Marti G E, Ryan E T, Papadopoulos N M, Filling-Katz M, Barton N, Fleischer T A, Rick M, Gralnick H R
Hematology Service, NINCDS, Bethesda, MD 20892.
Am J Hematol. 1988 Dec;29(4):189-94. doi: 10.1002/ajh.2830290403.
Sera from 23 individuals with Gaucher disease (GD) were analyzed for hypergammaglobulinemia and oligoclonal and monoclonal gammopathies. Serum IgG level was elevated in 15/23 (65%) patients, and a diffuse hypergammaglobulinemia was present in 10/23 (43%) patients. An oligoclonal gammopathy was noted in six patients, and a monoclonal gammopathy in two. Lymphocyte subset analysis was also carried out in eight individuals with GD. Four of five individuals showed increased surface Ig-positive lymphocytes, while 7/7 were positive for either increased CD19- and/or CD20-positive lymphocytes. An eighth patient was found to have a B-cell leukemia. Statistical analysis of kappa and lambda histograms were suggestive of a monoclonal excess. However, restriction enzyme analysis of four individuals with GD and increased B cells failed to show any evidence of Ig gene rearrangements. Serum Ig abnormalities and perhaps B-cell lymphocytosis appear to be common in the GD patient population and are not associated with circulating monoclonal lymphocytes.
对23例戈谢病(GD)患者的血清进行了高丙种球蛋白血症、寡克隆和单克隆丙种球蛋白病分析。15/23(65%)的患者血清IgG水平升高,10/23(43%)的患者存在弥漫性高丙种球蛋白血症。6例患者出现寡克隆丙种球蛋白病,2例出现单克隆丙种球蛋白病。还对8例GD患者进行了淋巴细胞亚群分析。5例患者中有4例显示表面Ig阳性淋巴细胞增加,而7/7的患者CD19和/或CD20阳性淋巴细胞增加。第8例患者被发现患有B细胞白血病。kappa和lambda直方图的统计分析提示单克隆过量。然而,对4例GD且B细胞增加的患者进行限制性内切酶分析,未发现Ig基因重排的任何证据。血清Ig异常以及可能的B细胞淋巴细胞增多在GD患者群体中似乎很常见,且与循环单克隆淋巴细胞无关。