[1]赵甜,张晨光,庞桂芝.新乡地区Rh阴性无偿献血者Rh表型分布及RhD变异型基因型分析[J].新乡医学院学报,2023,40(5):458-461.[doi:10.7683/xxyxyxb.2023.05.011]
 ZHAO Tian,ZHANG Chenguang,PANG Guizhi.Analysis of Rh phenotype distribution of Rh negative unpaid blood donors and RhD variant genotype in Xinxiang area[J].Journal of Xinxiang Medical University,2023,40(5):458-461.[doi:10.7683/xxyxyxb.2023.05.011]
点击复制

新乡地区Rh阴性无偿献血者Rh表型分布及RhD变异型基因型分析
分享到:

《新乡医学院学报》[ISSN:1004-7239/CN:41-1186/R]

卷:
40卷
期数:
2023年5
页码:
458-461
栏目:
临床研究
出版日期:
2023-05-05

文章信息/Info

Title:
Analysis of Rh phenotype distribution of Rh negative unpaid blood donors and RhD variant genotype in Xinxiang area
作者:
赵甜1张晨光2庞桂芝3
(1.新乡市中心医院检验科,河南 新乡 453000;2.新乡医学院公共卫生学院,河南 新乡 453003;3.新乡市中心血站血型室,河南 新乡 453001)
Author(s):
ZHAO Tian1ZHANG Chenguang2PANG Guizhi3
(1.Department of Clinical Laboratory,Xinxiang Central Hospital,Xinxiang 453000,Henan Province,China;2.School of Public Health,Xinxiang Medical University,Xinxiang 453003,Henan Province,China;3.Blood Group Room of Xinxiang Central Blood Station,Xinxiang 453001,Henan Province,China)
关键词:
D变异型RHD基因Sanger测序法输血治疗
Keywords:
D variantRHD geneSanger sequencingblood transfusion therapy
分类号:
R457.11
DOI:
10.7683/xxyxyxb.2023.05.011
文献标志码:
A
摘要:
目的 分析新乡地区Rh阴性无偿献血者Rh表型分布及RhD变异型基因型。
方法 选择2018年1月至2019年12月于新乡市中心血站无偿献血的110 667名无偿献血者为研究对象。采用试管法ABO正反定型试验检测ABO血型,采用试管法Rh抗原分型试验检测 Rh表型并初筛RhD阴性受试者,采用间接抗人球蛋白试验对初筛RhD阴性受试者进行RhD阴性确认,并检出 RhD变异型受试者。采用聚合酶链式反应法扩增RhD变异型受试者RHD基因外显子E1~E10,将扩增产物进行琼脂糖凝胶电泳,观察相应的外显子区域有无特异性条带出现。采用 Sanger测序法对RhD变异型受试者的RHD基因外显子E1~E10的特异性扩增产物进行基因测序,应用SeqMan软件分析基因序列,根据单核苷酸多态性位点确定RhD变异型。
结果 110 667名受试者中,初筛RhD阴性269例(0.24%)。269例初筛RhD阴性受试者中,Rh阴性256例(95.17%),RhD变异型 13例(4.83%)。256例RhD阴性受试者中,ABO血型为A型78例(30.47%)、B型92例(35.94%)、O型64例(25.00%)、AB型22例(8.59%),Rh表型分布以ccdee(60.55%)和Ccdee(29.30%)居多。11例RhD变异型受试者的RHD基因外显子E1~E10为特异性条带,2例RhD变异型受试者的RHD基因外显子E1~E5、E8、E10为特异性条带。13例RhD变异型受试者中,7例弱D型、4例DEL型和2例部分D型。13例RhD变异型受试者RHD基因RhCE表型分别为CCee(2/13)、Ccee(6/13)和ccEe(5/13)。7例RhD变异型受试者等位基因RHD\*15的E6外显子发生845G>A杂合突变。4例RhD变异型受试者的E9外显子发生1 227 G>A 杂合突变,其中1例受试者同时发生ZVS7+152 C>A突变。2例RhD变异型受试者的RHD基因E6~E9外显子发生突变,被RHCE基因所取代,表现为RHD-CE(6-9)-RHD。
结论 新乡地区RhD阴性无偿献血者中Rh表型分布以ccdee和Ccdee居多,RhD变异型以弱D型为主,其RHD等位基因为RHD\*15。
Abstract:
Objective To analyze the Rh phenotype distribution and RhD variant genotype of Rh negative unpaid blood donors in Xinxiang area.
Methods A total of 110 667 voluntary blood donors who donated blood at the Xinxiang Central Blood Station from January 2018 to December 2019 were selected as the research subjects.ABO blood type was detected by using the ABO positive and negative stereotyping test by tube method,Rh phenotype was detected by the in vitro Rh antigen typing test,and RhD negative subjects were initially screened.The RhD negative subjects in the initial screening were confirmed by indirect anti human globulin test,and RhD variant subjects were ultimately detected.The exons E1-E10 of RHD gene of RhD variant subjects were amplified by polymerase chain reaction,and the amplified products were subjected to agarose gel electrophoresis to observe whether there were specific bands in the corresponding exon regions.The specific amplification products of RHD gene exons E1-E10 in RhD variant subjects were sequenced by the Sanger sequencing method,the gene sequence was analyzed by SeqMan software,and the types of RhD variants was determined based on single nucleotide polymorphism loci.
Results Among 110 667 subjects,269 cases (0.24%) were negative for RhD during initial screening.Among the 269 initially screened RhD negative subjects,256 cases were RhD negative (95.17%) and 13 cases were RhD variant (4.83%).Among the 256 RhD negative subjects,there were 78 cases(30.47%) of type A,92 cases(35.94%) of type B,64 cases(25.00%) of type O,and 22 cases(8.59%) of type AB.The Rh phenotype distribution was mainly ccdee (60.55%) and Ccdee (29.30%).Eleven RhD variant subjects showed specific bands in exons E1-E10 of the RHD gene;two RhD variant subjects showed specific bands in exons E1-E5,E8,and E10 of the RHD gene.Among the 13 RhD variant subjects,7 cases were weak D type,4 cases were DEL type,and 2 cases were partial D type.The RhCE phenotypes of the RHD gene in 13 RhD variant subjects were CCee (2/13),Ccee (6/13),and ccEe (5/13),respectively.Seven RhD variant subjects experienced 845G>A heterozygous mutation in the E6 exon of the RHD \* 15 allele;four RhD variant subjects experienced 1 227 G>A heterozygous mutation in the E9 exon,with one subject experienced a IVS7+152 C>A mutation simultaneously;two RhD variant subjects had mutations in the E6-E9 exons of the RHD gene,which were replaced by the RHCE gene,exhibiting RHD-CE (6-9)-RHD.
Conclusion The Rh phenotype distribution of RhD negative unpaid blood donors in Xinxiang area is mainly ccdee and Ccdee,with the RhD variant mainly being weak D type,and the RHD allele is RHD\*15.

参考文献/References:

[1] SREELEKSHMI S,SHAMEE SHASTRY,POORNIMA BALIGA B.Variable reactivity of Rh D antigen and its serological characterization[J].Acta Clin Belg,2021,76(5):346-350.
[2] YANASIK M,OGUZ F S,BESISIK S K,et al.Frequency of RHD variants in serologically weak D Turkish blood donors[J].Transfus Apher Sci,2021,60(2):103024.
[3] 尚红,王毓三,申子瑜.全国临床检验操作规程(第4版)[M].北京:人民卫生出版社,2015:118-126.
SHANG H,WANG Y S,SHEN Z Y.National clinical laboratory operating procedures (4th edition) [M].Beijing:People′s Health Publishing House,2015:118-126.
[4] GAO M,CHEN Y P.The RHD variants in Chinese population[J].Blood Genom,2020,4(1):31-38.
[5] CHUNG Y N,KIM T Y,YU H,et al.Molecular basis of serological weak D phenotypes and RhD typing discrepancies identified in the Korean population[J].Blood Transfus,2021,19(4):327-334.
[6] 庞桂芝,臧文正,陈青,等.RhD变异型分子生物学特征及其临床意义[J].新乡医学院学报,2019,36(2):172-174.
PANG G Z,ZAGN W Z,CHEN Q,et al.Molecular biological charac-teristics of RhD variant and its clinical significance[J].J Xinxiang Med Univ,2019,36(2):172-174.
[7] SAFIC STANIC H,DOGIC V,HERCEG I,et al.D variants in the population of D-negative blood donors in the north-eastern region of Croatia[J].Transfus Med,2021,31(1):43-47.
[8] ZHANG X,LI G,ZHOU Z,et al.Molecular and computational analysis of 45 samples with a serologic weak D phenotype detected among 132 479 blood donors in northeast China[J].J Transl Med,2019,17(1):393.
[9] 张薇薇,左琴琴,毛娟,等.西安地区Rh阴性献血者抗原分布及D变异型分子机制的研究[J].中国输血杂志,2018,31(11):1223-1225.
ZHAGN W W,ZUO Q Q,MAO J,et al.Investigation of Rh phenotypes in RhD negative blood donors and the molecular mechanism of RhD variants in Xi′an blood donors[J].Chin J Blood Transfus,2018,31(11):1223-1225.
[10] 吴凡,梁爽,彭龙,等.38例血清学弱D表型献血者RhCcEe表型与RHD基因型检测情况分析[J].临床输血与检验,2021,23(5):632-639.
WU F,LIANG S,PENG L,et al.RhCE phenotyping and RHD genotyping for 38 blood donors with weak D phenotype[J].J Clin Transfus Labor Med,2021,23(5):632-639.
[11] 付绍杰,奉艳林,于立新,等.等候肾移植患者中RHD阴性血液样品的基因分型及意义[J].南方医科大学学报,2017,37(6):837-841.
FU S J,FENG Y L,YU L X,et al.Genotyping of RhD-negative blood samples diagnosed by serological tests from patients waiting for kidney transplantation[J].J Southern Med Univ,2017,37(6):837-841.
[12] WAH S T,CHI S N,KYAING K K,et al.Serological detection of Rh-Del phenotype among Rh-negative blood donors at national blood center,Yangon,Myanmar[J].Adv Hematol,2020,2020:3482124.
[13] 蒋玉林,毛伟,刘不尽,等.RhD阴性受血者输注DEL型血液诱发抗-D 1例[J].中国输血杂志,2021,34(3):308-311.
JIANG Y L,MAO W,LIU B J,et al.One case of RhD negative recipient receiving DEL type blood transfusion to induce anti D[J].Chin J Blood Transfus,2021,34(3):308-311.
[14] YIN" Q,FLEGEL W A.DEL in China:the D antigen among serologic RhD-negative individuals[J].J Transl Med,2021,19(1):439.
[15] ZONNEVELD R,KANHAI H H H,JAVADI A,et al.Frequency and characterization of RHD variants in serologically D-Surinamese pregnant women and D-newborns[J].Transfusion,2019,59(8):2672-2677.

相似文献/References:

[1]庞桂芝,臧文正,陈 青,等.RhD变异型分子生物学特征及其临床意义[J].新乡医学院学报,2019,36(2):172.[doi:10.7683/xxyxyxb.2019.02.018]
 PANG Gui-zhi,ZANG Wen-zheng,CHEN Qing,et al.Molecular biological characteristics of RhD variant and its clinical significance[J].Journal of Xinxiang Medical University,2019,36(5):172.[doi:10.7683/xxyxyxb.2019.02.018]

更新日期/Last Update: 2023-05-05