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本文引用的文献

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International society of blood transfusion working party on red cell immunogenetics and terminology: report of the Seoul and London meetings.国际输血协会红细胞免疫遗传学与术语工作组:首尔及伦敦会议报告
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2
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Clin Lab. 2016 Nov 1;62(11):2227-2232. doi: 10.7754/Clin.Lab.2016.160432.
3
Distribution of DI*A and DI*B Allele Frequencies and Comparisons among Central Thai and Other Populations.泰国中部人群与其他人群中DI*A和DI*B等位基因频率的分布及比较。
PLoS One. 2016 Oct 20;11(10):e0165134. doi: 10.1371/journal.pone.0165134. eCollection 2016.
4
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Red blood cell antigen genotype analysis for 9087 Asian, Asian American, and Native American blood donors.对9087名亚洲、亚裔美国和美国原住民献血者进行红细胞抗原基因型分析。
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Red blood cell alloimmunization in sickle cell disease: listen to your ancestors.镰状细胞病中的红细胞同种免疫:倾听你的祖先的意见。
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The Diego blood group system: a review.迭戈血型系统综述
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Improved allele-specific PCR technique for Kidd blood group genotyping.改良的 Kidd 血型基因分型等位基因特异性 PCR 技术。
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通过多重PCR进行红细胞基因分型可为依赖输血的泰国患者鉴定抗原匹配的血液单位。

Red Cell Genotyping by Multiplex PCR Identifies Antigen-Matched Blood Units for Transfusion-Dependent Thai Patients.

作者信息

Intharanut Kamphon, Bejrachandra Sasitorn, Nathalang Siriporn, Leetrakool Nipapan, Nathalang Oytip

机构信息

Graduate Program in Biomedical Sciences, Faculty of Allied Health Sciences, Thammasat University, Pathumtani, Thailand.

National Blood Centre, Thai Red Cross Society, Bangkok, Thailand.

出版信息

Transfus Med Hemother. 2017 Sep;44(5):358-364. doi: 10.1159/000471886. Epub 2017 May 12.

DOI:10.1159/000471886
PMID:29070981
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5649308/
Abstract

BACKGROUND

Antigen-negative red cell transfusion is required for transfusion-dependent patients. We developed multiplex PCR for red cell genotyping and calculated the possibility of finding compatible predicted phenotypes in Thai blood donor populations according to red cell alloantibodies found among Thai patients.

METHODS

600 DNA samples obtained from unrelated healthy central and northern Thai blood donors were tested with the newly developed multiplex PCR for , , , , , , and , and allele detections. Additionally, the possibility of finding compatible predicted phenotypes in two Thai blood donor populations was calculated to estimate the minimal number of tests needed to provide compatible blood.

RESULTS

The validity of multiplex PCR using known DNA controls and the phenotyping and genotyping results obtained by serological and PCR-SSP techniques were in agreement. The possibility of finding at least one compatible blood unit for patients with multiple antibodies was comparable in Thai populations.

CONCLUSIONS

The multiplex PCR for red cell genotyping simultaneously interprets 7 alleles and 1 hybrid GP group. Similar strategies can be applied in other populations depending on alloantibody frequencies in transfusion-dependent patients, especially in a country with limited resources.

摘要

背景

依赖输血的患者需要输注抗原阴性的红细胞。我们开发了用于红细胞基因分型的多重聚合酶链反应(PCR),并根据泰国患者中发现的红细胞同种抗体,计算了在泰国献血人群中找到相容预测表型的可能性。

方法

从泰国中部和北部无亲缘关系的健康献血者中获取600份DNA样本,使用新开发的多重PCR对 、 、 、 、 、 以及 和 等位基因进行检测。此外,计算了在两个泰国献血人群中找到相容预测表型的可能性,以估计提供相容血液所需的最少检测次数。

结果

使用已知DNA对照的多重PCR的有效性与通过血清学和PCR-序列特异性引物(PCR-SSP)技术获得的表型和基因分型结果一致。在泰国人群中,为具有多种抗体的患者找到至少一个相容血液单位的可能性相当。

结论

用于红细胞基因分型的多重PCR可同时解读7个等位基因和1个杂合糖蛋白(GP)组。根据依赖输血患者的同种抗体频率,类似策略可应用于其他人群,尤其是在资源有限的国家。