Azzaoui Kamal, Blommers Marcel, Götte Marjo, Zimmermann Kaspar, Liu He, Fretz Heinz
Saverna Therapeutics AG, Pumpmattenweg 3 CH-4105 Biel-Benken, Switzerland;, Email:
Saverna Therapeutics AG, Pumpmattenweg 3 CH-4105 Biel-Benken, Switzerland.
Chimia (Aarau). 2020 Oct 28;74(10):798-802. doi: 10.2533/chimia.2020.798.
Systemic lupus erythematosus (SLE) is an autoimmune disease that often leads to functional disorder in multiple organs, most often with symptoms related to skin lesions, cardiovascular disease and kidney damage. Although significant efforts have been made to find efficient therapies, it still remains uncured. Furthermore, the current therapy is often associated with adverse side effects and leads to a high economic burden for society. At Saverna Therapeutics, in collaboration with our partners, we initiated a lead discovery program that aims to modulate the biogenesis of miR-155. This non-coding RNA is upregulated in SLE patients and SLE mouse models. We used our drug discovery platform based on iterative fragment-based screening by nuclear magnetic resonance (NMR) and machine learning to identify ligands of pre-miR-155. After several iterations and chemical modifications, we have identified compounds that show structure-activity relationships in cellular assays. These inhibitors reduced the level of miR-155 as well as its associated inflammatory protein TNF α whereas the cells remained viable during exposure of the compounds.
系统性红斑狼疮(SLE)是一种自身免疫性疾病,常导致多器官功能紊乱,最常见的症状与皮肤病变、心血管疾病和肾损伤有关。尽管人们已经做出了巨大努力来寻找有效的治疗方法,但该疾病仍然无法治愈。此外,目前的治疗方法常常伴有不良副作用,并给社会带来高昂的经济负担。在Saverna Therapeutics公司,我们与合作伙伴共同启动了一项先导化合物发现计划,旨在调节miR-155的生物合成。这种非编码RNA在SLE患者和SLE小鼠模型中表达上调。我们利用基于核磁共振(NMR)和机器学习的迭代片段筛选药物发现平台,来识别前体miR-155的配体。经过多次迭代和化学修饰,我们已经鉴定出在细胞试验中显示出构效关系的化合物。这些抑制剂降低了miR-155及其相关炎症蛋白TNFα的水平,而在化合物处理期间细胞仍保持存活。