...
首页> 外文期刊>Transfusion medicine and hemotherapy: offizielles Organ der Deutschen Gesellschaft fur? Transfusionsmedizin und Immunham?atologie >Towards a Regional Registry of Extended Typed Blood Donors: Molecular Typing for Blood Group, Platelet and Granulocyte Antigens
【24h】

Towards a Regional Registry of Extended Typed Blood Donors: Molecular Typing for Blood Group, Platelet and Granulocyte Antigens

机译:迈向延长类型献血者的区域登记处:血型,血小板和粒细胞抗原的分子键入

获取原文
获取原文并翻译 | 示例

摘要

Background: The provision of compatible blood products to patients is the most essential task of transfusion medicine. Besides ABO and Rh, a number of additional blood group antigens often have to be considered for the blood supply of immunized or chronically transfused patients. It also applies for platelet antigens (HPA) and neutrophil antigens (HNA) for patients receiving platelet or granulocyte concentrates. Here, we describe the molecular screening for a number of blood group, HPA, and HNA alleles. Based on the screening results we are building up a regional blood donor registry to provide extended matched blood products on demand. Methods: We developed and validated TaqMan? PCR and PCR-SSP methods for genetic markers defining 37 clinically relevant blood group antigens (beyond ABO and Rh), 10 HPA, and 11 HNA. Furthermore, we describe a feasible method for fast molecular screening of the HNA-2~(null)phenotype. All data were statistically evaluated regarding genotype distribution. Allele frequencies were compared to ExAC data from non-Finnish Europeans. Results: Up to now more than 2,000 non-selected regular blood donors in south-west Germany have been screened for blood group, HPA, and HNA alleles. The screening results were confirmed by serology and PCR-SSP methods for selected numbers of samples. The allele frequencies were similar to non-finnish Europeans in the ExAC database except for the alleles encoding the S, HPA-3b and HNA-4b antigens, with significantly lower prevalence in our cohort, as well as the LU14 and the HNA-3b antigens, with a higher frequency compared to the ExAC data. We identified 71 donors with rare blood groups such as Lu(a+b-), Kp(a+b-), Fy(a-b-) and Vel-, and 169 donors with less prevalent HPA or HNA types. Conclusion: Molecular screening for blood group alleles by using TaqMan? PCR is an effective and reliable high-throughput method for establishing a rare donor registry.
机译:背景:向患者提供兼容的血液产品是输血药物最重要的任务。除了ABO和RH之外,还必须考虑许多额外的血液组抗原用于免疫或长次输血患者的血液供应。它还适用于接受血小板或粒细胞浓缩物的患者的血小板抗原(HPA)和中性粒细胞抗原(HNA)。在这里,我们描述了许多血基,HPA和HNA等位基因的分子筛。根据筛选结果,我们建立了一个区域献血者注册机构,以提供延长匹配的血液产品。方法:我们开发和验证了Taqman吗? PCR和PCR-SSP用于遗传标记的方法,用于定义37个临床相关的血型抗原(超越ABO和RH),10 HPA和11个HNA。此外,我们描述了一种可行的方法,用于快速分子筛选HNA-2〜(零)表型。关于基因型分布的统计评估所有数据。将等位基因频率与非芬兰欧洲人的exac数据进行比较。结果:德国西南部的达到现在超过2,000多个未选择的普通献血者已被筛查血型,HPA和HNA等位基因。通过血清学和PCR-SSP方法确认筛选结果,用于选定数量的样品。除了编码S,HPA-3B和HNA-4B抗原的等位基因外,等位基因频率与EXAC数据库中的非芬兰欧洲人类似,在我们的队列中具有显着较低的患病率,以及LU14和HNA-3B抗原,与EXAC数据相比,频率更高。我们鉴定了71种含有稀有血型的供体,如Lu(A + B-),KP(A + B + B +),FY(A-B-)和VEL-,169个供体,具有较少普遍的HPA或HNA类型。结论:使用Taqman对血型等位基因的分子筛选吗? PCR是一种用于建立罕见捐助者登记处的有效可靠的高通量方法。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号