Reksten Tove R, Jonsson Malin V
Broegelmann Research Laboratory, Department of Clinical Science, University of Bergen, The Laboratory Building, 5th Floor, Haukeland University Hospital, Bergen N-5021, Norway.
Oral Maxillofac Surg Clin North Am. 2014 Feb;26(1):1-12. doi: 10.1016/j.coms.2013.09.002.
Primary Sjögren's syndrome (pSS) is an autoimmune chronic inflammatory disorder affecting 0.2% to 3.0% of the population, with a 9:1 female to male ratio. Features are oral and ocular dryness, local and systemic autoantibody production, and progressive focal mononuclear cell infiltration in the affected salivary and lacrimal glands. Lymphoma is the most severe complication of pSS, occurring in 4% to 5% of patients. Genetic studies identified an association with HLA and susceptibility genes in cytokine genes and genes involved in B-cell differentiation. Genetic variations may help explain why disease manifestations differ among patients and supports the hypothesis of certain distinct disease phenotypes.
原发性干燥综合征(pSS)是一种自身免疫性慢性炎症性疾病,影响0.2%至3.0%的人群,男女比例为9:1。其特征为口腔和眼部干燥、局部和全身自身抗体产生,以及受累唾液腺和泪腺中进行性局灶性单核细胞浸润。淋巴瘤是pSS最严重的并发症,发生在4%至5%的患者中。基因研究确定了其与HLA以及细胞因子基因和参与B细胞分化的基因中的易感基因有关。基因变异可能有助于解释为什么患者之间的疾病表现不同,并支持某些不同疾病表型的假说。