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(Referência obtida automaticamente do Web of Science, por meio da informação sobre o financiamento pela FAPESP e o número do processo correspondente, incluída na publicação pelos autores.)

RHD alleles in Brazilian blood donors with weak D or D-negative phenotypes

Texto completo
Autor(es):
Cruz, B. R. [1] ; Chiba, A. K. [1] ; Moritz, E. [1] ; Bordin, J. O. [1]
Número total de Autores: 4
Afiliação do(s) autor(es):
[1] Univ Fed Sao Paulo, Disciplina Hematol & Hemoterapia, BR-04023092 Sao Paulo - Brazil
Número total de Afiliações: 1
Tipo de documento: Artigo Científico
Fonte: Transfusion Medicine; v. 22, n. 2, p. 84-89, APR 2012.
Citações Web of Science: 23
Resumo

The RHD gene is highly polymorphic and the existence of a large number of alleles results in RhD variant phenotypes. RHD genotyping has been used to distinguish normal D antigen from D variants due to limitations of serologic methods. The purpose of this study was to determine the phenotypic frequency of RhD and RhCE antigens and to investigate the RHD alleles present in samples with the weak D or D- phenotypes from Brazilian blood donors. A total of 2007 donors were phenotyped for D, C, c, E and e antigens. Samples phenotyped as D- were genotyped by polymerase chain reaction-sequence specific primers, and exon 10 and intron 4 of the RHD gene were analysed. D- samples containing the RHD gene or samples considered weak D were further characterised using genotyping platform or nucleotide sequencing. Using serologic methods we found that 87.3% of the donors were D+, 11.9% D- and 0.8% weak D. The frequency of RHD gene in D- individuals was 9.2%. Five RHD alleles from phenotypically D- donors were characterised in six molecular backgrounds: RHD, RHD-CE-Ds, RHD-CE-(2-9)-D, RHD/RHD, RHD/RHD-CE-Ds and RHD-CE(2)-D. The most common weak D antigens types found were 1, 3, 4.0/4.1 and 4.2, whereas the most prevalent weak D type was 4.2 (or DAR). The RHD genotyping proved to be a necessary tool to characterise RHD alleles in donors phenotyped as D- or weak D to increase the transfusion safety in highly racial mixed population. (AU)

Processo FAPESP: 05/55237-9 - Aspectos clínicos e moleculares de antígenos e anticorpos de células sanguíneas
Beneficiário:Jose Orlando Bordin
Modalidade de apoio: Auxílio à Pesquisa - Temático