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...
Autores principales: | , , , , , , , , , , , , , |
---|---|
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 |