Literature DB >> 34009038

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

Justin D Anderson1,2, Zhongyu Liu1,2, L Victoria Odom2, Latona Kersh1, Jennifer S Guimbellot1,2.   

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.

Entities:  

Keywords:  drug response; elexacaftor; ivacaftor; organoids; tezacaftor

Mesh:

Substances:

Year:  2021        PMID: 34009038      PMCID: PMC8321858          DOI: 10.1152/ajplung.00639.2020

Source DB:  PubMed          Journal:  Am J Physiol Lung Cell Mol Physiol        ISSN: 1040-0605            Impact factor:   6.011


  62 in total

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Journal:  J Cyst Fibros       Date:  2020-06-01       Impact factor: 5.482

Review 3.  Ivacaftor treatment of cystic fibrosis patients with the G551D mutation: a review of the evidence.

Authors:  Kavitha Kotha; John P Clancy
Journal:  Ther Adv Respir Dis       Date:  2013-09-03       Impact factor: 4.031

4.  Mutation-specific downregulation of CFTR2 variants by gating potentiators.

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6.  Mutations that permit residual CFTR function delay acquisition of multiple respiratory pathogens in CF patients.

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Journal:  Respir Res       Date:  2010-10-08

7.  Correction of CFTR function in intestinal organoids to guide treatment of cystic fibrosis.

Authors:  Anabela S Ramalho; Eva Fürstová; Annelotte M Vonk; Marc Ferrante; Catherine Verfaillie; Lieven Dupont; Mieke Boon; Marijke Proesmans; Jeffrey M Beekman; Ifat Sarouk; Carlos Vazquez Cordero; Francois Vermeulen; Kris De Boeck
Journal:  Eur Respir J       Date:  2021-01-05       Impact factor: 16.671

8.  Characterizing responses to CFTR-modulating drugs using rectal organoids derived from subjects with cystic fibrosis.

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9.  Potentiator ivacaftor abrogates pharmacological correction of ΔF508 CFTR in cystic fibrosis.

Authors:  Deborah M Cholon; Nancy L Quinney; M Leslie Fulcher; Charles R Esther; Jhuma Das; Nikolay V Dokholyan; Scott H Randell; Richard C Boucher; Martina Gentzsch
Journal:  Sci Transl Med       Date:  2014-07-23       Impact factor: 17.956

10.  Stratifying infants with cystic fibrosis for disease severity using intestinal organoid swelling as a biomarker of CFTR function.

Authors:  Karin M de Winter-de Groot; Hettie M Janssens; Rick T van Uum; Johanna F Dekkers; Gitte Berkers; Annelotte Vonk; Evelien Kruisselbrink; Hugo Oppelaar; Robert Vries; Hans Clevers; Roderick H J Houwen; Johanna C Escher; Sjoerd G Elias; Hugo R de Jonge; Yolanda B de Rijke; Harm A W M Tiddens; Cornelis K van der Ent; Jeffrey M Beekman
Journal:  Eur Respir J       Date:  2018-09-17       Impact factor: 16.671

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Review 2.  Established and novel human translational models to advance cystic fibrosis research, drug discovery, and optimize CFTR-targeting therapeutics.

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Review 4.  Advances in Preclinical In Vitro Models for the Translation of Precision Medicine for Cystic Fibrosis.

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Review 7.  Biological Models of the Lower Human Airways-Challenges and Special Requirements of Human 3D Barrier Models for Biomedical Research.

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  7 in total

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