Nephrology, Hemodialysis, Apheresis and Kidney Transplantation Department, University Hospital Grenoble, Grenoble, France.
University Grenoble Alpes, Grenoble, France.
Front Immunol. 2022 Apr 14;13:839380. doi: 10.3389/fimmu.2022.839380. eCollection 2022.
Chronic kidney disease (CKD) is a major public-health problem that increases the risk of end-stage kidney disease (ESKD), cardiovascular diseases, and other complications. Kidney transplantation is a renal-replacement therapy that offers better survival compared to dialysis. Antibody-mediated rejection (ABMR) is a significant complication following kidney transplantation: it contributes to both short- and long-term injury. The standard-of-care (SOC) therapy combines plasmapheresis and Intravenous Immunoglobulins (IVIg) with or without steroids, with or without rituximab: however, despite this combined treatment, ABMR remains the main cause of graft loss. IL-6 is a key cytokine: it regulates inflammation, and the development, maturation, and activation of T cells, B cells, and plasma cells. Tocilizumab (TCZ) is the main humanized monoclonal aimed at IL-6R and appears to be a safe and possible strategy to manage ABMR in sensitized recipients. We conducted a literature review to assess the place of the anti-IL-6R monoclonal antibody TCZ within ABMR protocols.
We systematically reviewed the PubMed literature and reviewed six studies that included 117 patients and collected data on the utilization of TCZ to treat ABMR.
Most studies report a significant reduction in levels of Donor Specific Antibodies (DSAs) and reduced inflammation and microvascular lesions (as found in biopsies). Stabilization of the renal function was observed. Adverse events were light to moderate, and mortality was not linked with TCZ treatment. The main side effect noted was infection, but infections did not occur more frequently in patients receiving TCZ as compared to those receiving SOC therapy.
TCZ may be an alternative to SOC for ABMR kidney-transplant patients, either as a first-line treatment or after failure of SOC. Further randomized and controlled studies are needed to support these results.
慢性肾脏病(CKD)是一个主要的公共卫生问题,增加了终末期肾病(ESKD)、心血管疾病和其他并发症的风险。肾移植是一种肾脏替代疗法,与透析相比,提供了更好的生存机会。抗体介导的排斥反应(ABMR)是肾移植后的一个重要并发症:它导致短期和长期损伤。标准治疗(SOC)包括血浆置换和静脉注射免疫球蛋白(IVIg),联合或不联合类固醇,联合或不联合利妥昔单抗:然而,尽管进行了这种联合治疗,ABMR 仍然是移植物丢失的主要原因。白细胞介素 6(IL-6)是一种关键的细胞因子:它调节炎症,以及 T 细胞、B 细胞和浆细胞的发育、成熟和激活。托珠单抗(TCZ)是主要的针对 IL-6R 的人源化单克隆抗体,似乎是一种安全且可能的策略,可用于管理致敏受者的 ABMR。我们进行了文献回顾,以评估抗 IL-6R 单克隆抗体 TCZ 在 ABMR 方案中的地位。
我们系统地回顾了 PubMed 文献,并回顾了六项研究,这些研究包括 117 名患者,并收集了使用 TCZ 治疗 ABMR 的数据。
大多数研究报告说,供体特异性抗体(DSAs)水平显著降低,炎症和微血管病变(如活检中所见)减少。肾功能稳定。观察到不良反应较轻至中度,死亡率与 TCZ 治疗无关。主要的副作用是感染,但与接受 SOC 治疗的患者相比,接受 TCZ 治疗的患者感染并不更频繁。
TCZ 可能是 ABMR 肾移植患者 SOC 的替代方案,无论是一线治疗还是 SOC 治疗失败后。需要进一步的随机对照研究来支持这些结果。