Sugai S, Konda S, Shoraski Y, Murayama T, Nishikawa T
Am J Med. 1980 Jun;68(6):861-6. doi: 10.1016/0002-9343(80)90215-6.
Two Japanese patients with Sjögren's syndrome with non-immunoglobulin M(IgM) class monoclonal gammopathy are described. The monoclonal IgA lambda detected in the serum and saliva was confirmed to possess rheumatoid factor activity in the first patient with a hypergammaglobulinemic purpura and hyperviscosity syndrome. Idiotype specificity was present on the surface membrane of peripheral blood lymphocytes as well as in the cytoplasm of infiltrating cells in the salivary glands. Common idiotypic specificity was found in four of 60 other patients who had rheumatoid factors. In the serum and saliva of the other patient, a monoclonal immunoglobulin G, kappa type (IgG kappa), was detected. Kappa type IgG was found in most of the infiltrating cells in the salivary glands and also in the saline extract from a resected submandibular gland. Our findings indicate that non-IgM class monoclonal gammopathy is also one of the complications of Sjögren's syndrome.
本文描述了两名患有干燥综合征且伴有非免疫球蛋白M(IgM)类单克隆丙种球蛋白病的日本患者。在首例患有高球蛋白血症性紫癜和高黏滞综合征的患者中,血清和唾液中检测到的单克隆IgAλ被证实具有类风湿因子活性。独特型特异性存在于外周血淋巴细胞的表面膜以及唾液腺浸润细胞的细胞质中。在其他60名患有类风湿因子的患者中,有4名发现了共同独特型特异性。在另一名患者的血清和唾液中,检测到一种单克隆免疫球蛋白G,κ型(IgGκ)。κ型IgG在唾液腺的大多数浸润细胞中以及切除的下颌下腺的盐水提取物中均有发现。我们的研究结果表明,非IgM类单克隆丙种球蛋白病也是干燥综合征的并发症之一。