Viklicky Ondrej, Zahradka Ivan, Mares Jan, Slatinska Janka, Parikova Alena, Petr Vojtech, Roder Matej, Jaklova Katerina, Osickova Klara, Janousek Libor, Hruba Petra
Department of Nephrology, Institute for Clinical and Experimental Medicine, Prague, Czechia.
Transplantation Laboratory, Institute for Clinical and Experimental Medicine, Prague, Czechia.
Transpl Int. 2025 May 19;38:14312. doi: 10.3389/ti.2025.14312. eCollection 2025.
Intravenous immunoglobulins (IVIG) are commonly used in peri-transplant desensitization, but evidence supporting their efficacy is limited. We conducted a prospective, randomized single-center, open-label, Phase IIIb non-inferiority clinical pilot trial to compare the efficacy of IVIG (administered at a dose of 3 × 0.5 g/kg) versus no IVIG, in conjunction with rabbit anti-thymocyte globulin (5-7 mg/kg) induction, in pre-sensitized patients with donor-specific antibodies who had negative pre-transplantation Flow- and CDC-crossmatches, between July 2020 and November 2022. The primary endpoint was the rate of efficacy failure, defined as biopsy-proven rejection within 12-month post-transplant. Secondary endpoints included the incidence of rejection at protocol biopsies, evaluated by histology and biopsy-based transcripts diagnostics. Of the screened patients, 53 (72.6%) were excluded due to crossmatch positivity. Ten patients were randomized to the IVIG+, and 7 to the IVIG-arm. The trial was prematurely terminated due to futility at interim analysis. In the IVIG-arm, 3 patients (43%) experienced the primary endpoint compared to none in the IVIG+ arm (p = 0.026). MMDx identified one molecular ABMR in the IVIG+ and 2 in the IVIG-arm in 12-month protocol biopsies. There was one graft loss in the IVIG-arm. The results of this pilot study, although not definitive, do not support the use of IVIG-sparing regimens in HLA-incompatible kidney transplantation (NCT04302805). This study is registered on ClinicalTrials.gov under the identifier NCT04302805.
静脉注射免疫球蛋白(IVIG)常用于移植围手术期脱敏治疗,但其疗效的证据有限。我们进行了一项前瞻性、随机、单中心、开放标签的IIIb期非劣效性临床试验,比较IVIG(剂量为3×0.5 g/kg)与不使用IVIG,联合兔抗胸腺细胞球蛋白(5 - 7 mg/kg)诱导治疗,在2020年7月至2022年11月期间,对移植前流式细胞术和补体依赖细胞毒性交叉配型阴性的预致敏供者特异性抗体患者的疗效。主要终点是疗效失败率,定义为移植后12个月内经活检证实的排斥反应。次要终点包括方案活检时排斥反应的发生率,通过组织学和基于活检的转录本诊断进行评估。在筛选的患者中,53例(72.6%)因交叉配型阳性被排除。10例患者被随机分配到IVIG+组,7例到IVIG-组。由于中期分析时无效,试验提前终止。在IVIG-组中,3例患者(43%)达到主要终点,而IVIG+组无一例(p = 0.026)。在12个月的方案活检中,MMDx在IVIG+组中识别出1例分子抗体介导的排斥反应,在IVIG-组中识别出2例。IVIG-组有1例移植肾丢失。这项初步研究的结果虽然不明确,但不支持在HLA不相合肾移植中使用不使用IVIG的方案(NCT04302805)。本研究已在ClinicalTrials.gov上注册,标识符为NCT04302805。