Anne M Halpin,Cathi Murphey,Bruce Motyka,Caishun Li,Jean Pearcey,Maria Ellis,I Esme Dijke,Simon Urschel,Adam Bingaman,Tess Van Ong,Matthias Kapturczak,Todd L Lowary,Christopher W Cairo,Lori J West
{"title":"abo - a2不相容肾移植的多重头免疫分析。","authors":"Anne M Halpin,Cathi Murphey,Bruce Motyka,Caishun Li,Jean Pearcey,Maria Ellis,I Esme Dijke,Simon Urschel,Adam Bingaman,Tess Van Ong,Matthias Kapturczak,Todd L Lowary,Christopher W Cairo,Lori J West","doi":"10.1016/j.ajt.2025.04.003","DOIUrl":null,"url":null,"abstract":"Kidney transplantation from ABO-A2 donors into ABO-O and -B recipients can alleviate inequitable transplant access created by ABO demographics. ABO-A2-incompatible eligibility is determined by anti-A hemagglutination titres. However, titres do not distinguish antibodies specific for A-II glycans, the sole A-antigen subtype in vascular endothelium, from other anti-A antibodies. We examined whether reliance on anti-A titres unnecessarily limited ABO-A2-incompatible transplants for candidates with low anti-A-II levels. We created a single-antigen-bead immunoassay for ABO antibodies, confirmed the specificity and reproducibility, and demonstrated the ability to detect anti-A and -B glycan-subtype-specific antibodies in healthy control sera. We then measured subtype-specific anti-A antibodies in original sera from ABO-B and -O candidates who had been previously evaluated for ABO-A2-incompatible eligibility. Anti-A-II levels in candidates who had been deemed ineligible (anti-A titres >4) were compared to eligible candidates (anti-A titres ≤4) who had subsequently received ABO-A2-incompatible kidneys. Of 141 candidates, 75(53%) were ineligible; 66(47%) were eligible and received ABO-A2 kidneys. Re-testing original sera, 55%(41/75) of ineligible candidates had anti-A-II levels comparable to eligible candidates. Anti-A titres did not reflect anti-A-II levels. Our ABO antibody assay reproducibly measures graft-specific anti-A-II antibodies, providing information beyond anti-A titres that may increase transplant access for ABO-B and -O candidates.","PeriodicalId":123,"journal":{"name":"American Journal of Transplantation","volume":"50 1","pages":""},"PeriodicalIF":8.9000,"publicationDate":"2025-04-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Multiplex bead immunoassay in ABO-A2-incompatible kidney transplantation.\",\"authors\":\"Anne M Halpin,Cathi Murphey,Bruce Motyka,Caishun Li,Jean Pearcey,Maria Ellis,I Esme Dijke,Simon Urschel,Adam Bingaman,Tess Van Ong,Matthias Kapturczak,Todd L Lowary,Christopher W Cairo,Lori J West\",\"doi\":\"10.1016/j.ajt.2025.04.003\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Kidney transplantation from ABO-A2 donors into ABO-O and -B recipients can alleviate inequitable transplant access created by ABO demographics. ABO-A2-incompatible eligibility is determined by anti-A hemagglutination titres. However, titres do not distinguish antibodies specific for A-II glycans, the sole A-antigen subtype in vascular endothelium, from other anti-A antibodies. We examined whether reliance on anti-A titres unnecessarily limited ABO-A2-incompatible transplants for candidates with low anti-A-II levels. We created a single-antigen-bead immunoassay for ABO antibodies, confirmed the specificity and reproducibility, and demonstrated the ability to detect anti-A and -B glycan-subtype-specific antibodies in healthy control sera. We then measured subtype-specific anti-A antibodies in original sera from ABO-B and -O candidates who had been previously evaluated for ABO-A2-incompatible eligibility. Anti-A-II levels in candidates who had been deemed ineligible (anti-A titres >4) were compared to eligible candidates (anti-A titres ≤4) who had subsequently received ABO-A2-incompatible kidneys. Of 141 candidates, 75(53%) were ineligible; 66(47%) were eligible and received ABO-A2 kidneys. Re-testing original sera, 55%(41/75) of ineligible candidates had anti-A-II levels comparable to eligible candidates. Anti-A titres did not reflect anti-A-II levels. Our ABO antibody assay reproducibly measures graft-specific anti-A-II antibodies, providing information beyond anti-A titres that may increase transplant access for ABO-B and -O candidates.\",\"PeriodicalId\":123,\"journal\":{\"name\":\"American Journal of Transplantation\",\"volume\":\"50 1\",\"pages\":\"\"},\"PeriodicalIF\":8.9000,\"publicationDate\":\"2025-04-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"American Journal of Transplantation\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1016/j.ajt.2025.04.003\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"SURGERY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Journal of Transplantation","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.ajt.2025.04.003","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"SURGERY","Score":null,"Total":0}
Multiplex bead immunoassay in ABO-A2-incompatible kidney transplantation.
Kidney transplantation from ABO-A2 donors into ABO-O and -B recipients can alleviate inequitable transplant access created by ABO demographics. ABO-A2-incompatible eligibility is determined by anti-A hemagglutination titres. However, titres do not distinguish antibodies specific for A-II glycans, the sole A-antigen subtype in vascular endothelium, from other anti-A antibodies. We examined whether reliance on anti-A titres unnecessarily limited ABO-A2-incompatible transplants for candidates with low anti-A-II levels. We created a single-antigen-bead immunoassay for ABO antibodies, confirmed the specificity and reproducibility, and demonstrated the ability to detect anti-A and -B glycan-subtype-specific antibodies in healthy control sera. We then measured subtype-specific anti-A antibodies in original sera from ABO-B and -O candidates who had been previously evaluated for ABO-A2-incompatible eligibility. Anti-A-II levels in candidates who had been deemed ineligible (anti-A titres >4) were compared to eligible candidates (anti-A titres ≤4) who had subsequently received ABO-A2-incompatible kidneys. Of 141 candidates, 75(53%) were ineligible; 66(47%) were eligible and received ABO-A2 kidneys. Re-testing original sera, 55%(41/75) of ineligible candidates had anti-A-II levels comparable to eligible candidates. Anti-A titres did not reflect anti-A-II levels. Our ABO antibody assay reproducibly measures graft-specific anti-A-II antibodies, providing information beyond anti-A titres that may increase transplant access for ABO-B and -O candidates.
期刊介绍:
The American Journal of Transplantation is a leading journal in the field of transplantation. It serves as a forum for debate and reassessment, an agent of change, and a major platform for promoting understanding, improving results, and advancing science. Published monthly, it provides an essential resource for researchers and clinicians worldwide.
The journal publishes original articles, case reports, invited reviews, letters to the editor, critical reviews, news features, consensus documents, and guidelines over 12 issues a year. It covers all major subject areas in transplantation, including thoracic (heart, lung), abdominal (kidney, liver, pancreas, islets), tissue and stem cell transplantation, organ and tissue donation and preservation, tissue injury, repair, inflammation, and aging, histocompatibility, drugs and pharmacology, graft survival, and prevention of graft dysfunction and failure. It also explores ethical and social issues in the field.