Ricklin Daniel, Barratt-Due Andreas, Mollnes Tom Eirik
Department of Pharmaceutical Sciences, University of Basel, Switzerland.
Department of Immunology, Oslo University Hospital, and K. G. Jebsen Inflammation Research Centre, University of Oslo, Norway; Department of Emergencies and Critical Care, Oslo University Hospital, Oslo, Norway.
Mol Immunol. 2017 Sep;89:10-21. doi: 10.1016/j.molimm.2017.05.013. Epub 2017 May 31.
Research during past decades made it evident that complement is involved in more tasks than fighting infections, but has important roles in other immune surveillance and housekeeping functions. If the balance between complement activation and regulation is out of tune, however, complement can quickly turn against the host and contribute to adverse processes that result in various clinical conditions. Whereas clinical awareness was initially focused on complement deficiencies, excessive activation and insufficient regulation are frequently the dominant factors in complement-related disorders. The individual complement profile of a patient often determines the course and severity of the disease, and the pathophysiological involvement of complement may be highly diverse. As a consequence, complement assays have evolved as essential tools not only in initial diagnosis but also for following disease progression and for monitoring complement-targeted therapies, which become increasingly available in routine clinical use. We herein review the current state of complement-directed drug candidates in clinical evaluation and provide an overview of extended indications considered for the FDA-approved inhibitor eculizumab. Furthermore we review the literature describing cases reports and case series where eculizumab has been used "off-label". Finally, we give a summary of the currently available tests to measure complement profiles and discuss their suitability in diagnostics and treatment monitoring. With complement finally entering the clinical arena, there are intriguing opportunities for treating complement-mediated diseases. However, this progress also requires a new awareness about complement pathophysiology, adequate diagnostic tools and suitable treatment options among clinicians treating patients with such disorders.
过去几十年的研究表明,补体参与的任务远不止对抗感染,还在其他免疫监视和维持机体正常功能方面发挥重要作用。然而,如果补体激活与调节之间的平衡失调,补体可能会迅速转而攻击宿主,引发导致各种临床病症的不良过程。尽管临床关注最初集中在补体缺陷上,但补体过度激活和调节不足往往是补体相关疾病的主要因素。患者的个体补体特征通常决定疾病的进程和严重程度,补体的病理生理参与情况可能高度多样。因此,补体检测不仅已成为初始诊断的重要工具,还用于跟踪疾病进展以及监测针对补体的治疗,这类治疗在常规临床应用中越来越普遍。我们在此回顾了处于临床评估阶段的补体靶向候选药物的现状,并概述了FDA批准的抑制剂依库珠单抗所考虑的扩展适应症。此外,我们还回顾了描述依库珠单抗“超说明书”使用的病例报告和病例系列的文献。最后,我们总结了目前可用于测量补体特征的检测方法,并讨论了它们在诊断和治疗监测中的适用性。随着补体最终进入临床领域,治疗补体介导疾病的机会令人期待。然而,这一进展也要求治疗此类疾病患者的临床医生对补体病理生理学有新的认识,具备足够的诊断工具和合适的治疗选择。