Madanchi Nima, Bitzan Martin, Takano Tomoko
Division of Nephrology, Department of Medicine, McGill University Health Centre, Montreal, Quebec, Canada.
Division of Nephrology, Department of Pediatrics, Montreal Children's Hospital, McGill University Health Centre, Montreal, Quebec, Canada.
Can J Kidney Health Dis. 2017 Mar 13;4:2054358117698667. doi: 10.1177/2054358117698667. eCollection 2017.
Treatment with rituximab, a monoclonal antibody against the B-lymphocyte surface protein CD20, leads to the depletion of B cells. Recently, rituximab was reported to effectively prevent relapses of glucocorticoid-dependent or frequently relapsing minimal change disease (MCD). MCD is thought to be T-cell mediated; how rituximab controls MCD is not understood. In this review, we summarize key clinical studies demonstrating the efficacy of rituximab in idiopathic nephrotic syndrome, mainly MCD. We then discuss immunological features of this disease and potential mechanisms of action of rituximab in its treatment based on what is known about the therapeutic action of rituximab in other immune-mediated disorders. We believe that studies aimed at understanding the mechanisms of action of rituximab in MCD will provide a novel approach to resolve the elusive immune pathophysiology of MCD.
利妥昔单抗是一种针对B淋巴细胞表面蛋白CD20的单克隆抗体,使用该药物治疗会导致B细胞耗竭。最近,有报道称利妥昔单抗可有效预防糖皮质激素依赖型或频繁复发的微小病变肾病(MCD)的复发。MCD被认为是由T细胞介导的;利妥昔单抗如何控制MCD尚不清楚。在本综述中,我们总结了一些关键的临床研究,这些研究证明了利妥昔单抗在特发性肾病综合征(主要是MCD)中的疗效。然后,我们根据利妥昔单抗在其他免疫介导疾病中的治疗作用的已知情况,讨论该疾病的免疫学特征以及利妥昔单抗在其治疗中的潜在作用机制。我们认为,旨在了解利妥昔单抗在MCD中的作用机制的研究将为解决MCD难以捉摸的免疫病理生理学问题提供一种新方法。