Overview
Keratopathy of patients with aniridia leads to epithelial scarring disorders and a progressive clouding of the cornea linked to this abnormal healing (fibrosis). Treatment with autologous serum is usually undertaken to promote epithelial healing.
However, autologous serum does not prevent the formation of fibrosis, whereas growth factor-rich plasma appears to be associated with a reduction in the in vitro expression of fibrosis markers. This study seeks to compare the in vitro healing and anti-fibrotic properties of autologous serum and growth factor rich plasma from aniridia patients and healthy controls.
Description
Blood collection from aniridia patients and healthy controls, half of which will be used to make autologous serum and the other half to make growth factor rich plasma, used for in vitro studies.
A conjunctival impression will also be taken at the inclusion of the patients.
Eligibility
Inclusion Criteria:
For patients with aniridia:
- With aniridia
- Patient weighing more than 43 kg
- If the patient is being treated with autologous serum, a delay of 8 weeks after the last blood collection
- If a blood donation has been made, a delay of 8 weeks must be respected after the last donation
For controls:
- Non-aniridia (no clinical signs)
- Weighing more than 43 kg
- Matched to a case for sex and age +/-10 years
- No known diabetes
- If a blood donation has been made, a delay of 8 weeks must be respected after the latter
Exclusion Criteria:
- Insufficient sample volume
- No conjunctival print
- HBV, HCV, HIV serology positive
- Aniridia not genetically confirmed for cases For each patient excluded, a new patient will be included in order to maintain the number of patients required for data analysis.