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对奎宁和奎尼丁诱导的免疫性血小板减少症患者淋巴细胞培养中引起特异性转化的因素的研究。

Study of the factors that cause specific transformation in cultures of lymphocytes from patients with quinine- and quinidine-induced immune thrombocytopenia.

作者信息

Hosseinzadeh P K, Firkin B G, Pfueller S L

出版信息

J Clin Invest. 1980 Oct;66(4):638-45. doi: 10.1172/JCI109899.

Abstract

Quinine- or quinidine-induced thrombocytopenic purpura is caused by synthesis of an immunoglobulin (Ig)G antibody, which caused platelet damage in the presence of the offending drug. The nature of the antigenic stimulus has been examined by measuring incorporation of [3H]thymidine into DNA during lymphocyte transformation to blast cells in the presence of the drug. Although patients' lymphocytes responded normally to the nonspecific mitogen, phytohemagglutinin P, they did not respond to either drug or platelets alone. However, significant transformation occurred when patients' lymphocytes were cultured for 7 d with homologous or autologous platelets in the presence of therapeutic concentrations of the drugs (0.39-39 microM). Platelet membranes were more active than intact platelets on the basis of protein content, whereas platelets from a patient with Bernard-Soulier syndrome were inactive. Washed platelets pretreated with the drugs were inactive when cultured with lymphocytes in the absence of the drugs, whereas platelets pretreated similarly in plasma caused transformation. Control lymphocytes from 20 normal patients and 6 patients with nondrug-induced thrombocytopenia were not transformed by drugs and platelets in the presence of normal serum or serum containing drug-dependent antibody, showing that the observed response was specific for presensitized lymphocytes. Thus lymphocytes of patients with drug-induced thrombocytopenia are transformed by an antigen that forms after interaction of plasma, specific platelet membrane components and the drug.

摘要

奎宁或奎尼丁诱导的血小板减少性紫癜是由一种免疫球蛋白(Ig)G抗体的合成引起的,该抗体在存在致病药物的情况下导致血小板损伤。通过在药物存在下测量淋巴细胞转化为母细胞过程中[3H]胸腺嘧啶核苷掺入DNA的情况,研究了抗原刺激的性质。尽管患者的淋巴细胞对非特异性有丝分裂原植物血凝素P反应正常,但它们对单独的药物或血小板均无反应。然而,当患者的淋巴细胞在治疗浓度的药物(0.39 - 39 microM)存在下与同源或自体血小板培养7天时,会发生显著的转化。基于蛋白质含量,血小板膜比完整血小板更具活性,而来自伯纳德 - 索利尔综合征患者的血小板则无活性。在无药物的情况下与淋巴细胞培养时,用药物预处理的洗涤血小板无活性,而在血浆中进行类似预处理的血小板则会导致转化。在正常血清或含有药物依赖性抗体的血清存在下,来自20名正常患者和6名非药物诱导的血小板减少症患者的对照淋巴细胞不会被药物和血小板转化,这表明观察到的反应对预先致敏的淋巴细胞具有特异性。因此,药物诱导的血小板减少症患者的淋巴细胞会被一种在血浆、特定血小板膜成分和药物相互作用后形成的抗原所转化。

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