Suppr超能文献

囊性纤维化跨膜传导调节因子(CFTR)功能和对调节剂的临床反应与鼻上皮类器官肿胀呈平行关系。

CFTR function and clinical response to modulators parallel nasal epithelial organoid swelling.

机构信息

Gregory Fleming James Cystic Fibrosis Research Center, University of Alabama at Birmingham, Birmingham, Alabama.

Division of Pulmonary and Sleep Medicine, Department of Pediatrics, University of Alabama at Birmingham, Birmingham, Alabama.

出版信息

Am J Physiol Lung Cell Mol Physiol. 2021 Jul 1;321(1):L119-L129. doi: 10.1152/ajplung.00639.2020. Epub 2021 May 19.

Abstract

In vitro biomarkers to assess cystic fibrosis transmembrane conductance regulator activity are desirable for precision modulator selection and as a tool for clinical trials. Here, we describe an organoid swelling assay derived from human nasal epithelia using commercially available reagents and equipment and an automated imaging process. Cells were collected in nasal brush biopsies, expanded in vitro, and cultured as spherical organoids or as monolayers. Organoids were used in a functional swelling assay with automated measurements and analysis, whereas monolayers were used for short-circuit current measurements to assess ion channel activity. Clinical data were collected from patients on modulators. Relationships between swelling data and short-circuit current, as well as between swelling data and clinical outcome measures, were assessed. The organoid assay measurements correlated with short-circuit current measurements for ion channel activity. The functional organoid assay distinguished individual responses as well as differences between groups. The organoid assay distinguished incremental drug responses to modulator monotherapy with ivacaftor and combination therapy with ivacaftor, tezacaftor, and elexacaftor. The swelling activity paralleled the clinical response. In conclusion, an in vitro biomarker derived from patients' cells can be used to predict responses to drugs and is likely to be useful as a preclinical tool to aid in the development of novel treatments and as a clinical trial outcome measure for a variety of applications, including gene therapy or editing.

摘要

评估囊性纤维化跨膜电导调节剂活性的体外生物标志物是精准调节剂选择的理想工具,也是临床试验的工具。在这里,我们描述了一种源自人鼻上皮的类器官肿胀测定法,该方法使用市售试剂和设备以及自动化成像过程。细胞从鼻刷活检中收集,在体外扩增,并培养为球形类器官或单层。使用自动化测量和分析的功能性肿胀测定法对类器官进行测试,而使用单层进行评估离子通道活性的短路电流测量。从接受调节剂治疗的患者中收集临床数据。评估肿胀数据与短路电流之间的关系,以及肿胀数据与临床结果测量之间的关系。类器官测定的测量结果与离子通道活性的短路电流测量结果相关。功能性类器官测定法区分了个体反应以及组间差异。类器官测定法区分了伊伐卡托单药治疗和伊伐卡托、特扎卡托和埃利卡托联合治疗的增量药物反应。肿胀活性与临床反应平行。总之,源自患者细胞的体外生物标志物可用于预测对药物的反应,并且可能作为一种临床前工具,有助于开发新的治疗方法,并作为各种应用的临床试验结果测量指标,包括基因治疗或编辑。

相似文献

1
CFTR function and clinical response to modulators parallel nasal epithelial organoid swelling.
Am J Physiol Lung Cell Mol Physiol. 2021 Jul 1;321(1):L119-L129. doi: 10.1152/ajplung.00639.2020. Epub 2021 May 19.
2
Elexacaftor/Ivacaftor/Tezacaftor: First Approval.
Drugs. 2019 Dec;79(18):2001-2007. doi: 10.1007/s40265-019-01233-7.
3
Response to elexacaftor/tezacaftor/ivacaftor in intestinal organoids derived from people with cystic fibrosis.
J Cyst Fibros. 2022 Mar;21(2):243-245. doi: 10.1016/j.jcf.2021.07.006. Epub 2021 Aug 2.
6
CFTR modulators response of S737F and T465N CFTR variants on patient-derived rectal organoids.
Orphanet J Rare Dis. 2024 Sep 13;19(1):343. doi: 10.1186/s13023-024-03334-3.
7
VX-445-Tezacaftor-Ivacaftor in Patients with Cystic Fibrosis and One or Two Phe508del Alleles.
N Engl J Med. 2018 Oct 25;379(17):1612-1620. doi: 10.1056/NEJMoa1807120. Epub 2018 Oct 18.
9
Net benefit of ivacaftor during prolonged tezacaftor/elexacaftor exposure in vitro.
J Cyst Fibros. 2022 Jul;21(4):637-643. doi: 10.1016/j.jcf.2022.02.011. Epub 2022 Mar 2.

引用本文的文献

1
Organoid-on-a-chip (OrgOC): Advancing cystic fibrosis research.
Mater Today Bio. 2025 Jul 28;34:102148. doi: 10.1016/j.mtbio.2025.102148. eCollection 2025 Oct.
3
Druggable redox pathways against Mycobacterium abscessus in cystic fibrosis patient-derived airway organoids.
PLoS Pathog. 2023 Aug 24;19(8):e1011559. doi: 10.1371/journal.ppat.1011559. eCollection 2023 Aug.
4
Post-approval studies with the CFTR modulators Elexacaftor-Tezacaftor-Ivacaftor.
Front Pharmacol. 2023 Mar 21;14:1158207. doi: 10.3389/fphar.2023.1158207. eCollection 2023.
6
Measuring cystic fibrosis drug responses in organoids derived from 2D differentiated nasal epithelia.
Life Sci Alliance. 2022 Aug 3;5(12):e202101320. doi: 10.26508/lsa.202101320.
8
A year in review: Real world evidence, functional monitoring and emerging therapeutics in 2021.
J Cyst Fibros. 2022 Mar;21(2):191-196. doi: 10.1016/j.jcf.2022.02.014. Epub 2022 Mar 7.
9
Culture and Imaging of Human Nasal Epithelial Organoids.
J Vis Exp. 2021 Dec 17(178). doi: 10.3791/63064.

本文引用的文献

1
Correction of CFTR function in intestinal organoids to guide treatment of cystic fibrosis.
Eur Respir J. 2021 Jan 5;57(1). doi: 10.1183/13993003.02426-2019. Print 2021 Jan.
2
Accumulation and persistence of ivacaftor in airway epithelia with prolonged treatment.
J Cyst Fibros. 2020 Sep;19(5):746-751. doi: 10.1016/j.jcf.2020.04.010. Epub 2020 Jun 11.
4
Human Nasal Epithelial Organoids for Therapeutic Development in Cystic Fibrosis.
Genes (Basel). 2020 May 29;11(6):603. doi: 10.3390/genes11060603.
6
Personalised medicine for non-classic cystic fibrosis resulting from rare CFTR mutations.
Eur Respir J. 2020 Jul 30;56(1). doi: 10.1183/13993003.00062-2020. Print 2020 Jul.
7
Variable cellular ivacaftor concentrations in people with cystic fibrosis on modulator therapy.
J Cyst Fibros. 2020 Sep;19(5):742-745. doi: 10.1016/j.jcf.2020.01.011. Epub 2020 Feb 7.
8
Intestinal organoids for Cystic Fibrosis research.
J Cyst Fibros. 2020 Mar;19 Suppl 1:S60-S64. doi: 10.1016/j.jcf.2019.11.002. Epub 2019 Nov 28.
10
Elexacaftor-Tezacaftor-Ivacaftor for Cystic Fibrosis with a Single Phe508del Allele.
N Engl J Med. 2019 Nov 7;381(19):1809-1819. doi: 10.1056/NEJMoa1908639. Epub 2019 Oct 31.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验