Efremova Anna, Kashirskaya Nataliya, Krasovskiy Stanislav, Melyanovskaya Yuliya, Krasnova Maria, Mokrousova Diana, Bulatenko Nataliya, Kondratyeva Elena, Makhnach Oleg, Bukharova Tatiana, Zinchenko Rena, Kutsev Sergey, Goldshtein Dmitry
Research Centre for Medical Genetics, Moscow 115522, Russia.
Moscow Regional Research and Clinical Institute ("MONIKI"), Moscow 129110, Russia.
Int J Mol Sci. 2024 Feb 27;25(5):2770. doi: 10.3390/ijms25052770.
p.Asn1303Lys (N1303K) is a common missense variant of the gene, causing cystic fibrosis (CF). In this study, we initially evaluated the influence of modulators on the restoration of N1303K- function using intestinal organoids derived from four CF patients expressing the N1303K variant. The forskolin-induced swelling assay in organoids offered valuable insights about the beneficial effects of VX-770 + VX-661 + VX-445 (Elexacaftor + Tezacaftor + Ivacaftor, ETI) on N1303K- function restoration and about discouraging the prescription of VX-770 + VX-809 (Ivacaftor + Lumacaftor) or VX-770 + VX-661 (Ivacaftor + Tezacaftor) therapy for N1303K/class I patients. Then, a comprehensive assessment was conducted on an example of one patient with the N1303K/class I genotype to examine the ETI effect on the restoration of N1303K- function using in vitro the patient's intestinal organoids, ex vivo the intestinal current measurements (ICM) method and assessment of the clinical status before and after targeted therapy. All obtained results are consistent with each other and have proven the effectiveness of ETI for the N1303K variant. ETI produced a significant positive effect on forskolin-induced swelling in N1303K/class I organoids indicating functional improvement of the protein; ICM demonstrated that ETI therapy restored function in the intestinal epithelium after three months of treatment, and the patient improved his clinical status and lung function, increased his body mass index (BMI) and reduced the lung pathogenic flora diversity, surprisingly without improving the sweat test results.
p.Asn1303Lys(N1303K)是该基因的一种常见错义变体,可导致囊性纤维化(CF)。在本研究中,我们最初使用来自四名表达N1303K变体的CF患者的肠道类器官,评估了调节剂对N1303K功能恢复的影响。类器官中福司可林诱导的肿胀试验提供了关于VX - 770 + VX - 661 + VX - 445(依列卡福妥 + 替扎卡福妥 + 依伐卡福妥,ETI)对N1303K功能恢复的有益作用以及不鼓励为N1303K/I类患者开具VX - 770 + VX - 809(依伐卡福妥 + 鲁马卡福妥)或VX - 770 + VX - 661(依伐卡福妥 + 替扎卡福妥)疗法的有价值见解。然后,以一名N1303K/I类基因型患者为例进行了全面评估,使用患者的肠道类器官在体外、肠道电流测量(ICM)方法在离体状态下以及评估靶向治疗前后的临床状态,来检查ETI对N1303K功能恢复的影响。所有获得的结果相互一致,并证明了ETI对N1303K变体的有效性。ETI对N1303K/I类类器官中福司可林诱导的肿胀产生了显著的积极影响,表明该蛋白质的功能得到改善;ICM表明,ETI治疗三个月后恢复了肠道上皮中的功能,患者的临床状态和肺功能得到改善,体重指数(BMI)增加,肺部致病菌群多样性降低,令人惊讶的是汗液测试结果并未改善。