机构:
Univ W England, Fac Sci Appl, Biomed Res Ctr, Bristol Genom Res Inst, Bristol BS16 1QY, Avon, EnglandUniv W England, Fac Sci Appl, Biomed Res Ctr, Bristol Genom Res Inst, Bristol BS16 1QY, Avon, England
Avent, Neil D.
[1
]
机构:
[1] Univ W England, Fac Sci Appl, Biomed Res Ctr, Bristol Genom Res Inst, Bristol BS16 1QY, Avon, England
blood group;
polymorphism;
genotyping;
SNP;
DNA chips;
D O I:
10.1016/j.tracli.2007.04.011
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Determination of predicted blood group phenotype by determination of genotype has been performed since the 1990s. This evolved due to the,roup antigen expression, which started in 1990 with ABO and RH systems rapid accrual of information surrounding the molecular basis of blood g and has now resulted in the molecular description of 28 of the 29 blood groups. Blood group genotyping is currently performed mostly for fetal blood group incompatibility and for assessment of multi-transfused patients. Both of these clinical scenarios are either dangerous or technically difficult, respectively to define serologically. With the simultaneous development of mass scale genotyping platforms it has now permitted the application of them to blood group genotype determination. In this paper, I describe some recently published work that has demonstrated that mass scale genotyping approaches are feasible. These approaches may lead to more effective management of blood stocks and patient cross-matching by reducing the dependence on serology during the time critical pre-transfusion phase. It is most probable that large scale studies, perhaps involving many European Union and North American based blood suppliers, may drive the introduction of this technology and convince red cell serologists that this approach may allow their work to be more focussed. (C) 2007 Elsevier Masson SAS. All rights reserved.