Journal of Translational Medicine (Feb 2023)

Automating iPSC generation to enable autologous photoreceptor cell replacement therapy

  • Laura R. Bohrer,
  • Nicholas E. Stone,
  • Nathaniel K. Mullin,
  • Andrew P. Voigt,
  • Kristin R. Anfinson,
  • Jessica L. Fick,
  • Viviane Luangphakdy,
  • Bradley Hittle,
  • Kimerly Powell,
  • George F. Muschler,
  • Robert F. Mullins,
  • Edwin M. Stone,
  • Budd A. Tucker

DOI
https://doi.org/10.1186/s12967-023-03966-2
Journal volume & issue
Vol. 21, no. 1
pp. 1 – 14

Abstract

Read online

Abstract Background Inherited retinal degeneration is a leading cause of incurable vision loss in the developed world. While autologous iPSC mediated photoreceptor cell replacement is theoretically possible, the lack of commercially available technologies designed to enable high throughput parallel production of patient specific therapeutics has hindered clinical translation. Methods In this study, we describe the use of the Cell X precision robotic cell culture platform to enable parallel production of clinical grade patient specific iPSCs. The Cell X is housed within an ISO Class 5 cGMP compliant closed aseptic isolator (Biospherix XVivo X2), where all procedures from fibroblast culture to iPSC generation, clonal expansion and retinal differentiation were performed. Results Patient iPSCs generated using the Cell X platform were determined to be pluripotent via score card analysis and genetically stable via karyotyping. As determined via immunostaining and confocal microscopy, iPSCs generated using the Cell X platform gave rise to retinal organoids that were indistinguishable from organoids derived from manually generated iPSCs. In addition, at 120 days post-differentiation, single-cell RNA sequencing analysis revealed that cells generated using the Cell X platform were comparable to those generated under manual conditions in a separate laboratory. Conclusion We have successfully developed a robotic iPSC generation platform and standard operating procedures for production of high-quality photoreceptor precursor cells that are compatible with current good manufacturing practices. This system will enable clinical grade production of iPSCs for autologous retinal cell replacement.

Keywords