Philippe Aurélie, Arns Wolfgang, Ditt Vanessa, Hauser Ingeborg A, Thaiss Friedrich, Sommerer Claudia, Suwelack Barbara, Dragun Duska, Hillen Jan, Schiedel Christiane, Elsässer Anja, Nashan Björn
BIH Biomedical Innovation Academy, Berlin Institute of Health at Charité-Universitätsmedizin Berlin, Berlin, Germany.
Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Clinic for Nephrology and Critical Care Medicine, Campus Virchow-Klinikum, Berlin, Germany.
Front Transplant. 2023 Nov 21;2:1273890. doi: 10.3389/frtra.2023.1273890. eCollection 2023.
Non-human leukocyte antigen (non-HLA) antibodies including antibodies targeting Angiotensin II type 1 (AT1R) and Endothelin-1 type A (ETAR) receptors represent a topic of interest in kidney transplantation (KTx). This exploratory substudy evaluated the impact of everolimus (EVR) or mycophenolic acid (MPA) in combination with tacrolimus (TAC) or cyclosporine A (CsA) in patients with preformed non-HLA antibodies, potentially associated rejections and/or their impact on renal function over 1 year.
All eligible patients were randomized (1:1:1) before transplantation to receive either EVR/TAC, EVR/CsA, or MPA/TAC regimen. The effect of these regimens on the formation of non-HLA antibodies within one year post KTx and the association with clinical events was evaluated descriptively in randomized ( = 268) population.
At Month 12, in EVR/TAC group, higher incidence of patients negative for AT1R- and ETAR-antibodies (82.2% and 76.7%, respectively) was noted, whereas the incidence of AT1R- and ETAR-antibodies positivity (28.1% and 34.7%, respectively) was higher in the MPA/TAC group. Non-HLA antibodies had no influence on clinical outcomes in any treatment group and no graft loss or death was reported.
The studied combinations of immunosuppressants were safe with no influence on clinical outcomes and suggested minimal exposure of calcineurin inhibitors for better patient management.
https://clinicaltrials.gov/ (NCT01843348; EudraCT number: 2011-005238-21).
非人类白细胞抗原(non-HLA)抗体,包括靶向血管紧张素 II 1 型受体(AT1R)和内皮素 1 A 型受体(ETAR)的抗体,是肾移植(KTx)领域的一个研究热点。这项探索性亚研究评估了依维莫司(EVR)或霉酚酸(MPA)联合他克莫司(TAC)或环孢素 A(CsA)对预先存在非 HLA 抗体、可能相关的排斥反应患者的影响,以及它们在 1 年时间里对肾功能的影响。
所有符合条件的患者在移植前被随机分为三组(1:1:1),分别接受 EVR/TAC、EVR/CsA 或 MPA/TAC 方案。在随机分组的 268 名患者中,对这些方案在肾移植术后一年内对非 HLA 抗体形成的影响以及与临床事件的关联进行了描述性评估。
在第 12 个月时,EVR/TAC 组中 AT1R 抗体和 ETAR 抗体阴性的患者发生率较高(分别为 82.2%和 76.7%),而 MPA/TAC 组中 AT1R 抗体和 ETAR 抗体阳性的发生率较高(分别为 28.1%和 34.7%)。非 HLA 抗体对任何治疗组的临床结局均无影响,且未报告移植肾丢失或死亡情况。
所研究的免疫抑制剂组合是安全的,对临床结局无影响,并提示减少钙调神经磷酸酶抑制剂的暴露量有助于更好地管理患者。
https://clinicaltrials.gov/(NCT01843348;欧盟临床试验编号:2011-005238-21)