University Hospital of Montpellier, Arnaud de Villeneuve Hospital
Montpellier, Hérault, 34295, France
Location status: Recruiting
NCT Number: NCT06755008
The aim of this interventional, cross-sectional and pathophysiological experimental study is to evaluate the potential of a patient's induced pluripotent stem (iPS) cells, used prior to the re-differentiation stage, to enable ex vivo repair of the injured epithelium in patients with chronic obstructive pulmonary disease (COPD), smokers without COPD and non-smoking controls.
The main questions it aims to answer are:
* to evaluate the repair capacity of bronchial epithelium in COPD subjects, using a model of bronchial epithelium reconstituted in air/liquid interface culture and the iPS model. * epithelia repair capacities in normal or aberrant situations, as well as the time required for this repair, and to determine the involvement of grafted iPS cells in epithelia repair in cultured control subjects, smokers without COPD and COPD patients.
Researchers will compare 3 groups of participants (COPD patients, smokers without COPD and non-smokers without COPD) for epithelial repair efficacy between non-grafted ALI cultures and ALI cultures grafted with iPS cells, in order to assess their contribution to epithelial repair.
Participants will undergo a bronchial fibroscopy (for clinical indications) with two additional biopsies specific to the study.
This research could lead to breakthroughs in cell-based therapies for COPD, with long-term implications for epigenetic treatments and in vivo applications.
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
Montpellier, Hérault, 34295, France
Location status: Recruiting
Recently, the research team were able to show that there is a deficiency in a particular subtype of club cells destined to become ciliated in COPD, which would explain the inversion of the ciliated cell/caliciform cell ratio and therefore in the formation of the mucous plugs involved in bronchiolar obstruction.
iPS (induced pluripotent stem cells) represent a major biological breakthrough that has been awarded a Nobel Prize. They offer the advantage of being pluripotent, capable of multiplying endlessly, and thus of differentiating into any other cell type, or even organ, in short, embryogenesis. Researchers have developed a protocol for differentiating iPS cells into bronchial epithelia, with interesting success. These epithelia reconstituted in an air-liquid interface (iALI) reproduce all the characteristics of epithelia in vivo, in particular with the presence of all cell subtypes.
The research team hypothesizes that a patient's iPS cells, used before the re-differentiation stage, will enable ex vivo repair of his damaged epithelium.
The expected results of this project will be to validate the in vitro model of epithelial cell aggression in air-liquid interface (ALI) cultures, and to determine the feasibility of seeding iPS-derived epithelial cells. ALI epithelia from COPD patients would repair better or even normally thanks to iPS.
Ultimately, this project could be a potential therapy targeting epigenetics, and why not a cell therapy.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
General Inclusion Criteria
Group 1 Inclusion Criteria: COPD
Group 2 Inclusion Criteria: Smokers without COPD (n=10)
Group 3 Inclusion Criteria: Non-smoker controls (n=10)
Exclusion criteria
2 bronchial biopsies will be taken during bronchial fibroscopy
Time frame: Day 1
Percentage of repair at 24 hours post-lesion of ALI cultures vs. the same ALI cultures "grafted with iPS". This percentage will be determined by the surface area of the culture reconstructed after scratching divided by the surface area initially scratched.
Time frame: Day 2, Day 3 and day 7
Calculation of the percentage of repair at 48 hours, 72 hours and at 7 days post-scratch. This percentage will be determined by the surface area of the culture rebuilt after scratching divided by the surface area initially scratched.
Time frame: Day 2, Day 3 and day 7
Verification of the integrity of the bronchial epithelium obtained by measuring the transepithelial electrical resistance. (expressed as Ω/cm2 at each time point).
Time frame: Day 2, Day 3 and day 7
Cell density measurements (% GFP cells/total cells) by microscopy at each time point
Time frame: Day 2, Day 3 and day 7
immunofluorescence will be used to assess the density of basal, club, ciliated and caliciform cells; the release of key proinflammatory cytokines classically implicated in COPD will be assayed in the supernatant of these cultures.
Time frame: Day 2, Day 3 and day 7
Comparison of the transcriptomic profile by ANOVA analysis of the 10 most highly expressed genes between native cells and IPS cells.
Time frame: Day 2, Day 3 and day 7
Comparison of the transcriptomic profile by ANOVA analysis of the 10 most highly expressed genes
Time frame: Day 2, Day 3 and day 7
the ciliated cell/caliciform ratio
Contact information is provided by the study sponsor or research team.
University Hospital, Montpellier
Other
Acronym: RepCOPDiPS
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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