| Literature DB >> 20872565 |
Gláucia Andréia Soares Guelsin1, Ana Maria Sell, Lilian Castilho, Viviane Lika Masaki, Fabiano Cavalcante Melo, Margareth Naomi Hashimoto, Tatiana Takahashi Higa, Loide Souza Hirle, Jeane Eliete Laguila Visentainer.
Abstract
We evaluated the usefulness of blood group genotyping as a supplement to hemagglutination to determine the red blood cell (RBC) antigen profile of polytransfused patients with hematological diseases and renal failure. Seventy-nine patients were selected. They all received more than three units of blood and eight (10%) had already clinical significant alloantibodies occurring alone or in combination against Rh, K, Fya, and Di antigens. DNA was prepared from blood samples and RHCE*E/e, KEL*01/KEL*02, FY*01/FY*02 and JK*01/JK*02 alleles were determined by using PCR-RFLP. RHD*/RHD*Ψ and RHCE*C/c were tested using multiplex PCR. Discrepancies for Rh, Kell, Duffy, and Kidd systems were found between the phenotype and genotype-derived phenotype in 16 of the 38 chronically transfused patients. The genotypes of these patients were confirmed by DNA array analysis (HEA Beadchip(™); Bioarray Solutions, Warren, NJ). Genotyping was very important for the determination of the true blood groups of the polytransfused patients, helped in the identification of suspected alloantibodies and in the selection of antigen-negative RBCs for transfusion. J. Clin. Lab. Anal. 24:311-316, 2010.Entities:
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Year: 2010 PMID: 20872565 PMCID: PMC6647652 DOI: 10.1002/jcla.20407
Source DB: PubMed Journal: J Clin Lab Anal ISSN: 0887-8013 Impact factor: 2.352