary glands of patients with this disease. However, few data are available on possible variability of IFN-induced gene upregulation in different clinical phenotypes of SjS. Objectives: To verify whether upregulation of IFN-induced genes is comparable in patients with SjS characterized by different clinical phenotypes, i.e., patients with systemic extraglandular manifestations (EGMs) versus patients with a disease limited to glandular features (GFs) and with widespread pain (WP). Methods: The study population was composed by 11 patients with SjS and EGMs (1 male, age range 18-78 years), and 10 patients with only GFs and WP (all females, age range 46-81 years), all classified according to ACR-EULAR criteria. The prevalence of anti-SSA(Ro) antibodies was 11/11 and 8/10, respectively. Lip biopsy was positive in all cases. Six healthy normal subjects were also included in the study as control population. Four IFN type I- and 5 IFN type II-induced genes were chosen for the study on the basis of previous literature data. Total RNA from each patient and control was isolated from purified PBMCs, followed by cDNA preparation and real time quantitative-PCR (RQ-PCR) analysis, using specific primer/probe sets. For calculation of relative expression, all samples were normalised against expression of a household gene (beta actin). A further normalization was performed against the mean value of relative expression obtained in the normal controls. Final fold change values were determined from the double-normalised values using the 2−ΔΔCT method (Applied Biosystems). Results: Fold change values of gene expression of both IFN type I- and type II-induced genes in PBMCs were different in the two clinical phenotypes of SjS. Fold change values of IFN type I-induced genes appeared strongly higher in ...
نوع الوثيقة: article in journal/newspaper
اللغة: English
DOI: 10.1136/annrheumdis-2020-eular.2845
الإتاحة: https://doi.org/10.1136/annrheumdis-2020-eular.2845Test
رقم الانضمام: edsbas.9F513CE4
قاعدة البيانات: BASE
الوصف
DOI:10.1136/annrheumdis-2020-eular.2845