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HLA-DPB_1等位基因与特发性血小板减少性紫癜的相关性研究

ASSOCIATON BETWEEN HLA-DPB_1 GENE ANDIDOPATHC THROMBOCYTOPENIC PURPURA
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摘要 采用多聚酶链反应(PCR)结合限制性片段长度多态性(RFLP)技术对53例正常人和55例慢性特发性血小板减少性紫癜(ITP)患者进行HLA-DPB_1等位基因分型。结果显示,对照组无一例有DPB_11301等位基因,ITP组6例存在DPB_11301等位基因(RR=14.02,P<0.05),此外,DPB_10201+0202所对应的DP_(w2)抗原纯合子在ITP组明显多于对照组(RR=3.94,P<0.01),而DP_(w2)杂合子明显少于对照组(P<0.025),提示DPB_11301等位基因及DP_(w2)抗原纯合子可能与ITP的易感性有关,而DP_(w2)抗原杂合子可能具有保护作用。 enomic HLA-DPB_1 typing of 53 unrelated Chi-nese blcod donors and 55 ITP patients was performed byusing polyrnerase chain reaction (PCR) followed by re-striction fragment length polymorphism (RFLP) analy-sis. The primers used in PCR were designed to anneal toflanking region of the second exon of DPB_1 gene . Allelicspecificity was determined by electrophoretic analysis ofthe pattern of restriction fragments which were generat-ed by digestion with several restriction endonucleases.The results showed that the frequencies of DPB_1 0501and DPB_1 0201 + 0202 allelles in Chinese were muchhigher, and the frequencies of DPB_1 and DPB_1 0401+0402 alleles were mere much lower than those in Cau-cacians. An increased frequency of DPB_1 1301 in pa-tients with ITP was revealed as compared with normalcontrols (RR =14. 02 , P<0. 05) . In addition , DPw_2homozygotes in ITP were much more than those in con-trols (P<0. 025). It suggested that DPB_1 1301 alleleand DPw_2 homozygosity may be associated with ITP-susceptibility , and DPw_2 heterozygosity may be protec-tive against the development of ITP.
出处 《中华血液学杂志》 CAS CSCD 北大核心 1995年第3期118-121,共4页 Chinese Journal of Hematology
基金 江苏省科委资助
关键词 紫癜 血小板减少 人白细胞抗原 多聚酶链反应 Idiopathic thrombocytopenic purpuraHLA-DP DNA-typing
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参考文献3

  • 1Gao X,Arthritis Rheum,1991年,34卷,1310页
  • 2张源慧,中华血液学杂志,1991年,12卷,61页
  • 3Lee T D,The HLA System,1990年

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