4.4 Review

In situ Tissue Regeneration in the Cornea from Bench to Bedside

Journal

CELLS TISSUES ORGANS
Volume 211, Issue 4, Pages 506-526

Publisher

KARGER
DOI: 10.1159/000514690

Keywords

Exosomes; Regulatory considerations; Cornea; Transplantation; Biomaterials; Regeneration; Clinical trial

Funding

  1. CIHR Canada
  2. NSERC Canada
  3. Canadian Stem Cell Network
  4. Swedish Research Council
  5. VINNOVA Sweden
  6. Euronanomed 2
  7. Euronanomed 3
  8. Fonds de la recherche en sante du Quebec (FRQS)
  9. Tier 1 Canada Research Chair for Biomaterials and Stem Cells in Ophthalmology
  10. Caroline Durand Foundation Research Chair for Cellular Therapy in the Eye
  11. Natural Sciences and Engineering Research Council of Canada (NSERC)

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Corneal blindness is the fourth leading cause of global blindness, with over 90% of cases occurring in low- and middle-income regions. While corneal transplantation is effective, the shortage of corneal graft tissue in many LMIRs limits access to this treatment option. Various biomaterial approaches, including in situ tissue regeneration, show promise for treating corneal injuries and diseases, potentially offering alternatives to organ transplantation and improving patient outcomes.
Corneal blindness accounts for 5.1% of visual deficiency and is the fourth leading cause of blindness globally. An additional 1.5-2 million people develop corneal blindness each year, including many children born with or who later develop corneal infections. Over 90% of corneal blind people globally live in low- and middle-income regions (LMIRs), where corneal ulcers are approximately 10-fold higher compared to high-income countries. While corneal transplantation is an effective option for patients in high-income countries, there is a considerable global shortage of corneal graft tissue and limited corneal transplant programs in many LMIRs. In situ tissue regeneration aims to restore diseases or damaged tissues by inducing organ regeneration. This can be achieved in the cornea using biomaterials based on extracellular matrix (ECM) components like collagen, hyaluronic acid, and silk. Solid corneal implants based on recombinant human collagen type III were successfully implanted into patients resulting in regeneration of the corneal epithelium, stroma, and sub-basal nerve plexus. As ECM crosslinking and manufacturing methods improve, the focus of biomaterial development has shifted to injectable, in situ gelling formulations. Collagen, collagen-mimetic, and gelatin-based in situ gelling formulas have shown the ability to repair corneal wounds, surgical incisions, and perforations in in-vivo models. Biomaterial approaches may not be sufficient to treat inflammatory conditions, so other cell-free therapies such as treatment with tolerogenic exosomes and extracellular vesicles may improve treatment outcomes. Overall, many of the technologies described here show promise as future medical devices or combination products with cell or drug-based therapies. In situ tissue regeneration, particularly with liquid formulas, offers the ability to triage and treat corneal injuries and disease with a single regenerative solution, providing alternatives to organ transplantation and improving patient outcomes.

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