Umehara Hisanori, Sawaki Toshioki, Kawanami Takafumi, Masaki Yasufumi, Fukushima Tosihiro
Division of Hematology and Immunology, Kanazawa Medical University.
Nihon Rinsho. 2009 Mar;67(3):511-6.
Sjögren's syndrome (SS) is chronic autoimmune disease characterized by destructive lymphocyte infiltration of salivary and lacrimal glands, which results in dry eyes and dry mouth. Despite extensive study of the underlying cause of SS, the pathogenesis remains obscure. The Sjögren's International Collaborative Clinical Alliance (SICCA) by five Research Groups located in Argentina, China, Denmark, the United States and Japan, is the first registry and clinical data-specimen repository to establish the International Standard Criteria for diagnosing SS. Patients with SS have a relative increased risk for development of B cell lymphoma compared with other autoimmune rheumatic diseases. We discuss the possible mechanisms for lymphoma development. The topics concerning SS is IgG4-related lymphoproliferative diseases, such as Mikulicz's disease and autoimmune pancreatitis. Based on the analysis of patients registered from all over Japan, we propose a new clinical entity IgG4-positive multi-organ lymphoproliferative syndrome (IgG4+ MOLPS).
干燥综合征(SS)是一种慢性自身免疫性疾病,其特征是唾液腺和泪腺出现破坏性淋巴细胞浸润,导致眼睛干涩和口干。尽管对SS的潜在病因进行了广泛研究,但其发病机制仍不清楚。由位于阿根廷、中国、丹麦、美国和日本的五个研究小组组成的干燥综合征国际协作临床联盟(SICCA),是首个建立诊断SS国际标准的登记处和临床数据样本库。与其他自身免疫性风湿性疾病相比,SS患者发生B细胞淋巴瘤的风险相对增加。我们讨论了淋巴瘤发生的可能机制。与SS相关的主题是IgG4相关的淋巴增殖性疾病,如米库利奇病和自身免疫性胰腺炎。基于对来自日本各地登记患者的分析,我们提出了一种新的临床实体IgG4阳性多器官淋巴增殖综合征(IgG4+ MOLPS)。