Durcan L, Petri M
Division of Rheumatology, University of Washington, Seattle, WA, USA.
Division of Rheumatology, Johns Hopkins University, School of Medicine, Baltimore, MD, USA
Lupus. 2016 Sep;25(10):1070-9. doi: 10.1177/0961203316652489.
Systemic lupus erythematosus (SLE) continues to have important morbidity and accelerated mortality despite therapeutic advances. Targeted therapies offer the possibility of improved efficacy with fewer side effects. Current management strategies rely heavily on nonspecific immunosuppressive agents. Prednisone, in particular, is responsible for a considerable burden of later organ damage. There are a multitude of diverse mechanisms of disease activity, immunogenic abnormalities and clinical manifestations to take into consideration in SLE. Many targeted agents with robust mechanistic preclinical data and promising early phase studies have ultimately been disappointing in phase III, randomized, controlled studies. Recent efforts have focused on B-cell therapies, in particular given the success of belimumab in clinical trials, with limited success. We remain optimistic regarding other specific therapies being evaluated, including interferon-alpha blockade. It is likely that in SLE, given the heterogeneity of the population involved, precision medicine is needed, rather than expecting that any single biologic will be universally effective.
尽管治疗取得了进展,但系统性红斑狼疮(SLE)仍然具有重要的发病率和加速的死亡率。靶向治疗提供了提高疗效且副作用更少的可能性。当前的管理策略严重依赖非特异性免疫抑制剂。特别是泼尼松,会导致相当大的后期器官损害负担。在SLE中,有多种不同的疾病活动机制、免疫原性异常和临床表现需要考虑。许多在临床前研究中有强大机制数据且早期研究前景良好的靶向药物,最终在III期随机对照研究中令人失望。最近的努力集中在B细胞疗法上,特别是鉴于贝利尤单抗在临床试验中的成功,但成效有限。我们对正在评估的其他特定疗法,包括α干扰素阻断疗法,仍持乐观态度。鉴于所涉及人群的异质性,在SLE中可能需要精准医学,而不是期望任何单一生物制剂都能普遍有效。