Litcius/Paper detail

Forskolin induced swelling (FIS) assay in intestinal organoids to guide eligibility for compassionate use treatment in a CF patient with a rare genotype

Bente L. Aalbers, Jesse E. Brunsveld, Cornelis K. van der Ent, J.C. van den Eijnden, Jeffrey M. Beekman, Harry Heijerman

2022Journal of Cystic Fibrosis27 citationsDOIOpen Access PDF

Abstract

BACKGROUND: Forskolin-induced swelling of patient-derived organoids has been used to measure patient-specific CFTR function and CFTR modulator response. We present a case where CFTR function assessment in intestinal organoids was decisive for a patients' acceptance to a compassionate use program. CASE DESCRIPTION: A 56 years old female with cystic fibrosis compound heterozygous for F508del and a rare CFTR allele (c.3717+5G>T) experienced rapid clinical deterioration. The forskolin-induced swelling assay on her rectal organoids was used to confirm that the rare mutation is a minimal residual function mutation, and that other CFTR modulators would not likely be effective. Based on these two criteria and her clinical status, she was accepted for compassionate use of elexacaftor/tezacaftor/ivacaftor and showed improvement in all clinical parameters. CONCLUSIONS: This reports describes a first example that intestinal organoids were used to identify a previously unknown CFTR mutation as a minimal function mutation. The individual FIS-based definition of minimal residual function, response to ele/tez/iva and/or lack of response to other CFTR modulating drugs, may thus provide a tool for access to ele/tez/iva treatment for people with rare genotypes.

Topics & Concepts

IvacaftorCystic fibrosisMedicineMutationCystic fibrosis transmembrane conductance regulatorOrganoidNewborn screeningGenotypeCompound heterozygosityHeterozygote advantageInternal medicineGastroenterologyBiologyGeneticsGenePediatricsCystic Fibrosis Research AdvancesDigestive system and related healthNeonatal Respiratory Health Research
Forskolin induced swelling (FIS) assay in intestinal organoids to guide eligibility for compassionate use treatment in a CF patient with a rare genotype | Litcius