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作 者:陈青[1] 李平[2] 陆乐[2] 肖建宇[1] 王树亚 黄成垠[1] 姚根宏[2]
机构地区:[1]江苏省血液中心,南京2100422 [2]南京大学医学院附属鼓楼医院输血科
出 处:《临床血液学杂志(输血与检验)》2015年第1期91-93,共3页Journal of Clinical Hematology(Blood Transfusion & Laboratory Medicine)
基 金:江苏省科教兴卫工程医学重点人才(No:RC2011088);江苏省第4期333高层次人才培养工程;2010年度江苏省卫生国际交流支撑计划项目资助
摘 要:目的:应用分子生物学方法鉴定急性白血病患者ABO血型抗原,确定患者ABO血型正反定型不符的原因。方法:选取临床正反定型不一致白血病患者,常规血清学ABO血型正反定型;直接和间接抗人球蛋白试验检测不规则抗体;吸收放散法鉴定弱血型抗原;PCR方法扩增ABO基因的7个外显子及侧翼内含子,扩增产物进行测序及序列分析。结果:患者正定型为AB亚型,反定型为AB型;直抗和间抗为阴性;吸收放散试验证明红细胞上存在弱A和B抗原;ABO基因扩增产物测序结果表明其基因型为ABO*A102/B101。结论:该白血病患者经分子生物学方法确定为正常AB型,其血型抗原减弱由白血病所致。基因分型法可以正确区分血型抗原减弱或亚型。Objective:To indentify ABO blood group antigen by genotyping,and explore the mechanism of ABO discrepancy in a patient due to acute leukemia.Method:A acute myeloid leukemia patient with ABO typing discrepancy was selected.Routine serological test was carried out to analyze ABO blood group.Both direct and indirect anti-globulin tests were performed to screen irregular antibodies.The presence of the blood group determinants on the red blood cells were determined by adsorption-elution test.Exons 1-7and adjacent introns of the ABO gene were amplified by PCR and sequenced.Result:ABO forward typing indicated that the patient was AB subgroup.However the reverse typing defined AB.Direct and indirect anti-globulin tests were negative.The RBCs could adsorb anti-A and anti-B,which were able to be eluted subsequently.ABO genotyping was ABO*A102/B101.Conclusion:The leukemia patient with ABO discrepancy by serological test was defined as AB by molecular genetic analysis.The suppressed expressions of A and B antigens on RBCs were due to acute myeloid leukemia.The genotyping could be used to differentiate the subgroup and suppressed expressions of blood group antigens.
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