Department of Paediatrics, 2nd Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic; Department of Medical Microbiology, 2nd Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.
Department of Paediatrics, 2nd Faculty of Medicine, Charles University and Motol University Hospital, Prague, Czech Republic.
J Cyst Fibros. 2022 Mar;21(2):243-245. doi: 10.1016/j.jcf.2021.07.006. Epub 2021 Aug 2.
Superior efficacy of elexacaftor/tezacaftor/ivacaftor (ELX/TEZ/IVA) over tezacaftor/ivacaftor (TEZ/IVA) in people with cystic fibrosis (CF) and Phe508del/Phe508del genotype was shown in clinical trials. We utilized intestinal organoid approach to compare in vitro responses to these 2 CFTR modulator drug combinations and to check potential inter-individual variability in therapeutic response to the triple combination. Organoids from 17 subjects with Phe508del/Phe508del were screened with forskolin induced swelling assay. Significantly larger swelling, when exposed to ELX/TEZ/IVA as compared to TEZ/IVA, was observed in 16 of them. However, 1 sample showed no additional effect of ELX. The finding of unique CFTR variants in this sample indicates that genetic traits other than CF-causing CFTR mutation are worth exploring as they may have an impact on the definitive modulator drug response.
在囊性纤维化 (CF) 患者中,与 tezacaftor/ivacaftor (TEZ/IVA) 相比,elexacaftor/tezacaftor/ivacaftor (ELX/TEZ/IVA) 的疗效更优,且具有 Phe508del/Phe508del 基因型。在临床试验中已证实。我们利用肠类器官方法比较了这两种 CFTR 调节剂药物组合的体外反应,并检查了对三联药物治疗反应的潜在个体间差异。对 17 名 Phe508del/Phe508del 个体的类器官进行了 forskolin 诱导肿胀测定。与 TEZ/IVA 相比,16 名患者的类器官暴露于 ELX/TEZ/IVA 时出现了明显更大的肿胀。然而,有 1 个样本未显示出 ELX 的额外作用。该样本中独特的 CFTR 变体的发现表明,除 CF 引起的 CFTR 突变外,其他遗传特征值得探索,因为它们可能会对明确的调节剂药物反应产生影响。