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Variant genotypes associated with reduced expression of RhCE antigens among Brazilian blood donors.
Dezan, Marcia Regina; Oliveira, Valéria B; Conrado, Marina C A V; da Rocha, Mateus Cardoso; Luz, Fabio; Gallucci, Antonio; Pereira, Alexandre C; Krieger, José E; Rocha, Vanderson; Mendrone-Junior, Alfredo; Dinardo, Carla Luana.
Afiliação
  • Dezan MR; Fundação Pró-Sangue Hemocentro de São Paulo, São Paulo, Brazil.
  • Oliveira VB; Fundação Pró-Sangue Hemocentro de São Paulo, São Paulo, Brazil.
  • Conrado MCAV; Fundação Pró-Sangue Hemocentro de São Paulo, São Paulo, Brazil.
  • da Rocha MC; Fundação Pró-Sangue Hemocentro de São Paulo, São Paulo, Brazil.
  • Luz F; Fundação Pró-Sangue Hemocentro de São Paulo, São Paulo, Brazil.
  • Gallucci A; Fundação Pró-Sangue Hemocentro de São Paulo, São Paulo, Brazil.
  • Pereira AC; Laboratory of Genetics and Molecular Cardiology, Heart Institute, University of São Paulo, São Paulo, Brazil.
  • Krieger JE; Laboratory of Genetics and Molecular Cardiology, Heart Institute, University of São Paulo, São Paulo, Brazil.
  • Rocha V; Fundação Pró-Sangue Hemocentro de São Paulo, São Paulo, Brazil.
  • Mendrone-Junior A; Department of Hematology, Churchill Hospital, NHS BT, Oxford University, Oxford, UK.
  • Dinardo CL; Discipline of Hematology, University of São Paulo School of Medicine, São Paulo, Brazil.
Transfusion ; 61(6): 1923-1931, 2021 06.
Article em En | MEDLINE | ID: mdl-33687082
ABSTRACT

BACKGROUND:

The genetic diversity of the RHCE gene locus has been explored in diverse populations of different racial backgrounds. Data referring to the diversity of RHCE encoding weakened expression of C, c, E, and e in multiethnic populations is still incomplete.

METHODS:

Samples from Brazilian blood donors presenting reduced expression of C, c, E, or e on gel method were selected for the study. All exons and flanking introns of RHCE were genotyped though direct Sanger sequencing for the included donors.

RESULTS:

Sixty-six donors were included 23 with weak C, 22 with weak c, 6 with weak E, 14 with weak e, and 1 with weak c and E. Among the samples with weak C, the following altered RH*C were encountered RHCE*CeMA (n = 3), RHCE*Ce941C (n = 1), and RHCE*CeVA (n = 1). RHD*D-CE(4-7)-D was detected in six cases, RHCE*CE was presumably present in five cases, and seven cases were unexplained. Two altered alleles underlay the weak c phenotype RHCE*ceJAL (n = 20) and RHCE*ce340T (n = 2), and two altered RHCE justified weak e RHCE*ceMO (n = 6) and RHCE*ceJAL (n = 8). Three variant RHCE were associated with weak E RHCE*cEJU (n = 4), RHCE*cE382C (n = 1), and RHCE*cEIV (n = 1). The RHCE*cE905A justified one case of weak c and E.

CONCLUSION:

We describe the distribution of RHCE variants found in association with weak expression of C, c, E, and e in blood donors of multiethnic origin, which differs in comparison to that previously reported for people of African or Caucasian descent.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sistema do Grupo Sanguíneo Rh-Hr / Doadores de Sangue Tipo de estudo: Risk_factors_studies Limite: Humans País/Região como assunto: America do sul / Brasil Idioma: En Revista: Transfusion Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Brasil

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sistema do Grupo Sanguíneo Rh-Hr / Doadores de Sangue Tipo de estudo: Risk_factors_studies Limite: Humans País/Região como assunto: America do sul / Brasil Idioma: En Revista: Transfusion Ano de publicação: 2021 Tipo de documento: Article País de afiliação: Brasil