R. F. Kermond, S. Kim, F. Mackie, D. Hahn, R. P. Carroll, A. Sharma, A. M. Durkan
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Of 71 individuals, 72% recorded a positive pre-transplant AT1R Ab level (≥17 U/mL). Over a median follow-up of 4.7 years, AT1R Ab positivity demonstrated a trend towards increased risk of rejection however was not statistically significant (HR 3.45, 95% CI 0.97–12.35, <i>p</i>-value 0.06). Sensitivity analysis with AT1R Ab levels of ≥25 U/mL (HR 2.05 95% CI 0.78–5.39, <i>p</i>-value 0.14) and ≥40 U/mL (HR 1.32, CI 95% 0.55–3.17, <i>p</i>-value 0.53) validated this. De novo DSA formation occurred more frequently with AT1R Ab positivity (41% vs. 20%, <i>p</i>-value 0.9). AT1R Ab was not associated with hypertension, proteinuria, graft failure or dysfunction. In conclusion, this cohort study demonstrated a high prevalence of pre-transplant AT1R Ab positivity (72%). AT1R Ab positivity demonstrated a trend towards increased risk of rejection and de novo DSA formation however did not meet statistical significance. There was no association between AT1R Ab and hypertension, proteinuria, graft failure or dysfunction.</p>","PeriodicalId":13172,"journal":{"name":"HLA","volume":"104 3","pages":""},"PeriodicalIF":5.9000,"publicationDate":"2024-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/tan.15649","citationCount":"0","resultStr":"{\"title\":\"Effect of angiotensin II type 1 receptor antibodies on graft function and survival in paediatric kidney transplant recipients\",\"authors\":\"R. F. Kermond, S. Kim, F. Mackie, D. Hahn, R. P. Carroll, A. Sharma, A. M. Durkan\",\"doi\":\"10.1111/tan.15649\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>HLA donor specific antibodies (DSA) are implicated in antibody-mediated rejection (AMR), graft dysfunction and failure in kidney transplant (KT) recipients. Non-HLA antibodies including angiotensin II type 1 receptor (AT1R) may also play a role in AMR, impact graft function and survival. Data is limited in paediatric KT cohorts. We aimed to assess the prevalence and effect of pre-transplant AT1R antibodies on rejection, graft function and survival in paediatric KT recipients. This was a retrospective cohort study conducted across two paediatric centres including KT recipients with a pre-transplant AT1R antibody level. Outcomes included rejection, de novo DSA formation, graft function, failure, proteinuria and hypertension. Of 71 individuals, 72% recorded a positive pre-transplant AT1R Ab level (≥17 U/mL). Over a median follow-up of 4.7 years, AT1R Ab positivity demonstrated a trend towards increased risk of rejection however was not statistically significant (HR 3.45, 95% CI 0.97–12.35, <i>p</i>-value 0.06). Sensitivity analysis with AT1R Ab levels of ≥25 U/mL (HR 2.05 95% CI 0.78–5.39, <i>p</i>-value 0.14) and ≥40 U/mL (HR 1.32, CI 95% 0.55–3.17, <i>p</i>-value 0.53) validated this. De novo DSA formation occurred more frequently with AT1R Ab positivity (41% vs. 20%, <i>p</i>-value 0.9). AT1R Ab was not associated with hypertension, proteinuria, graft failure or dysfunction. In conclusion, this cohort study demonstrated a high prevalence of pre-transplant AT1R Ab positivity (72%). AT1R Ab positivity demonstrated a trend towards increased risk of rejection and de novo DSA formation however did not meet statistical significance. 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引用次数: 0
摘要
HLA供体特异性抗体(DSA)与抗体介导的排斥反应(AMR)、肾移植(KT)受者的移植物功能障碍和失败有关。包括血管紧张素 II 1 型受体(AT1R)在内的非 HLA 抗体也可能在 AMR 中发挥作用,影响移植物功能和存活率。儿科 KT 队列中的数据有限。我们旨在评估移植前AT1R抗体的发生率及其对儿科KT受者排斥反应、移植物功能和存活率的影响。这是一项在两个儿科中心进行的回顾性队列研究,包括移植前存在 AT1R 抗体水平的 KT 受者。研究结果包括排斥反应、新DSA形成、移植功能、失败、蛋白尿和高血压。在 71 例受者中,72% 的受者移植前 AT1R 抗体水平呈阳性(≥17 U/mL)。在中位 4.7 年的随访中,AT1R Ab 阳性显示出排斥风险增加的趋势,但无统计学意义(HR 3.45,95% CI 0.97-12.35,P 值 0.06)。AT1R Ab 水平≥25 U/mL(HR 2.05 95% CI 0.78-5.39,P 值 0.14)和≥40 U/mL(HR 1.32,CI 95% 0.55-3.17,P 值 0.53)的敏感性分析证实了这一点。AT1R抗体阳性者更易形成新的DSA(41%对20%,P值0.9)。AT1R Ab 与高血压、蛋白尿、移植失败或功能障碍无关。总之,这项队列研究显示,移植前AT1R抗体阳性率很高(72%)。AT1R抗体阳性有增加排斥反应和新发DSA形成风险的趋势,但未达到统计学意义。AT1R Ab 与高血压、蛋白尿、移植失败或功能障碍之间没有关联。
Effect of angiotensin II type 1 receptor antibodies on graft function and survival in paediatric kidney transplant recipients
HLA donor specific antibodies (DSA) are implicated in antibody-mediated rejection (AMR), graft dysfunction and failure in kidney transplant (KT) recipients. Non-HLA antibodies including angiotensin II type 1 receptor (AT1R) may also play a role in AMR, impact graft function and survival. Data is limited in paediatric KT cohorts. We aimed to assess the prevalence and effect of pre-transplant AT1R antibodies on rejection, graft function and survival in paediatric KT recipients. This was a retrospective cohort study conducted across two paediatric centres including KT recipients with a pre-transplant AT1R antibody level. Outcomes included rejection, de novo DSA formation, graft function, failure, proteinuria and hypertension. Of 71 individuals, 72% recorded a positive pre-transplant AT1R Ab level (≥17 U/mL). Over a median follow-up of 4.7 years, AT1R Ab positivity demonstrated a trend towards increased risk of rejection however was not statistically significant (HR 3.45, 95% CI 0.97–12.35, p-value 0.06). Sensitivity analysis with AT1R Ab levels of ≥25 U/mL (HR 2.05 95% CI 0.78–5.39, p-value 0.14) and ≥40 U/mL (HR 1.32, CI 95% 0.55–3.17, p-value 0.53) validated this. De novo DSA formation occurred more frequently with AT1R Ab positivity (41% vs. 20%, p-value 0.9). AT1R Ab was not associated with hypertension, proteinuria, graft failure or dysfunction. In conclusion, this cohort study demonstrated a high prevalence of pre-transplant AT1R Ab positivity (72%). AT1R Ab positivity demonstrated a trend towards increased risk of rejection and de novo DSA formation however did not meet statistical significance. There was no association between AT1R Ab and hypertension, proteinuria, graft failure or dysfunction.
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.