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马其顿人群中人类血小板抗原多态性与特发性血小板减少性紫癜的关联。

Association of polymorphisms in human platelet antigens with idiopathic thrombocytopenic purpura in Macedonians.

作者信息

Pavkovic M, Stojanovic A, Karanfilski O, Cevreska L, Spiroski M

机构信息

University Clinic for Haematology, Medical Faculty, Skopje, R. Macedonia.

出版信息

Prilozi. 2012;33(1):135-46.

Abstract

Idiopathic thrombocytopenic purpura (ITP) is an autoimmune disease characterized by thrombocytopenia due to the presence of platelet autoantibodies specific for platelet membrane glycoproteins, such as GPIIb/IIIa, GPIb/IX and GPIa/IIa. These autoantibodies cause an accelerated clearance of opsonized platelets by phagocytes and inhibition of platelet production. Human platelet antigen (HPA) systems HPA-1, HPA-2, HPA-3 and HPA-5 are components of platelet GP complexes GPIIb/IIIa, GPIb/IX and GPIa/IIa. The HPA system consists of more than 12 bi-allelic antigen polymorphisms in which a base-pair substitution leads to change in an amino acid sequence of a membrane glycoprotein expressed on the platelet surface. The aim of this study was to examine the association of HPA-1, HPA-2, HPA-3 and HPA-5 polymorphisms with idiopathic thrombocytopenic purpura. We performed genotyping of HPA-1, HPA-2, HPA-3, and HPA-5 systems in 60 patients with ITP and 120 healthy participants. Genotyping of HPA-1, -2, -3, and -5 alleles were performed by PCR and RFLP methods by using specific primers and restriction enzymes. Allele and genotype frequencies of HPA-1, HPA-3, and HPA-5 were not significantly different between patients and healthy participants. After Bonferroni adjustment a significant association in ITP patients with HPA-2 alleles (P=0.015, OR=1.923, CI=1.126-3.284) was found. Allele frequencies for HPA-2a were 0.852 in healthy participants and 0.750 in patients, and for HPA-2b 0.148 and 0.250 respectively. These results suggests that HPA-2b allele was more frequent in patients with ITP and may be involved in the formation of a specific autoepitope.

摘要

特发性血小板减少性紫癜(ITP)是一种自身免疫性疾病,其特征为血小板减少,原因是存在针对血小板膜糖蛋白(如糖蛋白IIb/IIIa、糖蛋白Ib/IX和糖蛋白Ia/IIa)的血小板自身抗体。这些自身抗体导致被调理素化的血小板被吞噬细胞加速清除,并抑制血小板生成。人类血小板抗原(HPA)系统HPA-1、HPA-2、HPA-3和HPA-5是血小板糖蛋白复合物糖蛋白IIb/IIIa、糖蛋白Ib/IX和糖蛋白Ia/IIa的组成部分。HPA系统由12种以上的双等位基因抗原多态性组成,其中一个碱基对的替换会导致血小板表面表达的膜糖蛋白氨基酸序列发生变化。本研究的目的是检测HPA-1、HPA-2、HPA-3和HPA-5多态性与特发性血小板减少性紫癜的相关性。我们对60例ITP患者和120名健康参与者进行了HPA-1、HPA-2、HPA-3和HPA-5系统的基因分型。使用特异性引物和限制性内切酶,通过聚合酶链反应(PCR)和限制性片段长度多态性(RFLP)方法对HPA-1、-2、-3和-5等位基因进行基因分型。患者与健康参与者之间HPA-1、HPA-3和HPA-5的等位基因和基因型频率无显著差异。经Bonferroni校正后,发现ITP患者中HPA-2等位基因存在显著相关性(P=0.015,OR=1.923;CI=1.126-3.284)。健康参与者中HPA-2a的等位基因频率为0.852;患者中为0.750,HPA-2b的等位基因频率分别为0.148和0.250。这些结果表明,HPA-2b等位基因在ITP患者中更为常见,可能参与了特定自身表位的形成。

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