He Yuanzheng, Shi Jingjing, Yi Wei, Ren Xin, Gao Xiang, Li Jianshuang, Wu Nanyan, Weaver Kevin, Xie Qian, Khoo Sok Kean, Yang Tao, Huang Xiaozhu, Melcher Karsten, Xu H Eric
Laboratory of Structural Sciences, Van Andel Research Institute, 333 Bostwick Avenue Northeast, Grand Rapids, MI, USA.
VARI-SIMM Center, Center for Structure and Function of Drug Targets, Key Laboratory of Receptor Research, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai, China.
Cell Discov. 2015;1:15035-. doi: 10.1038/celldisc.2015.35. Epub 2015 Dec 15.
Glucocorticoids are the most effective treatment for asthma. However, their clinical applications are limited by low efficacy in severe asthma and by undesired side effects associated with high dose or prolonged use. The most successful approach to overcome these limitations has been the development of highly potent glucocorticoids that can be delivered to the lungs by inhalation to achieve local efficacy with minimal systemic effects. On the basis of our previous structural studies, we designed and developed a highly potent glucocorticoid, VSGC12, which showed an improved anti-inflammation activity in both cell-based reporter assays and cytokine inhibition experiments, as well as in a gene expression profiling of mouse macrophage RAW264.7 cells. In a mouse asthma model, VSGC12 delivered a higher efficacy than fluticasone furoate, a leading clinical compound, in many categories including histology and the number of differentiated immune cells. VSGC12 also showed a higher potency than fluticasone furoate in repressing most asthma symptoms. Finally, VSGC12 showed a better side effect profile than fluticasone furoate at their respective effective doses, including better insulin response and less bone loss in an animal model. The excellent therapeutic and side effect properties of VSGC12 provide a promising perspective for developing this potent glucocorticoid as a new effective drug for asthma.
糖皮质激素是治疗哮喘最有效的药物。然而,它们的临床应用受到严重哮喘疗效低以及高剂量或长期使用相关不良副作用的限制。克服这些限制最成功的方法是开发高效能的糖皮质激素,可通过吸入方式递送至肺部,以实现局部疗效且全身影响最小。基于我们之前的结构研究,我们设计并开发了一种高效能的糖皮质激素VSGC12,其在基于细胞的报告基因检测、细胞因子抑制实验以及小鼠巨噬细胞RAW264.7细胞的基因表达谱分析中均显示出增强的抗炎活性。在小鼠哮喘模型中,VSGC12在包括组织学和分化免疫细胞数量等多个类别中比临床常用药物糠酸氟替卡松具有更高的疗效。VSGC12在抑制大多数哮喘症状方面也比糠酸氟替卡松具有更高的效能。最后,在各自的有效剂量下,VSGC12比糠酸氟替卡松表现出更好的副作用特征,包括在动物模型中具有更好的胰岛素反应和更少的骨质流失。VSGC12出色的治疗和副作用特性为将这种高效能糖皮质激素开发为治疗哮喘的新型有效药物提供了广阔前景。