A Cautionary Tale: ABO Genotyping in Kidney Transplantation of ABO A2 Kidneys Into B or O Recipients

IF 5.9 4区 医学 Q2 CELL BIOLOGY
HLA Pub Date : 2025-02-11 DOI:10.1111/tan.70081
Cathi L. Murphey, Amanda Bailey, Matthias Kapturczak, Howard M. Gebel, Robert A. Bray
{"title":"A Cautionary Tale: ABO Genotyping in Kidney Transplantation of ABO A2 Kidneys Into B or O Recipients","authors":"Cathi L. Murphey,&nbsp;Amanda Bailey,&nbsp;Matthias Kapturczak,&nbsp;Howard M. Gebel,&nbsp;Robert A. Bray","doi":"10.1111/tan.70081","DOIUrl":null,"url":null,"abstract":"<div>\n \n <p>The US 2014 kidney allocation system (KAS) allows ABO A<sub>2</sub> donor kidneys to be transplanted into ABO B candidates, thereby broadening the donor pool for a traditionally disadvantaged population. Safely transplanting these patients relies heavily on two components: (1) recipient ABO antibody titres and (2) ABO A subtyping of the donor. While lectin-based serological methods remain the gold standard for ABO typing, recent data show ABO molecular genotyping is a more reliable approach to accurately assign the A<sub>2</sub> subtype. ABO titres were performed using Ortho Diagnostics gel cards using haemagglutination by both antiglobulin-enhanced and dithiothreitol methods. ABO genotyping was performed using innotrain diagnostiks Real-Time PCR. Here, we present two cases where ABO lectin testing incorrectly identified the donors as ABO A<sub>2</sub> and A<sub>2</sub>B instead of A<sub>1</sub> and A<sub>1</sub>B. Consequently, the transplants proceeded but had deleterious outcomes. These two cases support the concept that ABO genotyping by molecular methodology should be mandatory to confirm the A<sub>2</sub> donor subtype when transplanting kidneys from deceased donors into ABO B candidates on the waitlist and for virtual crossmatching (VXM) donors being considered for transplantation into ABO B and O recipients.</p>\n </div>","PeriodicalId":13172,"journal":{"name":"HLA","volume":"105 2","pages":""},"PeriodicalIF":5.9000,"publicationDate":"2025-02-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"HLA","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/tan.70081","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

The US 2014 kidney allocation system (KAS) allows ABO A2 donor kidneys to be transplanted into ABO B candidates, thereby broadening the donor pool for a traditionally disadvantaged population. Safely transplanting these patients relies heavily on two components: (1) recipient ABO antibody titres and (2) ABO A subtyping of the donor. While lectin-based serological methods remain the gold standard for ABO typing, recent data show ABO molecular genotyping is a more reliable approach to accurately assign the A2 subtype. ABO titres were performed using Ortho Diagnostics gel cards using haemagglutination by both antiglobulin-enhanced and dithiothreitol methods. ABO genotyping was performed using innotrain diagnostiks Real-Time PCR. Here, we present two cases where ABO lectin testing incorrectly identified the donors as ABO A2 and A2B instead of A1 and A1B. Consequently, the transplants proceeded but had deleterious outcomes. These two cases support the concept that ABO genotyping by molecular methodology should be mandatory to confirm the A2 donor subtype when transplanting kidneys from deceased donors into ABO B candidates on the waitlist and for virtual crossmatching (VXM) donors being considered for transplantation into ABO B and O recipients.

求助全文
约1分钟内获得全文 求助全文
来源期刊
HLA
HLA Immunology and Microbiology-Immunology
CiteScore
3.00
自引率
28.80%
发文量
368
期刊介绍: HLA, the journal, publishes articles on various aspects of immunogenetics. These include the immunogenetics of cell surface antigens, the ontogeny and phylogeny of the immune system, the immunogenetics of cell interactions, the functional aspects of cell surface molecules and their natural ligands, and the role of tissue antigens in immune reactions. Additionally, the journal covers experimental and clinical transplantation, the relationships between normal tissue antigens and tumor-associated antigens, the genetic control of immune response and disease susceptibility, and the biochemistry and molecular biology of alloantigens and leukocyte differentiation. Manuscripts on molecules expressed on lymphoid cells, myeloid cells, platelets, and non-lineage-restricted antigens are welcomed. Lastly, the journal focuses on the immunogenetics of histocompatibility antigens in both humans and experimental animals, including their tissue distribution, regulation, and expression in normal and malignant cells, as well as the use of antigens as markers for disease.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信