Raziuddin S, Madan A, Danial B H
Department of Immunology, King Saud University, College of Medicine, Abha Saudi Arabia.
Scand J Immunol. 1987 Nov;26(5):487-93. doi: 10.1111/j.1365-3083.1987.tb02282.x.
A patient with chronic lymphocytic leukaemia and elevated serum IgM antibody is described. A multiparameter surface marker analysis of his peripheral blood lymphocytes demonstrated a unique phenotype of OKT3-, OKT11+, E-rosetting+, OKT4-, OKT8+, OKIa1+, OKCLL+, OKDR+, Tac+, characterizing the disease as suppressor (CD8+) T cell chronic lymphocytic leukaemia. Because of the uncommon phenotype and the abnormal serum immunoglobulin pattern, in vitro functional assays were performed that showed decreased mitogenic response to the phytohaemagglutinin, but increased response to concanavalin A. However, these leukaemic T cells demonstrated phytohaemagglutinin-specific suppressor cell activity on normal blood lymphocytes. In vitro functional studies indicated that a defect in the patient's T cells may cause IgM hypergammaglobulinaemia. The regulatory function of the patient's T cells on immunoglobulin synthesis by normal B cells was found to be mediated by a soluble factor secreted from neoplastic T cells.
本文描述了一位患有慢性淋巴细胞白血病且血清IgM抗体升高的患者。对其外周血淋巴细胞进行的多参数表面标志物分析显示出独特的表型:OKT3-、OKT11+、E花环阳性、OKT4-、OKT8+、OKIa1+、OKCLL+、OKDR+、Tac+,将该疾病特征化为抑制性(CD8+)T细胞慢性淋巴细胞白血病。由于这种不常见的表型和异常的血清免疫球蛋白模式,进行了体外功能测定,结果显示对植物血凝素的促有丝分裂反应降低,但对刀豆球蛋白A的反应增强。然而,这些白血病T细胞对正常血液淋巴细胞表现出植物血凝素特异性抑制细胞活性。体外功能研究表明,患者T细胞的缺陷可能导致IgM高丙种球蛋白血症。发现患者T细胞对正常B细胞免疫球蛋白合成的调节功能是由肿瘤性T细胞分泌的一种可溶性因子介导的。