Hegde U M, Williams K, Devereux S, Bowes A, Powell D, Fisher D
Clin Lab Haematol. 1983;5(1):9-15. doi: 10.1111/j.1365-2257.1983.tb00491.x.
Thrombocytopenia is frequently encountered in patients with lymphoproliferative disorders (LPD) and systemic erythromatosus (SLE) and to a lesser extent in association with other diseases such as rheumatoid arthritis (RA), pernicious anaemia (PA) and autoimmune haemolytic anaemia (AIHA). This report attempts to document the incidence of thrombocytopenia in these disorders, other than that overtly due to malignant infiltration or marrow suppression by drugs and to demonstrate, that in a significant proportion antibody mediated immune destruction of platelets can be confirmed by positive platelet antibody tests. Platelet associated IgG (PAIgG) was measured in all patients by a quantitative enzyme linked assay. Platelet antibodies were found in 11 of 24 (46%) thrombocytopenic patients with LPD, 10 of 16 (62%) patients with SLE and thrombocytopenia, and in all patients with RA and PA who had low platelet counts at the time of study. In addition, elevated PAIgG levels were found in the following non-thrombocytopenic patients: 9 of 43 (21%) patients with LPD, 2 of 12 (17%) with SLE, 2 of 12 (17%) with AIHA, 2 of 39 (5%) with PA and 5 of 61 (8%) patients with RA. The nature and the role of raised PAIgG levels in diseases other than autoimmune thrombocytopenia is controversial. Our reasons for interpreting these as true platelet autoantibodies in this selected group of disorders and the clinical implications of our results are discussed.
血小板减少症在淋巴增生性疾病(LPD)和系统性红斑狼疮(SLE)患者中经常出现,在类风湿性关节炎(RA)、恶性贫血(PA)和自身免疫性溶血性贫血(AIHA)等其他疾病中出现的程度较轻。本报告试图记录这些疾病中血小板减少症的发生率,而非明显由恶性浸润或药物骨髓抑制导致的血小板减少症发生率,并证明在相当一部分患者中,血小板抗体检测呈阳性可证实血小板的抗体介导免疫破坏。通过定量酶联免疫吸附测定法对所有患者的血小板相关IgG(PAIgG)进行了检测。在24例LPD血小板减少症患者中有11例(46%)、16例SLE合并血小板减少症患者中有10例(62%)以及研究时血小板计数低的所有RA和PA患者中均发现了血小板抗体。此外,在以下非血小板减少症患者中也发现了PAIgG水平升高:43例LPD患者中有9例(21%)、12例SLE患者中有2例(17%)、12例AIHA患者中有2例(17%)、39例PA患者中有2例(5%)以及61例RA患者中有5例(8%)。PAIgG水平升高在自身免疫性血小板减少症以外的疾病中的性质和作用存在争议。本文讨论了将这些PAIgG水平升高解释为所选疾病组中真正血小板自身抗体的原因以及我们研究结果的临床意义。