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Development of highly potent glucocorticoids for steroid-resistant severe asthma.

Yuanzheng HeJingjing ShiQuang Tam NguyenErli YouHongbo LiuXin RenZhongshan WuJianshuang LiWenli QiuSok Kean KhooTao YangWei YiFeng SunZhijian XiXiaozhu HuangKarsten MelcherBooki MinH Eric Xu
Published in: Proceedings of the National Academy of Sciences of the United States of America (2019)
Clinical application of inhaled glucocorticoids (GCs) has been hampered in the case of steroid-resistant severe asthma. To overcome this limitation, we have developed a series of highly potent GCs, including VSGC12, VSG158, and VSG159 based on the structural insight into the glucocorticoid receptor (GR). Particularly, VSG158 exhibits a maximal repression of lung inflammation and is 10 times more potent than the currently most potent clinical GC, Fluticasone Furoate (FF), in a murine model of asthma. More importantly, VSG158 displays a unique property to reduce neutrophilic inflammation in a steroid-resistant airway inflammation model, which is refractory to clinically available GCs, including dexamethasone and FF. VSG158 and VSG159 are able to deliver effective treatments with reduced off-target and side effects. In addition, these GCs also display pharmacokinetic properties that are suitable for the inhalation delivery method for asthma treatment. Taken together, the excellent therapeutic and side-effect profile of these highly potent GCs holds promise for treating steroid-resistant severe asthma.
Keyphrases
  • anti inflammatory
  • oxidative stress
  • chronic obstructive pulmonary disease
  • lung function
  • cystic fibrosis
  • heart rate
  • air pollution
  • high resolution
  • replacement therapy