[对一名合并 FUT1 和 ABO 双血型基因变异导致准孟买血型和 A2 亚型血型的献血者的遗传分析及文献综述]。

Ziyi He, Yingming Hu, Menghui Bei, Xiaomei Jie, Xianguo Xu
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Adsorption-elution test was conducted to detect trace antibodies in the blood donor's plasma to trace the A, B and H antigens on the red blood cell surface. Sanger sequencing was carried out to analyze the sequences of the FUT1 and ABO genes. Using keywords such as \"para-Bombay\" \"FUT1*01W.37\" and \"FUT1*01W.23\" both in Chinese and English, relevant literature on para-Bombay blood type subjects carrying FUT1*01W.37 and FUT1*01W.23 alleles was retrieved from the CNKI, Wanfang Data Knowledge Service Platform, and PubMed databases, and the retrieval time was set as from the establishment of database to December 2022. 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引用次数: 0

摘要

目的研究一名FUT1和ABO血型基因变异导致副孟买血型和A2亚型的自愿献血者的血清学和分子遗传学特征,并回顾携带FUT101W.37和FUT101W.23等位基因的副孟买血型的相关文献:选取 2023 年 8 月在东莞市中心血站参加自愿无偿献血的准孟买血和 A2 亚型献血者作为研究对象。通过血清学检测确定献血者的 ABO 血型、路易斯血型抗原和意外血清抗体。通过吸附洗脱试验检测献血者血浆中的微量抗体,以追踪红细胞表面的 A、B 和 H 抗原。通过桑格测序分析 FUT1 和 ABO 基因的序列。以 "para-Bombay""FUT1*01W.37 "和 "FUT1*01W.23 "为中英文关键词,从CNKI、万方数据知识服务平台和PubMed数据库中检索携带FUT1*01W.37和FUT1*01W.23等位基因的para-Bombay血型受试者的相关文献,检索时间定为数据库建立至2022年12月。本研究已获得东莞市中心血站伦理委员会批准(编号:2022005),并获得献血者的知情同意:结果:对献血者进行血清学检测后发现,ABO血型正反分型结果不一致,红细胞表面H抗原阴性,Lewis血型为Le(a-b+)分泌型,血浆中存在意外的抗-H抗体,疑似副孟买型。吸收洗脱试验显示献血者的血型为准孟买型和 A 亚型。桑格(Sanger)测序显示,该献血者携带同型FUT1*(c.35T+c.803A)/(c.35T+c.803A)变异,其中FUT1*(c.35T+c.803A)等位基因含有国际输血协会(ISBT)FUT1基因变异数据库未记录的双核苷酸变异,与FUT101W的弱功能等位基因相似。37(c.803G>A)。ABO基因型为杂合ABOA2.05/O.01.02。结合血清学和基因检测结果,确定献血者的血型为准孟买血和 A2 亚型。通过查阅文献,发现一名来自青岛的孕妇携带 FUT1*01W.37 等位基因,2 人携带杂合子 FUT1*01W.23 等位基因:本研究发现了一名副孟买血型和 ABO 亚型并存的献血者。根据红细胞表面抗原的特征,FUT1*01W.37 被归类为 FUT1 空等位基因。
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[Genetic analysis of a blood donor with combined FUT1 and ABO dual blood group gene variants resulting in para-Bombay and A2 subtype blood types and a literature review].

Objective: To investigate the serological and molecular genetic characteristics of a voluntary blood donor with combined FUT1 and ABO blood group gene variants causing para-Bombay and A2 subtype, and to review relevant literature on para-Bombay blood types carrying alleles such as FUT101W.37 and FUT101W.23.

Methods: A blood donor with para-Bombay and A2 subtype who participated in voluntary blood donation at the Dongguan Blood Center in August 2023 was selected as the study subject. Serological tests were performed to identify the ABO blood group, Lewis blood group antigens, and unexpected serum antibodies in the donor. Adsorption-elution test was conducted to detect trace antibodies in the blood donor's plasma to trace the A, B and H antigens on the red blood cell surface. Sanger sequencing was carried out to analyze the sequences of the FUT1 and ABO genes. Using keywords such as "para-Bombay" "FUT1*01W.37" and "FUT1*01W.23" both in Chinese and English, relevant literature on para-Bombay blood type subjects carrying FUT1*01W.37 and FUT1*01W.23 alleles was retrieved from the CNKI, Wanfang Data Knowledge Service Platform, and PubMed databases, and the retrieval time was set as from the establishment of database to December 2022. This study has been approved by the Ethics Committee of Dongguan Blood Center (No. 2022005), and informed consent of blood donation was obtained from the blood donor.

Results: Serological testing of the blood donor revealed inconsistent results between forward and reverse ABO blood typing, negative H antigen on the red blood cell surface, Le(a-b+) secretor type for Lewis blood group, and unexpected anti-H antibodies in the plasma, indicating a suspected para-Bombay type. Absorption-elution test suggested the blood type of the blood donor to be para-Bombay and A subtype. Sanger sequencing showed that the donor has harbored homozygous FUT1*(c.35T+c.803A)/(c.35T+c.803A) variant, with the FUT1*(c.35T+c.803A) allele containing a dual nucleotide variant unrecorded by the International Society of Blood Transfusion (ISBT) FUT1 gene variant database, which was similar to the weakly functional allele of FUT101W. 37(c.803G>A) as recorded by the ISBT database. The ABO genotype was heterozygous ABOA2.05/O.01.02. Combining the results of serological and genetic testing, the blood type of the blood donor was determined to be para-Bombay and A2 subtypes. Literature review has identified a pregnant women from Qingdao carrying the FUT1*01W.37 allele and 2 individuals carrying a heterozygous FUT1*01W.23 allele.

Conclusion: This study has discovered a blood donor with coexisting para-Bombay and ABO subtype blood groups. Based on the characteristics of red blood cell surface antigens, the FUT1*01W.37 as classified as an FUT1 null allele.

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来源期刊
中华医学遗传学杂志
中华医学遗传学杂志 Medicine-Medicine (all)
CiteScore
0.50
自引率
0.00%
发文量
9521
期刊介绍: Chinese Journal of Medical Genetics is a medical journal, founded in 1984, under the supervision of the China Association for Science and Technology, sponsored by the Chinese Medical Association (hosted by Sichuan University), and is now a monthly magazine, which attaches importance to academic orientation, adheres to the scientific, scholarly, advanced, and innovative, and has a certain degree of influence in the industry. Chinese Journal of Medical Genetics is a journal of Peking University, and is now included in Peking University Journal (Chinese Journal of Humanities and Social Sciences), CSCD Source Journals of Chinese Science Citation Database (with extended version), Statistical Source Journals (China Science and Technology Dissertation Outstanding Journals), Zhi.com (in Chinese), Wipu (in Chinese), Wanfang (in Chinese), CA Chemical Abstracts (U.S.), JST (Japan Science and Technology Science and Technology), and JST (Japan Science and Technology Science and Technology Research Center). ), JST (Japan Science and Technology Agency), Pж (AJ) Abstracts Journal (Russia), Copernicus Index (Poland), Cambridge Scientific Abstracts, Abstracts and Citation Database, Abstracts Magazine, Medical Abstracts, and so on.
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