Prevalence of the HPA-18w to -21w alleles in the Chinese Han population

Int J Immunogenet. 2013 Apr;40(2):99-103. doi: 10.1111/j.1744-313X.2012.01142.x. Epub 2012 Aug 4.

Abstract

Recently, four new platelet alloantigen (HPA) systems HPA-18w to-21w were identified. However, genotyping for HPA-18w to -21w alleles was rarely reported. Here, we established a polymerase chain reaction sequence-based typing (PCR-SBT) method and investigated the distribution of HPA-18w to -21w alleles in the Chinese Han population. The specific primers of HPA-18w, -19w, -20w and -21w were designed, and the PCR products were bidirectionally sequenced. 855 randomly selected platelet donors were genotyped for HPA-18w to -21w with the PCR-SBT method. The results showed that all individuals were monomorphic for HPA-18w to HPA-20w with a/a homozygous frequency of 1.0 and absence of HPA-18bw to -20bw alleles. The frequencies of the HPA-21a/21a and HPA-21a/21b genotypes were 0.981(839/855) and 0.019(16/855), respectively. Seven mutations were confirmed on sequenced region separate from HPA polymorphisms, including ITGA2 (IVS17+48G>A and IVS17+72G>A), ITGA2B (IVS19-26C>G) and ITGB3 (IVS4+234C>T, IVS11-19 T>C, IVS11-104T>C and GT repeats from IVS11-131 to IVS11-109). These data will provide useful information for diagnosis, prevention and treatment of alloimmune thrombocytopaenia.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Antigens, Human Platelet / genetics*
  • Asian People / genetics*
  • Base Sequence
  • China
  • Gene Frequency
  • Genotype
  • Humans
  • Microsatellite Repeats / genetics
  • Molecular Sequence Data
  • Mutation
  • Polymorphism, Single Nucleotide
  • Sequence Analysis, DNA
  • Thrombocytopenia, Neonatal Alloimmune / diagnosis
  • Thrombocytopenia, Neonatal Alloimmune / genetics
  • Thrombocytopenia, Neonatal Alloimmune / therapy

Substances

  • Antigens, Human Platelet

Associated data

  • GENBANK/JN377425
  • GENBANK/JN377426
  • GENBANK/JQ964059