| Literature DB >> 30894497 |
Yuanzheng He1,2, Jingjing Shi3, Quang Tam Nguyen4, Erli You3, Hongbo Liu5, Xin Ren6, Zhongshan Wu7, Jianshuang Li8, Wenli Qiu6, Sok Kean Khoo9, Tao Yang8, Wei Yi10,11,12, Feng Sun7, Zhijian Xi7, Xiaozhu Huang6, Karsten Melcher2, Booki Min13, H Eric Xu14,3.
Abstract
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.Entities:
Keywords: VSG158; VSG159; glucocorticoid; high potency; steroid-resistant asthma
Mesh:
Substances:
Year: 2019 PMID: 30894497 PMCID: PMC6452690 DOI: 10.1073/pnas.1816734116
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205