Schmidt Franziska, Verboom Murielle, Hallensleben Michael, Braumann Alexander, Drube Jens, Brunkhorst Lena, Haffner Dieter, Melk Anette, Kanzelmeyer Nele
Department of Pediatric Kidney, Liver, Metabolic and Neurological Diseases, Hannover Medical School, Hannover, Germany.
Institute of Transfusion Medicine and Transplant Engineering, Hannover Medical School, Hannover, Germany.
Transpl Int. 2025 Aug 7;38:14463. doi: 10.3389/ti.2025.14463. eCollection 2025.
Antibody-mediated rejection (ABMR) is the leading cause of long-term graft loss in pediatric kidney transplantation (KTx). While donor-specific HLA antibodies are established contributors, emerging evidence suggests a role for non-HLA antibodies in ABMR pathogenesis. In this descriptive study, we analyzed 60 non-HLA antibodies in 77 pediatric KTx recipients using serum samples collected pre-transplant, post-transplant, and at ABMR diagnosis. During a median follow-up of 4.83 years, 29.8% developed ABMR, with a median onset of 3.67 years. Non-HLA antibody presence prior to KTx was not influenced by pre-transplant dialysis; over half of the patients already had >15 positive non-HLA antibodies. The cumulative antibody profile remained stable 1-2 years post-KTx, with no association between late ABMR and antibody strength or breadth. However, ACTIN (higher risk) and CGB5 (lower risk) at 1-2 years post-KTx, as well as SNRPB2 pre-transplant, were significantly associated with ABMR (p < 0.05). IL-21 levels increased in controls over time (p < 0.05), although driven by five patients with notably high levels. Our findings support a potential involvement of non-HLA antibodies in pediatric ABMR. Nevertheless, larger studies are needed to validate the predictive value of individual non-HLA antibodies for clinical application.
抗体介导的排斥反应(ABMR)是小儿肾移植(KTx)中长期移植肾丢失的主要原因。虽然供者特异性HLA抗体是公认的促成因素,但新出现的证据表明非HLA抗体在ABMR发病机制中也起作用。在这项描述性研究中,我们使用移植前、移植后及ABMR诊断时采集的血清样本,分析了77例小儿KTx受者体内的60种非HLA抗体。在中位随访4.83年期间,29.8%的患者发生了ABMR,中位发病时间为3.67年。KTx前非HLA抗体的存在不受移植前透析的影响;超过半数的患者已有超过15种阳性非HLA抗体。移植后1 - 2年累积抗体谱保持稳定,晚期ABMR与抗体强度或广度之间无关联。然而,移植后1 - 2年的肌动蛋白(ACTIN,高风险)和绒毛膜促性腺激素β亚基(CGB5,低风险),以及移植前 的小核核糖核蛋白多肽B2(SNRPB2)与ABMR显著相关(p < 0.05)。对照组中白细胞介素-21(IL-21)水平随时间升高(p < 0.05),尽管是由5例水平显著升高的患者驱动的。我们的研究结果支持非HLA抗体可能参与小儿ABMR。然而,需要更大规模的研究来验证单个非HLA抗体在临床应用中的预测价值。