Cell therapy repairs cornea damage with patient's stem cells gives trial results
medicalxpress.com
medicalxpress.com
From "Sight for sore eyes" (2009) https://newsroom.unsw.edu.au/news/health/sight-sore-eyes :
"A contact lens-based technique for expansion and transplantation of autologous epithelial progenitors for ocular surface reconstruction" (2009) http://dx.doi.org/10.1097/TP.0b013e3181a4bbf2
In this study, they found that only one brand (Bausch and Lomb IIRC) of contact lens worked well as a scaffold for the SC
"Contact lens delivery of stem cells for restoring the ocular surface." (2016) https://scholar.google.com/scholar?hl=en&as_sdt=0%2C33&q=Con...
List of soft contact lens materials: https://en.wikipedia.org/wiki/List_of_soft_contact_lens_mate... ; Hydrogels
So my understanding is that the cornea isn't exactly "alive" anymore. As a guess, you would be better off wondering if there are chemicals getting into the vitreous that cause keratoconus and if those chemicals can in some way be mitigated.
/random internet stranger making conversation. Definitely Not A Doctor.
These are also both fairly good and accessible summaries of very interesting and well-done studies.
I've never browsed medicalxpress.com before but it's 2/2 today, maybe it's just a good aggregator/newsletter we've never head of.
https://www.science.org/doi/10.1126/sciadv.adg6470
> CLET is not available in the United States, as the manufacturing procedure uses xenogeneic murine feeder cells and fetal bovine serum (FBS) and is not compatible with current good manufacturing practices (cGMPs). The use of murine fibroblasts carry a risk of viral contaminants and inflammatory response against murine antigens
> We developed a manufacturing technique to address these shortcomings: cultivated autologous limbal epithelial cells (CALECs). We removed antibiotics and murine feeder cells, used highly reproducible methods for LSC isolation and expansion onto human amniotic membrane, and developed rigorous quality criteria for the manufactured tissue graft.
The article below is by the same author GP linked to and talks about the risks (summary is very low but potentially very serious). The other thing they point out is that the predecessor (CLET) is only available for investigational use whereas CALECs introduced by this paper seem capable of making the leap to commercial use/manufacturing.
Going back to GP's question this does appear to be novel and significantly improved.
https://jamanetwork.com/journals/jamaophthalmology/fullartic...
This modified title needs some fixing
The editors at Science Magazine referred the paper to Science Advances (which generally has a pay-to-publish model).