Implementation of a Protocol for the Transdifferentiation of Buccal Mucosal Epithelium Into Corneal Epithelium
TransBuCor
1 other identifier
interventional
4
1 country
1
Brief Summary
Objectives The transparent surface of the eye, called the cornea, plays a crucial role in transmitting light to the retina and in protecting the eye. On its external surface, the cornea is composed of a constantly renewing multistratified epithelium. This mechanism is fueled by stem cells located in the limbus (the transition zone between the cornea and the sclera). Limbal Stem Cell Deficiency (LSCD) is characterized by a decrease or cessation of epithelial renewal and neovascularization of the cornea. Consequently, the cornea loses its integrity and transparency. This visually impairing condition is currently in a therapeutic impasse as only autologous limbal or allogeneic corneal grafts are viable options, but they pose significant risks to patients. Studies have shown that the oral cavity contains stem cells that can be isolated, cultured, and transdifferentiated into limbal stem cells (LSCs). However, to date, these studies are limited, and no protocol has been validated. In this study, the advantage of the accessibility of the oral cavity is used to develop a protocol for differentiating cells from the oral mucosa into limbal stem cells (LSCs) for use in a future clinical trial with patients. Methodology This prospective monocentric study will be conducted on patients from the ophthalmology department of the Montpellier University Hospital who have an indication for conjunctival reconstruction. After obtaining consent from the patients, cells from the oral wall will be sent to the tissue bank of the Montpellier University Hospital, where they will be cultured. Finally, the transdifferentiation steps will be analyzed by the "Eye" research team at the Institute of Neuroscience in Montpellier, which is collaborating on the project. The investigators have established objective factors to assess the success of the developed protocol based on the literature : (i) \> 3% of stem cells in primary cultures, (ii) \<10% aborted colonies, (iii) Expression of LSC markers (Pax6, Krt14, p63).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Jun 2024
1 active site
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Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
January 24, 2024
CompletedFirst Posted
Study publicly available on registry
February 20, 2024
CompletedStudy Start
First participant enrolled
June 19, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
June 1, 2025
CompletedAugust 19, 2024
August 1, 2024
12 months
January 24, 2024
August 16, 2024
Conditions
Keywords
Outcome Measures
Primary Outcomes (5)
Successful Transdifferentiation
Successful differentiation, defined by the percentage of stem cells on primary cultures ≥ 3%
change over time between Baseline and 14 days
Successful Transdifferentiation
Successful differentiation, defined by the percentage of aborted colonies \< 10%.
change over time between Baseline and 14 days
Successful Transdifferentiation
The quantitative real-time polymerase chain reaction, (qPCR) technique will be used to monitor expression levels of limbal stem cell markers such as Krt14 and Krt5. The qPCR technique will be used to monitor expression levels of transcription factors.
change over time between Baseline and 14 days
Successful Transdifferentiation
Successful differentiation, defined by the presence of transcription factors p63 and Pax6 The qPCR technique will be used to monitor expression levels of transcription factors.
change over time between Baseline and 14 days
Successful Transdifferentiation
The qPCR technique will be used wiil be used to monitor the absence of expression of markers of terminal differentiation of corneal epithelial cells, such as Krt3 and Krt12
change over time between Baseline and 14 days
Study Arms (1)
Reconstruction conjonctival
EXPERIMENTALPatients undergoing conjunctival reconstruction using oral mucosa
Interventions
Conjunctival reconstruction using buccal mucosa taken from the patient's mouth. Following the reconstruction operation, an additional biopsy of buccal mucosa will be taken to develop a laboratory protocol for the transdifferentiation of these buccal cells into corneal epithelial stem cells.
Eligibility Criteria
You may qualify if:
- Presenting an indication for conjunctival reconstruction using oral mucosa (for example because of a recurrent pterygium, conjunctival carcinoma or ocular burn)
- Written consent to participate in this research
You may not qualify if:
- Chronic infection (HIV, hepatitis, tuberculosis, Lyme disease)
- Oral pathology which could affect the health of the oral mucosa tissue according to the opinion of the investigating doctor
- Uncontrolled systemic disease
- Pregnant or breastfeeding
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
CHU Gui de Chauliac - Service d'Ophtamologie
Montpellier, Occitanie, 34295, France
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Vincent Daien, MD PhD
v-daien@chu-montpellier.fr
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 24, 2024
First Posted
February 20, 2024
Study Start
June 19, 2024
Primary Completion
June 1, 2025
Study Completion
June 1, 2025
Last Updated
August 19, 2024
Record last verified: 2024-08
Data Sharing
- IPD Sharing
- Will not share