Maxa, a new low-frequency platelet-specific antigen localized on glycoprotein IIb, is associated with neonatal alloimmune thrombocytopenia

P. Noris, S. Simsek, L. G. De Bruijne-Admiraal, L. Porcelijn, E. Huiskes, G. J. Van der Vlist, E. F. Van Leeuwen, C. E. Van der Schoot, A. E G K Von dem Borne

Research output: Contribution to journalArticlepeer-review

Abstract

We have identified a new platelet-specific alloantigen, Maxa, responsible for a typical case of neonatal alloimmune thrombocytopenic purpura. The maternal serum reacted strongly with paternal platelets in the platelet immunofluorescence test, whereas platelet alloantigen typing showed that no known human platelet antigen (HPA)-system was involved. In the monoclonal antibody (MoAb)-specific immobilization of platelet antigens (MAIPA) assay, the new antigen was located on the platelet membrane glycoprotein (GP) IIb- IIIa complex, but immunoprecipitation and immunoblot experiments to further localize the antigen failed. However, in the MAIPA assay, the binding of the anti-Maxa antibodies from the maternal serum was blocked by two anti-GPIIb MoAbs. Thus, the antigen appeared to be located on GPIIb. Analysis of the family lead to the identification of six additional Maxa+ individuals. Three of these six individuals and the father were tested in the platelet aggregation test and were found to be normal. In the analysis of normal donors, three of 500 were typed positive for the new platelet-specific antigen, indicating a phenotype frequency of 0.6% in the normal population. Platelet RNA was isolated from the newborn's Maxa+ father and from a healthy donor phenotyped as Maxa-, reverse-transcribed, and the entire GPIIb coding region was amplified by polymerase chain reaction. Subsequent nucleotide sequence analysis showed a single G → A substitution at position 2,603, predicting a valine → methionine amino acid substitution at position 837 of the mature glycoprotein. This mutation abolished a BsiYI restriction site at the cDNA level and a BstNI restriction site at genomic DNA level, respectively. The genetic association between the new antigen and this point mutation was confirmed by allele-specific restriction analysis on cDNA and on genomic DNA, as well as by allele-specific primer amplification on genomic DNA. The new mutation is 19 bp upstream of the mutation underlying the HPA-3 system. Therefore, we also evaluated the association between Max and the HPA- 3 polymorphism. So far, all Maxa+ individuals were also found to be HPA- 3b, whereas 50 HPA-3a individuals were all Maxa-. This may indicate that Maxa is a variant of the HPA-3b allele.

Original languageEnglish
Pages (from-to)1019-1026
Number of pages8
JournalBlood
Volume86
Issue number3
Publication statusPublished - 1995

ASJC Scopus subject areas

  • Hematology

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