de Poel Eyleen, Spelier Sacha, Korporaal Ricardo, Lai Ka Wai, Boj Sylvia F, Conrath Katja, van der Ent Cornelis K, Beekman Jeffrey M
Department of Pediatric Respiratory Medicine, Wilhelmina Children's Hospital, University Medical Center, Utrecht University, Utrecht, Netherlands.
Regenerative Medicine Utrecht, University Medical Center, Utrecht University, Utrecht, Netherlands.
Front Mol Biosci. 2021 Sep 15;8:698358. doi: 10.3389/fmolb.2021.698358. eCollection 2021.
Cystic fibrosis transmembrane conductance regulator (CFTR) modulators have transformed the treatment of cystic fibrosis (CF) by targeting the basis of the disease. In particular, treatment regimen consisting of multiple compounds with complementary mechanisms of action have been shown to result in optimal efficacy. Here, we assessed the efficacy of combinations of the CFTR modulators ABBV/GLPG-2222, GLPG/ABBV-2737 and ABBV/GLPG-2451, and compared it to VX-770/VX-809 in 28 organoid lines heterozygous for F508del allele and a class I mutation and seven homozygous F508del organoid lines. The combination ABBV/GLPG-2222/ABBV-2737/ABBV/GLPG-2451 showed increased efficacy over VX-770/VX-809 for most organoids, despite considerable variation in efficacy between the different organoid cultures. These differences in CFTR restoration between organoids with comparable genotypes underline the relevance of continuing to optimize the ABBV/GLPG-Triple therapy, as well as the in vitro characterization of efficacy in clinically relevant models.
囊性纤维化跨膜传导调节因子(CFTR)调节剂通过针对疾病根源改变了囊性纤维化(CF)的治疗方式。特别是,由具有互补作用机制的多种化合物组成的治疗方案已显示出最佳疗效。在此,我们评估了CFTR调节剂ABBV/GLPG - 2222、GLPG/ABBV - 2737和ABBV/GLPG - 2451组合的疗效,并在28个F508del等位基因杂合且伴有I类突变的类器官系以及7个纯合F508del类器官系中,将其与VX - 770/VX - 809进行比较。尽管不同类器官培养物之间的疗效存在相当大的差异,但ABBV/GLPG - 2222/ABBV - 2737/ABBV/GLPG - 2451组合对大多数类器官显示出比VX - 770/VX - 809更高的疗效。具有可比基因型的类器官之间CFTR恢复的这些差异强调了继续优化ABBV/GLPG三联疗法以及在临床相关模型中进行疗效体外表征的相关性。