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Objective To investigate the serological and molecular identification of 2 rare B( A) blood groups. Methods The ABO blood groups of 2 samples from blood donors were detected by routine serological method. The genotype features was identified by PCR-sequence specific primer (PCR-SSP) and direct sequence analysis. Results The serological results for the 2 blood donors showed the characteristics of B(A) phenotype. The sample 1 was genotyped as BO2 subtype by PCR-SSP and direct sequencing showed B alleles in exon 7, presented nt640 A＞G mutation which was confirmed to be B(A)04/O02 genotype.The sample 2 was genotyped as BO1 sub-type by PCR-SSP and direct sequencing showed B alleles presented nt700 C＞G mutation in exon 7 which was confirmed to be B(A)02/O01 genotype. Conclusion The phenotype of the two samples should be B ( A ) and the genotypes should be rare B(A)04/O02 and B(A)02/O01.
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Objective:To study on significance of ABO genotyping.Methods:To use the methods of polymerase chain reaction sequence specific primers(PCR SSP) for genotyping of ABO blood group and observation ABO gene polymorphism as well as identification of doubt sample.Results:The reliability of the genotyping for ABO blood group was proved by testing DNA samples previously known genotypes.The results of genotyping for 104 healthy and unrelated HAN individuals were correspond with serological phenotypes.The method of ABO genotyping was applied for clinical pre transfusion ABO typing,pre delivery fetal ABO typing,parenting test and subgrouptyping.Conclusion:The method of ABO genotyping may correct typing for doubt sample of ABO serological typing.
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Objectives:The purpose of this study is to provide a HLA B locus genotyping method which is expected to compensate the unsatisfactory serology B locus typing and to explore the distribution of B22 subtypes.Methods:Taking standard cell lines provided by the XIIth International HLA Workshop as reference,the authors established the PCR SSP method for HLA B genotyping.By this method,the HLA B alleles of leukemia patients were typed and 57 individuals previously identified as HLA B22 by serologic typing were genotyped.Results:The results of B locus genotyping of 104 cell lines by PCR SSP and that of reported were completely concordant .Unambiguous results of 17 leukemia patients and their relations were gotten except one discordant from serology which was thought as mistaken serotyping .Out of 57 samples ,55 were confirmed to bear B54 or B55 or B56 allele,respectively ,with B54 being the most common allelic form,and another showed a unique amplifying pattern which was different from any known HLA B22 alleles so far reported, suggesting a new allele or "mismatched ”DNA double strands which needed further study .Conclusions:PCR SSP was proven to be a practical genotyping method for B locus because of its simplicity, rapidity ,accuracy and unvariability with changes of health.