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Subretinal transplantation of human embryonic stem cell-derived retinal pigment epithelium (MA09-hRPE): A safety and tolerability evaluation in minipigs. | LitMetric

Subretinal transplantation of human embryonic stem cell-derived retinal pigment epithelium (MA09-hRPE): A safety and tolerability evaluation in minipigs.

Regul Toxicol Pharmacol

Department of Pathology, Asan Medical Institute of Convergence Science and Technology, Asan Medical Center, University of Ulsan College of Medicine, 88, Olympic-ro 43-gil, Songpa-gu, Seoul, Republic of Korea; Department of Pathology, Asan Medical Center, University of Ulsan College of Medicine, 88, Olympic-ro 43-gil, Songpa-gu, Seoul, Republic of Korea. Electronic address:

Published: August 2019

AI Article Synopsis

  • The study assessed the safety and tolerability of higher doses of hESC-derived RPE cells injected subretinally in minipigs, using doses of 60 and 120 × 10 cells/150 μL.
  • Time-course examinations at Weeks 4, 8, and 12 post-surgery indicated gradual changes in retinal blebs and showed cell clusters at the injection site, likely representing an immune response rather than direct evidence of transplanted cells.
  • Overall, the results indicated that the subretinal injections of the higher doses of hESC-derived RPE cells were well-tolerated and deemed safe for the minipigs involved in the study.

Article Abstract

This study aimed to determine the safety and tolerability of the subretinal injection of hESC-derived RPE cells at higher doses than the established clinical dose (5 × 10 cells/150 μL) by using minipigs. The hESC-derived RPE cells (60 or 120 × 10 cells/150 μL) were injected in subretinal region, and minipigs were sacrificed at Weeks 4, 8, and 12 post-surgery. Time-course examination was performed by using fundus photography, optical coherence tomography (OCT), histopathology, and fluorescence in situ hybridization (FISH). After surgery, retinal bleb and pigmentation were seen and retinal bleb became smaller gradually. In histopathology, cell clusters consisting of a uniform population of the round to oval cells were seen at the subretinal injection site. In immunohistochemistry, most of the cells were positive for anti-CD3 and CD45 antibodies but negative for anti-human nuclei antibody; transplanted cells were not detectable by DNA probe in FISH assay. Cell clusters were thought to be a host immune response to trauma or transplanted cells. There were no other changes related to subretinal RPE cell injection. These results suggested that subretinal injection of hESC-derived RPE cells (60 and 120 × 10 cells/150 μL) in minipigs is well-tolerated and safe.

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Source
http://dx.doi.org/10.1016/j.yrtph.2019.04.006DOI Listing

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