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.

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.

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

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aminophenols / pharmacology*
  • Benzodioxoles / pharmacology*
  • Case-Control Studies
  • Chloride Channel Agonists / pharmacology
  • Cystic Fibrosis / drug therapy
  • Cystic Fibrosis / metabolism*
  • Cystic Fibrosis / pathology
  • Cystic Fibrosis Transmembrane Conductance Regulator / genetics
  • Cystic Fibrosis Transmembrane Conductance Regulator / metabolism*
  • Humans
  • Indoles / pharmacology*
  • Ion Transport
  • Mutation
  • Nasal Mucosa / drug effects
  • Nasal Mucosa / metabolism*
  • Organoids / drug effects
  • Organoids / metabolism
  • Pyrazoles / pharmacology*
  • Pyridines / pharmacology*
  • Pyrrolidines / pharmacology*
  • Quinolones / pharmacology*

Substances

  • Aminophenols
  • Benzodioxoles
  • CFTR protein, human
  • Chloride Channel Agonists
  • Indoles
  • Pyrazoles
  • Pyridines
  • Pyrrolidines
  • Quinolones
  • tezacaftor
  • Cystic Fibrosis Transmembrane Conductance Regulator
  • ivacaftor
  • elexacaftor

Associated data

  • figshare/10.6084/m9.figshare.13497210.v1