Schubert J, Uciechowski P, Delany P, Tischler H J, Kolanus W, Schmidt R E
Abt. Immunologie und Transfusionsmedizin, Medizinische Hochschule Hannover, Federal Republic of Germany.
Blood. 1990 Sep 15;76(6):1181-7.
Paroxysmal nocturnal hemoglobinuria (PNH) is clinically characterized by intravascular hemolysis, hemoglobinuria, iron deficiency anemia, and venous thrombosis. Pathophysiologically the disease has now been generally accepted as an acquired defect of phosphatidylinositol glycan (PIG)-anchored molecules on the cell surface of bone marrow-derived cells. This defect is functionally characterized by an abnormal susceptibility to complement-mediated lysis and has been described on erythrocytes, granulocytes, monocytes, and platelets. In contrast, contradictory data exist so far on the involvement of lymphocytes and natural killer (NK) cells. Using monoclonal antibodies (MoAbs) against newly defined PIG-linked surface structures such as CD48, CD55, and CD59, which are homogeneously expressed on lymphocytes of normal donors, we analyzed lymphocytes and their subpopulations in nine PNH patients by two color immunofluorescence. Our results showed that CD3+ T cells as well as CD16+ NK cells are at least partially involved in the deficient PIG-molecule surface expression. To more clearly define the defect in PNH, we generated NK clones from a PNH patient. Phenotypic analysis of these NK clones showed that they either were positive (n = 3) for PIG-linked surface structures such as CD48, CD55, and CD59 (eg, NKP1) or were completely negative (n = 7) for all of them (eg, NKP1). In functional tests the PIG-molecule negative clone NKP2 showed increased susceptibility to human complement compared with the PIG molecule positive clone NKP1. When analyzing the mRNA levels of the PIG-linked molecules CD55 and CD59 there was no difference at all between the two clones. We conclude from our data that NK cells as well as other lymphocyte subpopulations are involved in the PIG-linkage defect of PNH. These NK clones with differential expression of PIG-linked surface structures present for the first time ex vivo mutant cell lymphocyte lines that carry the defect leading to PIG deficiency in PNH.
阵发性睡眠性血红蛋白尿症(PNH)的临床特征为血管内溶血、血红蛋白尿、缺铁性贫血和静脉血栓形成。从病理生理学角度来看,该疾病现已被普遍认为是骨髓来源细胞表面磷脂酰肌醇聚糖(PIG)锚定分子的后天性缺陷。这种缺陷在功能上的特征是对补体介导的溶解异常敏感,并且已在红细胞、粒细胞、单核细胞和血小板中得到描述。相比之下,关于淋巴细胞和自然杀伤(NK)细胞的参与情况,目前存在相互矛盾的数据。我们使用针对新定义的PIG连接表面结构(如CD48、CD55和CD59)的单克隆抗体(MoAb),这些结构在正常供体的淋巴细胞上均匀表达,通过双色免疫荧光分析了9例PNH患者的淋巴细胞及其亚群。我们的结果表明,CD3 + T细胞以及CD16 + NK细胞至少部分参与了PIG分子表面表达缺陷。为了更清楚地界定PNH中的缺陷,我们从一名PNH患者中生成了NK克隆。对这些NK克隆的表型分析表明,它们要么对PIG连接表面结构(如CD48、CD55和CD59)呈阳性(n = 3)(例如NKP1),要么对所有这些结构完全呈阴性(n = 7)(例如NKP2)。在功能测试中,与PIG分子阳性克隆NKP1相比,PIG分子阴性克隆NKP2对人补体的敏感性增加。在分析PIG连接分子CD55和CD59的mRNA水平时,两个克隆之间根本没有差异。我们从数据中得出结论,NK细胞以及其他淋巴细胞亚群参与了PNH的PIG连接缺陷。这些具有PIG连接表面结构差异表达的NK克隆首次在体外呈现出携带导致PNH中PIG缺乏缺陷的突变细胞淋巴细胞系。