申请人:INSERM (INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE)
公开号:US11298348B2
公开(公告)日:2022-04-12
Sarcoglycanopathies are autosomal recessive diseases caused by mutations in the one of the genes coding for any sarcoglycans (SG). The inventors previously showed that the application of small molecules developed to rescue ΔF508-CFTR trafficking, and known as CFTR correctors, improved the maturation of several α-sarcoglycan mutants that were consequently rescued at the plasma membrane (WO 014086687). Now, the inventors show that some specific CFTR correctors provide additive and even synergic effect when administered in combination.
肌糖蛋白病是一种常染色体隐性遗传病,由编码肌糖蛋白(SG)的一个基因突变引起。本发明人之前的研究表明,应用为挽救ΔF508-CFTR转运而开发的小分子(称为CFTR校正剂),可以改善几种α-肌糖突变体的成熟,从而在质膜上得到挽救(WO 014086687)。现在,本发明者证明,某些特定的 CFTR 校正器在联合使用时可产生叠加甚至协同效应。