Cargando…

Validating organoid-derived human intestinal monolayers for personalized therapy in cystic fibrosis

Highly effective drugs modulating the defective protein encoded by the CFTR gene have revolutionized cystic fibrosis (CF) therapy. Preclinical drug-testing on human nasal epithelial (HNE) cell cultures and 3-dimensional human intestinal organoids (3D HIO) are used to address patient-specific variati...

Descripción completa

Detalles Bibliográficos
Autores principales: Birimberg-Schwartz, Liron, Ip, Wan, Bartlett, Claire, Avolio, Julie, Vonk, Annelotte M, Gunawardena, Tarini, Du, Kai, Esmaeili, Mohsen, Beekman, Jeffrey M, Rommens, Johanna, Strug, Lisa, Bear, Christine E, Moraes, Theo J, Gonska, Tanja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Life Science Alliance LLC 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10079552/
https://www.ncbi.nlm.nih.gov/pubmed/37024122
http://dx.doi.org/10.26508/lsa.202201857
_version_ 1785020749289881600
author Birimberg-Schwartz, Liron
Ip, Wan
Bartlett, Claire
Avolio, Julie
Vonk, Annelotte M
Gunawardena, Tarini
Du, Kai
Esmaeili, Mohsen
Beekman, Jeffrey M
Rommens, Johanna
Strug, Lisa
Bear, Christine E
Moraes, Theo J
Gonska, Tanja
author_facet Birimberg-Schwartz, Liron
Ip, Wan
Bartlett, Claire
Avolio, Julie
Vonk, Annelotte M
Gunawardena, Tarini
Du, Kai
Esmaeili, Mohsen
Beekman, Jeffrey M
Rommens, Johanna
Strug, Lisa
Bear, Christine E
Moraes, Theo J
Gonska, Tanja
author_sort Birimberg-Schwartz, Liron
collection PubMed
description Highly effective drugs modulating the defective protein encoded by the CFTR gene have revolutionized cystic fibrosis (CF) therapy. Preclinical drug-testing on human nasal epithelial (HNE) cell cultures and 3-dimensional human intestinal organoids (3D HIO) are used to address patient-specific variation in drug response and to optimize individual treatment for people with CF. This study is the first to report comparable CFTR functional responses to CFTR modulator treatment among patients with different classes of CFTR gene variants using the three methods of 2D HIO, 3D HIO, and HNE. Furthermore, 2D HIO showed good correlation to clinical outcome markers. A larger measurable CFTR functional range and access to the apical membrane were identified as advantages of 2D HIO over HNE and 3D HIO, respectively. Our study thus expands the utility of 2D intestinal monolayers as a preclinical drug testing tool for CF.
format Online
Article
Text
id pubmed-10079552
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Life Science Alliance LLC
record_format MEDLINE/PubMed
spelling pubmed-100795522023-04-08 Validating organoid-derived human intestinal monolayers for personalized therapy in cystic fibrosis Birimberg-Schwartz, Liron Ip, Wan Bartlett, Claire Avolio, Julie Vonk, Annelotte M Gunawardena, Tarini Du, Kai Esmaeili, Mohsen Beekman, Jeffrey M Rommens, Johanna Strug, Lisa Bear, Christine E Moraes, Theo J Gonska, Tanja Life Sci Alliance Research Articles Highly effective drugs modulating the defective protein encoded by the CFTR gene have revolutionized cystic fibrosis (CF) therapy. Preclinical drug-testing on human nasal epithelial (HNE) cell cultures and 3-dimensional human intestinal organoids (3D HIO) are used to address patient-specific variation in drug response and to optimize individual treatment for people with CF. This study is the first to report comparable CFTR functional responses to CFTR modulator treatment among patients with different classes of CFTR gene variants using the three methods of 2D HIO, 3D HIO, and HNE. Furthermore, 2D HIO showed good correlation to clinical outcome markers. A larger measurable CFTR functional range and access to the apical membrane were identified as advantages of 2D HIO over HNE and 3D HIO, respectively. Our study thus expands the utility of 2D intestinal monolayers as a preclinical drug testing tool for CF. Life Science Alliance LLC 2023-04-04 /pmc/articles/PMC10079552/ /pubmed/37024122 http://dx.doi.org/10.26508/lsa.202201857 Text en © 2023 Birimberg-Schwartz et al. https://creativecommons.org/licenses/by/4.0/This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Articles
Birimberg-Schwartz, Liron
Ip, Wan
Bartlett, Claire
Avolio, Julie
Vonk, Annelotte M
Gunawardena, Tarini
Du, Kai
Esmaeili, Mohsen
Beekman, Jeffrey M
Rommens, Johanna
Strug, Lisa
Bear, Christine E
Moraes, Theo J
Gonska, Tanja
Validating organoid-derived human intestinal monolayers for personalized therapy in cystic fibrosis
title Validating organoid-derived human intestinal monolayers for personalized therapy in cystic fibrosis
title_full Validating organoid-derived human intestinal monolayers for personalized therapy in cystic fibrosis
title_fullStr Validating organoid-derived human intestinal monolayers for personalized therapy in cystic fibrosis
title_full_unstemmed Validating organoid-derived human intestinal monolayers for personalized therapy in cystic fibrosis
title_short Validating organoid-derived human intestinal monolayers for personalized therapy in cystic fibrosis
title_sort validating organoid-derived human intestinal monolayers for personalized therapy in cystic fibrosis
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10079552/
https://www.ncbi.nlm.nih.gov/pubmed/37024122
http://dx.doi.org/10.26508/lsa.202201857
work_keys_str_mv AT birimbergschwartzliron validatingorganoidderivedhumanintestinalmonolayersforpersonalizedtherapyincysticfibrosis
AT ipwan validatingorganoidderivedhumanintestinalmonolayersforpersonalizedtherapyincysticfibrosis
AT bartlettclaire validatingorganoidderivedhumanintestinalmonolayersforpersonalizedtherapyincysticfibrosis
AT avoliojulie validatingorganoidderivedhumanintestinalmonolayersforpersonalizedtherapyincysticfibrosis
AT vonkannelottem validatingorganoidderivedhumanintestinalmonolayersforpersonalizedtherapyincysticfibrosis
AT gunawardenatarini validatingorganoidderivedhumanintestinalmonolayersforpersonalizedtherapyincysticfibrosis
AT dukai validatingorganoidderivedhumanintestinalmonolayersforpersonalizedtherapyincysticfibrosis
AT esmaeilimohsen validatingorganoidderivedhumanintestinalmonolayersforpersonalizedtherapyincysticfibrosis
AT beekmanjeffreym validatingorganoidderivedhumanintestinalmonolayersforpersonalizedtherapyincysticfibrosis
AT rommensjohanna validatingorganoidderivedhumanintestinalmonolayersforpersonalizedtherapyincysticfibrosis
AT struglisa validatingorganoidderivedhumanintestinalmonolayersforpersonalizedtherapyincysticfibrosis
AT bearchristinee validatingorganoidderivedhumanintestinalmonolayersforpersonalizedtherapyincysticfibrosis
AT moraestheoj validatingorganoidderivedhumanintestinalmonolayersforpersonalizedtherapyincysticfibrosis
AT gonskatanja validatingorganoidderivedhumanintestinalmonolayersforpersonalizedtherapyincysticfibrosis