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Human platelet alloantigens (HPAs): PCR-SSP genotyping of a UK population for 15 HPA alleles
Journal article   Peer reviewed

Human platelet alloantigens (HPAs): PCR-SSP genotyping of a UK population for 15 HPA alleles

D.C. Jones, M. Bunce, S.V. Fuggle, N.T. Young and S.E. Marshall
European Journal of Immunogenetics, Vol.30(6), pp.415-419
2003
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Abstract

Alloimmunization to human platelet alloantigens (HPAs) is responsible for neonatal alloimmune thrombocytopenia (NAIT), post-transfusional purpura (PTP) and platelet transfusion refractoriness. HPAs may also have a role as histocompatibility antigens in transplantation as well as associations with cardiac disease. We have developed a polymerase chain reaction-sequence- specific primer (PCR-SSP) assay capable of detecting 15 HPA allelic variants. As part of the validation of the assay, 134 UK renal donors were genotyped to determine HPA allele frequencies in the UK population. The HPA allele frequencies obtained are consistent with those of the other European studies: GP1A*1 (HPA-5a) and GP1A*2 (HPA-5b), 0.914 and 0.086, respectively; GP1BA*1 (HPA-2a) and GP1BA*2 (HPA-2b), 0.925 and 0.075; GP2B*1 (HPA-3a) and GP2B*2 (HPA-3b), 0.627 and 0.373; GP3A*1 (HPA-1a) and GP3A*2 (HPA-1b), 0.840 and 0.161. The rare alleles GP2B*3 (HPA-9bw) and GP3A*3 to *8 (HPA-4b, -6b, -7bw, -8bw, -10bw and -11bw, respectively) were all absent. This comprehensive HPA genotyping assay allows rapid, accurate and reproducible results at low cost.

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Collaboration types
Domestic collaboration
Citation topics
1 Clinical & Life Sciences
1.103 Blood Disorders
1.103.1225 Immune Thrombocytopenia
Web Of Science research areas
Genetics & Heredity
Immunology
ESI research areas
Immunology
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