Blood group A and B antigens are strongly expressed on platelets of some individuals

  • Brian R. Curtis
    From the Blood Research Institute, The Blood Center of Southeastern Wisconsin, and the Departments of Medicine, Pathology, and Biostatistics of the Medical College of Wisconsin, Milwaukee, WI.
  • Jennifer T. Edwards
    From the Blood Research Institute, The Blood Center of Southeastern Wisconsin, and the Departments of Medicine, Pathology, and Biostatistics of the Medical College of Wisconsin, Milwaukee, WI.
  • Martin J. Hessner
    From the Blood Research Institute, The Blood Center of Southeastern Wisconsin, and the Departments of Medicine, Pathology, and Biostatistics of the Medical College of Wisconsin, Milwaukee, WI.
  • John P. Klein
    From the Blood Research Institute, The Blood Center of Southeastern Wisconsin, and the Departments of Medicine, Pathology, and Biostatistics of the Medical College of Wisconsin, Milwaukee, WI.
  • Richard H. Aster
    From the Blood Research Institute, The Blood Center of Southeastern Wisconsin, and the Departments of Medicine, Pathology, and Biostatistics of the Medical College of Wisconsin, Milwaukee, WI.

書誌事項

公開日
2000-08-15
DOI
  • 10.1182/blood.v96.4.1574
公開者
American Society of Hematology

この論文をさがす

説明

<jats:title>Abstract</jats:title><jats:p>It is widely thought that expression of ABH antigens on platelets is insufficient to materially affect the survival of ABH-incompatible platelets in transfusion recipients, but anecdotal reports of poor survival of A and B mismatched platelets suggest that this is not always the case. The A and B antigen expression on platelets of 100 group A1 and group B blood donors was measured, and 7% and 4%, respectively, had platelets whose A and B antigen levels consistently exceeded the mean plus 2 SD. On the basis of flow cytometric and statistical analysis, donors whose platelets contained higher than normal levels of A antigen were subdivided into 2 groups, designated Type I and Type II (“high expressers”). Serum A1- and B-glycosyltransferase levels of A and B high expressers were significantly higher than those of group A1 and B individuals with normal expression. H antigen levels were low on the red cells of high expressers, indicating that the anomaly affects other cell lineages. Immunochemical studies demonstrated high levels of A antigen on various glycoproteins (GPs) from high-expresser platelets, especially GPIIb and PECAM (CD31). The A1 Type II high-expresser phenotype was inherited as an autosomal dominant trait in one family. The sequences of exons 5, 6, and 7 of the A1-transferase gene of one Type II A1 high expresser and exon 7 from 3 other genes were identical to the reported normal sequences. Further studies are needed to define the molecular basis for the high-expresser trait and to characterize its clinical implications.</jats:p>

収録刊行物

  • Blood

    Blood 96 (4), 1574-1581, 2000-08-15

    American Society of Hematology

被引用文献 (3)*注記

もっと見る

詳細情報 詳細情報について

問題の指摘

ページトップへ