Vox Sanguinis (2013) REVIEW © 2013 International Society of Blood TransfusionDOI: 10.1111/vox.12085 Human platelet antigens – 2013

To date, 33 human platelet alloantigens (HPAs) have been identified on six func-tionally important platelet glycoprotein (GP) complexes and have been implicated in alloimmune platelet disorders including foetal and neonatal alloimmune thrombocytopenia (FNAIT), posttransfusion purpura (PTP) and multitransfusion platelet refractoriness (MPR). The greatest number of recognized HPA (20 of 33) resides on the GPIIb/IIIa complex, which serves as the receptor for ligands impor-tant in mediating haemostasis and inflammation. These include HPA-1a, the most commonly implicated HPA in FNAIT and PTP in Caucasian populations. Other platelet GP complexes, GPIb/V/IX, GPIa/IIa and CD109, express the remaining 13 HPAs. Of the recognized HPAs, 12 occur as six serologically and genetically defined biallelic ‘systems ’ where the –a form designates the higher frequency allele and the –b form, the lower. Twenty-one other HPAs are low-frequency or rare antigens for which postulated higher frequency –a alleles have not yet been identified as antibody specificities. In addition to the HPA markers, platelets also express ABO and human leucocyte antigen (HLA) antigens; antibodies directed at the former are occasionally important in FNAIT, and to the latter, in MPR. Key words: neonatal alloimmune thrombocytopenia, platelet antigens, platelet refractoriness