Department of Medicine, University of Louisville School of Medicine, Louisville, KY.
Department of Medicine, University of Louisville School of Medicine, Louisville, KY.
Adv Chronic Kidney Dis. 2019 Sep;26(5):351-359. doi: 10.1053/j.ackd.2019.09.001.
Lupus nephritis (LN) occurs in up to 60% of SLE patients, and is a leading cause of disability and death. Current treatment of LN consists of a combination of high dose corticosteroids that non-specifically decrease inflammation and cytotoxic medications that reduce auto-antibody production. That combination of therapy is associated with significant side effects while remission rates remain inadequate. Since the introduction of biologics into the pharmacological armamentarium, there has been hope for less toxic and more effective therapies for LN. Unfortunately, after multiple clinical trials, no biologic has improved efficacy over standard of care therapies for LN. This is likely, in part, due to disease heterogeneity. The utilization of biomarkers in LN may provide a way to stratify patients and guide therapeutic options. In this review, we summarize traditional and novel LN biomarkers and discuss how they may be used to diagnose, stratify, and guide therapy in patients with LN, bringing precision medicine to the forefront of LN therapy.
狼疮肾炎(LN)可发生于高达 60%的系统性红斑狼疮(SLE)患者中,是导致残疾和死亡的主要原因。目前 LN 的治疗包括大剂量皮质类固醇的联合应用,其可非特异性地减轻炎症,以及细胞毒性药物,可减少自身抗体的产生。该联合治疗方案与显著的副作用相关,而缓解率仍然不足。自从生物制剂引入到药理学武器库中以来,人们一直希望为 LN 提供毒性更小、更有效的治疗方法。不幸的是,经过多次临床试验,没有一种生物制剂在 LN 的治疗效果上优于标准治疗方法。这可能部分归因于疾病异质性。LN 生物标志物的应用可能为患者分层和指导治疗选择提供一种方法。在这篇综述中,我们总结了传统和新型 LN 生物标志物,并讨论了它们如何用于诊断、分层和指导 LN 患者的治疗,将精准医学推向 LN 治疗的前沿。