Inoue T, Okumura Y, Shirama M, Ishibashi H, Kashiwagi S, Okubo H
J Clin Immunol. 1986 Mar;6(2):130-5. doi: 10.1007/BF00918745.
Seven patients with selective IgM deficiency (SIgMD) were studied for cell surface immunoglobulin (SmIg), T-cell subpopulations, and immunoglobulin (Ig) synthesis in vitro by peripheral blood lymphocytes (PBL). Serum IgM levels were less than 25 mg/dl, while IgA, IgG, and IgD were within normal levels. The patients had respiratory or urinary tract infections and two were diagnosed as having systemic lupus erythematosus (SLE). T/B-cell ratios in PBL were within normal ranges. Percentage ratios of B cells bearing SmIg were normal in five patients and decreased in two; however, normal values were seen after 7 days of culture in the presence of PWM. OKT4/OKT8 ratios decreased in five of seven patients, in whom two were due to a decrease in OKT4 and two to an increase in OKT8 cells. One showed a decrease in OKT4 and an increase in OKT8. Analysis of lymphocyte function for Ig synthesis in vitro, using a coculture of counterpart T and B cells from healthy individuals and patients with SIgMD, revealed that the increased function of IgM isospecific suppressor T cells (Ts) was responsible for the IgM deficiency in all seven patients.
对7例选择性IgM缺乏症(SIgMD)患者的外周血淋巴细胞(PBL)进行了细胞表面免疫球蛋白(SmIg)、T细胞亚群及体外免疫球蛋白(Ig)合成的研究。血清IgM水平低于25mg/dl,而IgA、IgG和IgD水平正常。患者有呼吸道或泌尿系统感染,2例被诊断为系统性红斑狼疮(SLE)。PBL中T/B细胞比值在正常范围内。5例患者带有SmIg的B细胞百分比正常,2例降低;然而,在有PWM存在的情况下培养7天后可见正常数值。7例患者中有5例OKT4/OKT8比值降低,其中2例是由于OKT4减少,2例是由于OKT8细胞增加。1例表现为OKT4减少和OKT8增加。采用健康个体和SIgMD患者的对应T和B细胞共培养法对体外Ig合成的淋巴细胞功能进行分析,结果显示,所有7例患者的IgM同种特异性抑制性T细胞(Ts)功能增强是导致IgM缺乏的原因。