在免疫监测下评估儿童肝移植免疫抑制的充分性：我们做到了吗？

IF 2.2 4区医学 Q3 IMMUNOLOGY

Human Immunology Pub Date : 2025-09-01 DOI:10.1016/j.humimm.2025.111580

Anushka Das , Mia Feller , Jaeil Ahn , Nada Yazigi , Khalid Khan , Alexander Kroemer , Thomas Fishbein , Olga Timofeeva , Udeme D. Ekong

{"title":"在免疫监测下评估儿童肝移植免疫抑制的充分性：我们做到了吗？","authors":"Anushka Das , Mia Feller , Jaeil Ahn , Nada Yazigi , Khalid Khan , Alexander Kroemer , Thomas Fishbein , Olga Timofeeva , Udeme D. Ekong","doi":"10.1016/j.humimm.2025.111580","DOIUrl":null,"url":null,"abstract":"<div><div>Current approaches used for pediatric liver transplant (LT) surveillance have diagnostic limitations. We used pleximmune™ immune reactivity index (IRI) and anti-HLA donor specific antibody (DSA) to predict the adequacy of immunosuppression (IS) relative to risk of acute cellular rejection (ACR) at 1-year post LT. This is a retrospective chart review of children who underwent LT between January 1, 2016, through December 31, 2020, and had at least one pleximmune<sup>TM</sup> measurement performed within 60-days of a liver biopsy. There were 45 liver biopsies with accompanying pleximmune<sup>TM</sup> in 31 children. An inverse correlation was observed between tacrolimus level and IRI (R = -0.34; p = 0.039). The sensitivity, specificity, positive and negative predictive values of IRI for diagnosis of ACR was 55 %, 65 %, 33 % and 81 % respectively. The combination of DSA and IRI had a specificity of 92 % and negative predictive value of 89 % for ACR. In conclusion, a high IRI identifies recipients with low tacrolimus levels. Thus, the associations observed in this non-standardized cohort support the use of pleximmune<sup>TM</sup> IRI in combination with DSA, for hypothesis generation in future studies involving post liver transplant graft immune surveillance.</div></div>","PeriodicalId":55047,"journal":{"name":"Human Immunology","volume":"86 5","pages":"Article 111580"},"PeriodicalIF":2.2000,"publicationDate":"2025-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Assessing the adequacy of immunosuppression in pediatric liver transplantation with immune Monitoring: Are we there yet?\",\"authors\":\"Anushka Das , Mia Feller , Jaeil Ahn , Nada Yazigi , Khalid Khan , Alexander Kroemer , Thomas Fishbein , Olga Timofeeva , Udeme D. Ekong\",\"doi\":\"10.1016/j.humimm.2025.111580\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Current approaches used for pediatric liver transplant (LT) surveillance have diagnostic limitations. We used pleximmune™ immune reactivity index (IRI) and anti-HLA donor specific antibody (DSA) to predict the adequacy of immunosuppression (IS) relative to risk of acute cellular rejection (ACR) at 1-year post LT. This is a retrospective chart review of children who underwent LT between January 1, 2016, through December 31, 2020, and had at least one pleximmune<sup>TM</sup> measurement performed within 60-days of a liver biopsy. There were 45 liver biopsies with accompanying pleximmune<sup>TM</sup> in 31 children. An inverse correlation was observed between tacrolimus level and IRI (R = -0.34; p = 0.039). The sensitivity, specificity, positive and negative predictive values of IRI for diagnosis of ACR was 55 %, 65 %, 33 % and 81 % respectively. The combination of DSA and IRI had a specificity of 92 % and negative predictive value of 89 % for ACR. In conclusion, a high IRI identifies recipients with low tacrolimus levels. Thus, the associations observed in this non-standardized cohort support the use of pleximmune<sup>TM</sup> IRI in combination with DSA, for hypothesis generation in future studies involving post liver transplant graft immune surveillance.</div></div>\",\"PeriodicalId\":55047,\"journal\":{\"name\":\"Human Immunology\",\"volume\":\"86 5\",\"pages\":\"Article 111580\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2025-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Human Immunology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0198885925003519\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"IMMUNOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Human Immunology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0198885925003519","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"IMMUNOLOGY","Score":null,"Total":0}

引用次数: 0

摘要

目前用于儿童肝移植（LT）监测的方法具有诊断局限性。我们使用pleximmune™免疫反应指数（IRI）和抗hla供体特异性抗体（DSA）来预测LT后1年免疫抑制（IS）相对于急性细胞排斥（ACR）风险的适当性。这是一项回顾性图表回顾，研究对象是2016年1月1日至2020年12月31日期间接受LT治疗的儿童，并且在肝活检后60天内进行了至少一次pleximmuneTM测量。在31例患儿中，有45例肝活检伴丛免疫etm。他克莫司水平与IRI呈负相关（R = -0.34; p = 0.039）。IRI诊断ACR的敏感性为55%，特异性为65%，阳性预测值为33%，阴性预测值为81%。DSA联合IRI对ACR的特异性为92%，阴性预测值为89%。总之，高IRI可识别低他克莫司水平的受体。因此，在这个非标准化队列中观察到的关联支持将pleximmuneTM IRI联合DSA用于未来涉及肝移植后移植物免疫监测的研究中。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

查看原文本刊更多论文

Assessing the adequacy of immunosuppression in pediatric liver transplantation with immune Monitoring: Are we there yet?

Current approaches used for pediatric liver transplant (LT) surveillance have diagnostic limitations. We used pleximmune™ immune reactivity index (IRI) and anti-HLA donor specific antibody (DSA) to predict the adequacy of immunosuppression (IS) relative to risk of acute cellular rejection (ACR) at 1-year post LT. This is a retrospective chart review of children who underwent LT between January 1, 2016, through December 31, 2020, and had at least one pleximmune^TM measurement performed within 60-days of a liver biopsy. There were 45 liver biopsies with accompanying pleximmune^TM in 31 children. An inverse correlation was observed between tacrolimus level and IRI (R = -0.34; p = 0.039). The sensitivity, specificity, positive and negative predictive values of IRI for diagnosis of ACR was 55 %, 65 %, 33 % and 81 % respectively. The combination of DSA and IRI had a specificity of 92 % and negative predictive value of 89 % for ACR. In conclusion, a high IRI identifies recipients with low tacrolimus levels. Thus, the associations observed in this non-standardized cohort support the use of pleximmune^TM IRI in combination with DSA, for hypothesis generation in future studies involving post liver transplant graft immune surveillance.

求助全文

通过发布文献求助，成功后即可免费获取论文全文。去求助

来源期刊

Human Immunology 医学-免疫学

CiteScore

5.40

自引率

7.40%

发文量

107

审稿时长

12 days

期刊介绍： The journal''s scope includes understanding the genetic and functional mechanisms that distinguish human individuals in their immune responses to allografts, pregnancy, infections or vaccines as well as the immune responses that lead to autoimmunity, allergy or drug hypersensitivity. It also includes examining the distribution of the genes controlling these responses in populations. Research areas include: Studies of the genetics, genomics, polymorphism, evolution, and population distribution of immune-related genes Studies of the expression, structure and function of the products of immune-related genes Immunogenetics of susceptibility to infectious and autoimmune disease, and allergy The role of the immune-related genes in hematopoietic stem cell, solid organ, and vascularized composite allograft transplant Histocompatibility studies including alloantibodies, epitope definition, and T cell alloreactivity Studies of immunologic tolerance and pregnancy T cell, B cell, NK and regulatory cell functions, particularly related to subjects within the journal''s scope Pharmacogenomics and vaccine development in the context of immune-related genes Human Immunology considers immune-related genes to include those encoding classical and non-classical HLA, KIR, MIC, minor histocompatibility antigens (mHAg), immunoglobulins, TCR, BCR, proteins involved in antigen processing and presentation, complement, Fc receptors, chemokines and cytokines. Other immune-related genes may be considered. Human Immunology is also interested in bioinformatics of immune-related genes and organizational topics impacting laboratory processes, organ allocation, clinical strategies, and registries related to autoimmunity and transplantation.