Xiao-Yan Li, Qiong-Fei Deng, Xiao-Li Lai, Dan-Dan Chen, Dan Wang, Xuan Zeng
{"title":"[j (a-b-)家族的分子生物学机制和输血策略]。","authors":"Xiao-Yan Li, Qiong-Fei Deng, Xiao-Li Lai, Dan-Dan Chen, Dan Wang, Xuan Zeng","doi":"10.19746/j.cnki.issn.1009-2137.2025.03.037","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>To investigate the molecular mechanism and explore blood transfusion strategies for a proband exhibiting the JK (a-b-) phenotype and anti-JK<sup>3</sup> high frequency antigen antibody and her eight family members.</p><p><strong>Methods: </strong>The Kidd blood phenotype and irregular antibodies in a family were identified by serologic tests. Exon 4-11 and intron region of <i>SLC14A1</i> gene were sequenced by Sanger method.</p><p><strong>Results: </strong>The combination of the gene <i>JK*B</i> (c.499A>G,c.512G>A,c.588A>G) and gene <i>JK*B</i> (c.342-1G>A,588A>G) in this family were considered to result in the JK (a-b-) phenotype in two members. The members carrying gene <i>JK*A</i>(c.130G>A,588A>G) all present serological JK<sup>a+W</sup>. Members carrying gene <i>JK*B</i> (c.499A>G,c.588A>G) all present serological JK<sup>b+W</sup>, which has not been previously reported to cause antigenic weakening. The proband with JK (a-b-) phenotype produced anti-JK<sup>3</sup> antibodies, the hospital formulated a number of blood preparation strategies for the patient and she was discharged after recovery.</p><p><strong>Conclusion: </strong>In this study, the molecular mechanism of JK (a-b-) in this family was identified, the transfusion strategy of rare blood group was established in our institution preliminary, and the necessity of establishing a rare blood group bank was revealed in this region. It is suggested that <i>JK*B</i> (c.499A>G,c.588A>G) may be a new genetic pattern leading to the weakening of Kidd antigenicity, which lays a foundation for the study of population genetics.</p>","PeriodicalId":35777,"journal":{"name":"中国实验血液学杂志","volume":"33 3","pages":"869-874"},"PeriodicalIF":0.0000,"publicationDate":"2025-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[Molecular Biological Mechanism and Transfusion Strategy of a Jk(a-b-) Family].\",\"authors\":\"Xiao-Yan Li, Qiong-Fei Deng, Xiao-Li Lai, Dan-Dan Chen, Dan Wang, Xuan Zeng\",\"doi\":\"10.19746/j.cnki.issn.1009-2137.2025.03.037\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>To investigate the molecular mechanism and explore blood transfusion strategies for a proband exhibiting the JK (a-b-) phenotype and anti-JK<sup>3</sup> high frequency antigen antibody and her eight family members.</p><p><strong>Methods: </strong>The Kidd blood phenotype and irregular antibodies in a family were identified by serologic tests. Exon 4-11 and intron region of <i>SLC14A1</i> gene were sequenced by Sanger method.</p><p><strong>Results: </strong>The combination of the gene <i>JK*B</i> (c.499A>G,c.512G>A,c.588A>G) and gene <i>JK*B</i> (c.342-1G>A,588A>G) in this family were considered to result in the JK (a-b-) phenotype in two members. The members carrying gene <i>JK*A</i>(c.130G>A,588A>G) all present serological JK<sup>a+W</sup>. Members carrying gene <i>JK*B</i> (c.499A>G,c.588A>G) all present serological JK<sup>b+W</sup>, which has not been previously reported to cause antigenic weakening. The proband with JK (a-b-) phenotype produced anti-JK<sup>3</sup> antibodies, the hospital formulated a number of blood preparation strategies for the patient and she was discharged after recovery.</p><p><strong>Conclusion: </strong>In this study, the molecular mechanism of JK (a-b-) in this family was identified, the transfusion strategy of rare blood group was established in our institution preliminary, and the necessity of establishing a rare blood group bank was revealed in this region. It is suggested that <i>JK*B</i> (c.499A>G,c.588A>G) may be a new genetic pattern leading to the weakening of Kidd antigenicity, which lays a foundation for the study of population genetics.</p>\",\"PeriodicalId\":35777,\"journal\":{\"name\":\"中国实验血液学杂志\",\"volume\":\"33 3\",\"pages\":\"869-874\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"中国实验血液学杂志\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.19746/j.cnki.issn.1009-2137.2025.03.037\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"中国实验血液学杂志","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.19746/j.cnki.issn.1009-2137.2025.03.037","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
[Molecular Biological Mechanism and Transfusion Strategy of a Jk(a-b-) Family].
Objective: To investigate the molecular mechanism and explore blood transfusion strategies for a proband exhibiting the JK (a-b-) phenotype and anti-JK3 high frequency antigen antibody and her eight family members.
Methods: The Kidd blood phenotype and irregular antibodies in a family were identified by serologic tests. Exon 4-11 and intron region of SLC14A1 gene were sequenced by Sanger method.
Results: The combination of the gene JK*B (c.499A>G,c.512G>A,c.588A>G) and gene JK*B (c.342-1G>A,588A>G) in this family were considered to result in the JK (a-b-) phenotype in two members. The members carrying gene JK*A(c.130G>A,588A>G) all present serological JKa+W. Members carrying gene JK*B (c.499A>G,c.588A>G) all present serological JKb+W, which has not been previously reported to cause antigenic weakening. The proband with JK (a-b-) phenotype produced anti-JK3 antibodies, the hospital formulated a number of blood preparation strategies for the patient and she was discharged after recovery.
Conclusion: In this study, the molecular mechanism of JK (a-b-) in this family was identified, the transfusion strategy of rare blood group was established in our institution preliminary, and the necessity of establishing a rare blood group bank was revealed in this region. It is suggested that JK*B (c.499A>G,c.588A>G) may be a new genetic pattern leading to the weakening of Kidd antigenicity, which lays a foundation for the study of population genetics.