Adipose-derived mesenchymal stromal cells: A study on safety and efficacy in ocular inflammation

Ocul Surf. 2024 Oct:34:523-534. doi: 10.1016/j.jtos.2024.11.001. Epub 2024 Nov 13.

Abstract

Purpose: This study explores the application of adipose-derived mesenchymal stromal cells (adMSCs) as a therapy for ocular inflammatory diseases utilizing a chronic GVHD model.

Methods: Human adMSCs were administered via subconjunctival injection into mice with chronic ocular GVHD. Clinical scores and changes in T cell populations were analyzed.

Results: The study showed significant improvement in corneal integrity, including epithelial damage, opacity, thickness, and structure, after subconjunctival adMSC transplantation. Additionally, adMSC transplantation increased CD45+ and Foxp3+ Tregs while decreasing CD4+ T cells, 1IL17A+ Th17 cells, and IFNγ+ Th1 cells in local cervical lymph nodes. Moreover, adMSC-conditioned media enhanced wound closure and cell migration toward the wound bed in vitro. The cells disappeared within a week suggesting that trophic factors were involved.

Conclusion: The dual benefit of adMSCs in immune-related ocular disorders underscores their potential for clinical application. This study focuses on subconjunctival delivery, effects of adMSCs and migration post-injection, with implications for optimizing cellular therapy application. The observed dual action, combining immunomodulation and tissue repair enhancement, underscores holistic approach of adMSC therapy in regenerative medicine, making it a potent treatment for diseases involving inflammation and tissue damage in the ocular surface.

Keywords: Adipose-derived stromal cells; Graft-versus-host disease (GVHD); Immunomodulation; Inflammation; Mesenchymal stem cells (MSCs).

MeSH terms

  • Adipose Tissue / cytology
  • Animals
  • Cells, Cultured
  • Conjunctiva / pathology
  • Disease Models, Animal*
  • Female
  • Graft vs Host Disease / therapy
  • Humans
  • Mesenchymal Stem Cell Transplantation* / methods
  • Mesenchymal Stem Cells* / cytology
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL