Institute for Drug Discovery, Faculty of Medicine, Leipzig University, Leipzig, Germany.
Department of Pharmaceutical Science, University of Basel, Basel, Switzerland.
Am J Hematol. 2023 May;98 Suppl 4:S82-S89. doi: 10.1002/ajh.26875.
Within a short few years, the number of complement inhibitors that are either approved for therapeutic application or evaluated in late-stage clinical trials has expanded remarkably. The sudden emergence of this target area in the pipelines of many biotech start-ups and even large pharmaceutical companies appears even more surprising when considering that the involvement of the complement system in various clinical conditions had long been recognized. In many aspects, however, the complement system is far from being a traditional drug target, which may explain the delayed breakthrough of this therapeutic strategy. While complement modulation is now considered an attractive "platform technology" with applications in a wide spectrum of disorders, the broad yet heterogeneous disease involvement of the complement system has long restricted its placement in traditional drug discovery programs. Concerns about the safety of complement-targeted interventions, the large number and high plasma concentrations of target proteins, and the complexity of the complement system's engagement in biological processes are among other factors that kept complement off the drug discovery radar for decades. Alongside technical advances and financial incentives, the innovation and persistence of academic and clinical researchers have been the critical driving force to navigate complement therapeutics out of the shadow into the spotlight. In this commentary, we document this remarkable development using select examples and aim to venture some predictions where this promising field may be headed to.
在短短几年内,无论是已获得治疗应用批准还是处于后期临床试验评估阶段的补体抑制剂数量都显著增加。当考虑到补体系统在各种临床情况下的参与早已被认识到,许多生物技术初创公司甚至大型制药公司的产品线中突然出现这一目标领域,就显得更加令人惊讶。然而,在许多方面,补体系统远非传统的药物靶点,这可能解释了这一治疗策略的延迟突破。虽然补体调节现在被认为是一种具有广泛应用潜力的“平台技术”,可应用于多种疾病,但补体系统广泛而复杂的疾病参与长期以来限制了其在传统药物发现项目中的定位。对补体靶向干预安全性的担忧、靶蛋白数量多且血浆浓度高以及补体系统在生物学过程中的参与的复杂性等因素,也是几十年来补体未被纳入药物发现雷达的原因。除了技术进步和资金激励外,学术和临床研究人员的创新和坚持是将补体疗法从幕后推向台前的关键推动力量。在这篇评论中,我们使用了一些例子来记录这一显著的发展,并尝试对这一充满希望的领域可能的发展方向进行一些预测。