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间接血小板放射性抗球蛋白试验联合抗IgG和抗C3在免疫性和非免疫性血小板减少症中的应用

Use of the indirect platelet radioactive antiglobulin test with anti-IgG and anti-C3 in immune and nonimmune thrombocytopenias.

作者信息

Freedman J, Cheong T, Garvey M B

出版信息

Am J Hematol. 1985 Mar;18(3):297-305. doi: 10.1002/ajh.2830180312.

Abstract

Indirect platelet radioactive antiglobulin tests using anti-IgG and anti-C3 were performed in 483 individuals. The subjects' diagnoses and clinical states were correlated with sensitizing protein (IgG and/or C3). Sensitivity of the technique was increased by increasing the serum to cell ratio and there was good correlation between direct and indirect antiglobulin tests in 56 patients. Seven percent of normal healthy non-thrombocytopenic untransfused males and 88% of patients in whom autoimmune thrombocytopenia was clinically suspected showed a positive test result. In the indirect antiglobulin test, mean +/- SD fg anti-C3d/platelet was 1.75 +/- 0.28 (N = 58) with serum from normal subjects, 3.91 +/- 1.86 (N = 123) with serum from patients with idiopathic thrombocytopenic purpura and systemic lupus erythematosus, and 2.78 +/- 0.91 (N = 52) with serum from patients with lymphoproliferative disease. The differences were significant with P less than 0.001. Levels of bound anti-IgG were in general accord with those of other reports; there was no significant relationship with serum immunoglobulin levels. When the indirect antiglobulin tests were positive for both IgG and C3, there was a significant correlation between IgG and C3 bound to normal platelets (r = 0.671; P less than 0.01). Although sera from 39% of patients whose thrombocytopenia was not initially suspected to be on an autoimmune basis gave a positive test result, indirect platelet radioactive antiglobulin tests using anti-IgG and anti-C3 may be convenient tools in the evaluation and follow-up of immune thrombocytopenias.

摘要

对483名个体进行了使用抗IgG和抗C3的间接血小板放射性抗球蛋白试验。将受试者的诊断和临床状态与致敏蛋白(IgG和/或C3)进行关联。通过提高血清与细胞的比例提高了该技术的敏感性,并且在56例患者中直接和间接抗球蛋白试验之间存在良好的相关性。7%的正常健康未输血非血小板减少男性和88%临床怀疑患有自身免疫性血小板减少症的患者检测结果呈阳性。在间接抗球蛋白试验中,正常受试者血清的平均±标准差fg抗C3d/血小板为1.75±0.28(N = 58),特发性血小板减少性紫癜和系统性红斑狼疮患者血清为3.91±1.86(N = 123),淋巴增殖性疾病患者血清为2.78±0.91(N = 52)。差异具有统计学意义,P小于0.001。结合抗IgG的水平总体上与其他报告一致;与血清免疫球蛋白水平无显著关系。当间接抗球蛋白试验IgG和C3均为阳性时,结合到正常血小板上的IgG和C3之间存在显著相关性(r = 0.671;P小于0.01)。尽管最初未怀疑血小板减少是自身免疫性基础的患者中有39%的血清检测结果呈阳性,但使用抗IgG和抗C3的间接血小板放射性抗球蛋白试验可能是评估和随访免疫性血小板减少症的便捷工具。

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