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儿童特发性血小板减少性紫癜中抗血小板糖蛋白抗原IIb/IIIa自身抗体的特征分析

Characterization of autoantibodies against the platelet glycoprotein antigens IIb/IIIa in childhood idiopathic thrombocytopenia purpura.

作者信息

Taub J W, Warrier I, Holtkamp C, Beardsley D S, Lusher J M

机构信息

Division of Pediatric Hematology/Oncology, Children's Hospital of Michigan.

出版信息

Am J Hematol. 1995 Feb;48(2):104-7. doi: 10.1002/ajh.2830480207.

DOI:10.1002/ajh.2830480207
PMID:7847322
Abstract

The majority of children with idiopathic thrombocytopenia (ITP) have an acute self-limiting course and no diagnostic test has been identified which will predict the course of thrombocytopenia and detect those with the chronic autoimmune form. The detection of autoantibodies directed against the platelet glycoprotein complex IIB/IIIa, may identify patients with chronic ITP. Serum anti-GP IIb/IIIa antibodies were assessed by the indirect MAIPA assay in 54 children with immune thrompocytopenia at initial presentation along with an additional 7 children previously diagnosed with chronic ITP, to determine if there was a difference in antibody positivity between acute and chronic ITP patients, and whether the identification of antibodies could be used as a predictive test at diagnosis. There was no significant difference in the percentage of antibodies detected in children classified with acute ITP (27/40-68%) compared to children with chronic ITP (13/21-62%, P > 0.05). Patients with acute ITP had significantly lower mean platelet counts at diagnosis compared to the chronic ITP group (16,225/mm3 vs 32,250/mm3, P < 0.05), though there was no significant difference in the bleeding manifestations between the acute and chronic ITP groups. Serum anti-GP IIb/IIIa antibodies are detected in a high percentage of children with ITP and autoantibodies appear to be involved in the pathogenesis of both acute and chronic ITP. The detection of anti-GP IIb/IIIa antibodies at diagnosis, however, does not appear to be a useful prognostic test in childhood ITP.

摘要

大多数特发性血小板减少症(ITP)患儿病程呈急性自限性,尚未发现可预测血小板减少病程及检测慢性自身免疫性形式患者的诊断性检查。检测针对血小板糖蛋白复合物IIb/IIIa的自身抗体,可能有助于识别慢性ITP患者。采用间接单克隆抗体固相血小板抗原固定试验(MAIPA)对54例初诊免疫性血小板减少症患儿及另外7例先前诊断为慢性ITP的患儿进行血清抗GP IIb/IIIa抗体评估,以确定急性和慢性ITP患者之间抗体阳性率是否存在差异,以及抗体检测能否作为诊断时的预测性检查。与慢性ITP患儿(13/21 - 62%)相比,急性ITP患儿中检测到抗体的百分比无显著差异(27/40 - 68%,P>0.05)。急性ITP患者诊断时的平均血小板计数显著低于慢性ITP组(16,225/mm³对32,250/mm³,P<0.05),尽管急性和慢性ITP组之间出血表现无显著差异。ITP患儿中高比例检测到血清抗GP IIb/IIIa抗体,自身抗体似乎参与了急性和慢性ITP的发病机制。然而,诊断时检测抗GP IIb/IIIa抗体似乎并非儿童ITP的有用预后检查。

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