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Genotyping for human platelet alloantigen polymorphisms: applications in the diagnosis of alloimmune platelet disorders. Semin Thromb Hemost 2008 Sep;34(6):539-48

Date

12/17/2008

Pubmed ID

19085653

DOI

10.1055/s-0028-1103365

Scopus ID

2-s2.0-57149108912 (requires institutional sign-in at Scopus site)   33 Citations

Abstract

Molecular typing for platelet allelic polymorphisms was first made possible by discovery of the HPA-1a/1b single nucleotide polymorphism in 1989. Since then, six other biallelic human platelet antigen (HPA) systems have been determined and can be typed using genomic DNA. The introduction of polymerase chain reaction enabled development of several different assays including polymerase chain reaction-sequence-specific primer, melting curve analysis by LightCycler, and 5'-nuclease assays. More recently, multiplex polymerase chain reaction has allowed for the development of high-throughput assays for genotyping large numbers of patients and blood donors for not only platelet gene polymorphisms but also for those of other blood cell genes. Platelet genotyping is a valuable tool in confirming platelet antigen specificities of alloantibodies detected in patient sera to complement the clinical history in the diagnosis of alloimmune platelet disorders such as fetal and neonatal alloimmune thrombocytopenia (FNAIT), posttransfusion purpura, and multiplatelet transfusion refractoriness. In addition, it has made possible prenatal platelet typing of the fetus in suspected cases of FNAIT and large-scale blood donor typing for provision of antigen-negative platelets to transfuse highly alloimmunized patients. Platelet genotyping may also someday prove important as an aid in determining the relative risk of patients for various thrombotic disorders.

Author List

Curtis BR

Author

Brian Curtis PhD Director in the Platelet & Neutrophil Immunology Laboratory department at BloodCenter of Wisconsin




MESH terms used to index this publication - Major topics in bold

Antigens, Human Platelet
Autoantibodies
Blood Platelets
DNA Mutational Analysis
Genotype
Humans
Isoantibodies
Platelet Transfusion
Polymorphism, Genetic
Polymorphism, Restriction Fragment Length
Purpura, Thrombocytopenic, Idiopathic
Thrombocytopenia, Neonatal Alloimmune