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Long-term survival in non-human primates of stem cell-derived, MHC-unmatched corneal epithelial cell sheets

When corneal epithelial stem cells residing in the corneal limbus become dysfunctional, called a limbal stem cell deficiency (LSCD), corneal transparency is decreased, causing severe vision loss. Transplantation of corneal epithelial cell sheets (CEPS) derived from stem cells, including induced plur...

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Detalles Bibliográficos
Autores principales: Yoshinaga, Yu, Soma, Takeshi, Azuma, Shohei, Maruyama, Kazuichi, Hashikawa, Yoshiko, Katayama, Tomohiko, Sasamoto, Yuzuru, Takayanagi, Hiroshi, Hosen, Naoki, Shiina, Takashi, Ogasawara, Kazumasa, Hayashi, Ryuhei, Nishida, Kohji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9287743/
https://www.ncbi.nlm.nih.gov/pubmed/35750044
http://dx.doi.org/10.1016/j.stemcr.2022.05.018
Descripción
Sumario:When corneal epithelial stem cells residing in the corneal limbus become dysfunctional, called a limbal stem cell deficiency (LSCD), corneal transparency is decreased, causing severe vision loss. Transplantation of corneal epithelial cell sheets (CEPS) derived from stem cells, including induced pluripotent stem cells, is a promising treatment for LSCD. However, the potential effect of human leukocyte antigen (HLA) concordance on CEPS transplantation has not been addressed. Here, we show that there is no difference in the immune response to CEPS between HLA-matched and -unmatched peripheral blood mononuclear cells in mixed lymphocyte reactions. CEPS transplantation in cynomolgus monkeys revealed that the immune response to major histocompatibility-unmatched CEPS was not strong and could be controlled by local steroid administration. Furthermore, programmed death ligand 1 was identified as an immunosuppressive molecule in CEPS under inflammatory conditions in vitro. Our results indicate that corneal epithelium has low immunogenicity and allogeneic CEPS transplantation requires mild immunosuppression.