Burger T, Balázs L, Schmelczer M, Molnár L, Török L, Fábián G
Second Department of Medicine, University Medical School, Pécs, Hungary.
Acta Med Hung. 1987;44(2-3):243-56.
Data gained from observations of the humoral and cellular immunity of 22 patients with ITP (11 in remission and 11 splenectomised) are presented. The amount of T-lymphocytes according to E-rosetting decreased significantly. In tests performed with monoclonal sera the amount of OKT-4 cells was significantly lower then normal, and the ratio of OKT-4/OKT-8 was also reduced. The C-4 complement fraction showed a significant reduction, and a rise was observed in the three Ig classes. No differences could be found, however, between patients in remission and in relapse, and between the splenectomised cases, those treated with prednisolone, and those who had no such treatment. Apart from the primary role of antiplatelet antibodies that cause thrombopenia, a complex disturbance in immune regulation also occurred in ITP, and this manifested with changes in the T-lymphocyte subpopulations. Its pathological progress still remains to be justified, but the plasma of healthy individuals and gammaglobulin have a favorable effect by blocking their receptors and they result in the cessation of the symptom and thrombocytopenia.
本文呈现了对22例特发性血小板减少性紫癜患者(11例缓解期患者和11例脾切除患者)体液免疫和细胞免疫观察所获得的数据。根据E花环试验,T淋巴细胞数量显著减少。在用单克隆血清进行的检测中,OKT - 4细胞数量显著低于正常水平,且OKT - 4/OKT - 8比值也降低。C - 4补体成分显著减少,三种免疫球蛋白类别均有升高。然而,缓解期患者与复发患者之间,以及脾切除病例、接受泼尼松龙治疗的病例与未接受此类治疗的病例之间未发现差异。除了抗血小板抗体导致血小板减少的主要作用外,特发性血小板减少性紫癜还出现了免疫调节的复杂紊乱,这表现为T淋巴细胞亚群的变化。其病理进展仍有待阐明,但健康个体的血浆和丙种球蛋白通过阻断其受体产生有益作用,从而导致症状和血小板减少症停止。