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HEREDITAS ›› 2007, Vol. 29 ›› Issue (2): 177-177―179.doi: 10.1360/yc-007-0177

• 研究报告 • Previous Articles     Next Articles

Case report of a rare platelet-specific antigen HPA-10bw allele found in Chinese mainland

FENG Ming-Liang1, SHEN Tong1, HUANG Hui1, SHEN Wei1, WANG Jian-Lian1,
LIU Da-Zhuang1, ZHAO Tong-Mao2

  

  1. 1. Shanghai Blood Center, Shanghai 200051, China;
    2. National Institutes of Health, Bethesda, MD 20892, USA

  • Received:2006-06-01 Revised:2006-07-20 Online:2007-02-10 Published:2007-02-10
  • Contact: Dazhuang Liu

Abstract:

A total of 1,000 Chinese blood donors were typed for human platelet antigens (HPA) using a sequence specific primers -polymerase chain reaction (PCR-SSP) based HPA genotyping method. An individual with a rare HPA-10w(a+b+) genotype was found. In order to confirm the typing results, a fragment of HPA-10 gene was amplified by PCR and then sequenced. Sequencing data showed that a single G to A substitution at nucleotide 263 occurred, resulting in amino acid change from Arg(CGA) to Gln(CAA) at position 62 of GPⅢa protein. The substitution generated antigenic specificity HPA-10bw. The detection of an HPA-10bw allele in the Chinese population suggests that this rare allele should be considered in platelet alloimmunization, such as neonatal alloimmune thrombocytopenia (NAIT), post-transfusion thrombocytopenic purpura (PTP) and post-transfusion refractoriness to platelets (PTR).