Translation of a human induced pluripotent stem cell-derived ovarian support cell product to a Phase 3 enabling clinical grade product for in vitro fertilization treatment
Paulsen, B.; Barrachina, F.; Piechota, S.; Noblett, A. D.; Johnson, M.; Kats, S.; Lew, C.; Marchante, M.; Figueroa, A. B.; Garcia Granada, I.; Ingalls Lopez, E.; Martinez Martinez, E.; Ricra, P.; Carlos, C.; Meza, J.; Montanchez, W.; Pino, P.; Reategui, C.; Noriega, E.; Elias, A.; Noriega-Portella, L.; Haddad, G.; Radenkovic, D.; Moran, E.; Villanueva, P.; Guiterrez, J.; Guzman, L.; Bortolleto, P.; Albertini, D. F.; De Vos, M.; Kramme, C. C.
Show abstract
Human induced pluripotent stem cells (hiPSCs) show great promise in the development of novel strategies to mitigate reproductive diseases and promote successful reproductive outcomes. Recently, a novel approach for the fast and efficient differentiation of ovarian support cells (OSCs) to generate a versatile platform for basic research and clinical applications was demonstrated. This study details the clinical process development and application of an OSC product, known as Fertilo, to improve the in vitro maturation (IVM) of human oocytes, a method referred to as OSC-IVM. First, transcription factor (TF) mediated OSC differentiation using research-grade raw materials was shown to produce granulosa-like cells that improve the MII maturation rate of human oocytes. To support clinical application, several raw material upgrades were initiated, including substitution of the differentiation matrix with a higher-quality alternative, laminin-521, and the generation of a clinically suitable hiPSC seed bank and master cell bank. Single cell RNA sequencing of OSCs generated using the updated protocol for clinical translation demonstrated the consistency and reproducibility of cellular outcomes. Next, analytical release testing of the clinical product was performed and a murine oocyte maturation assay was developed to establish the potency of OSCs for use in OSC-IVM. Finally, the qualified Fertilo product was applied in a two-phase longitudinal cohort analysis, with the results showing improvement in key outcomes compared to traditional IVM treatment. Our findings demonstrate the first-time clinical development and application of an hiPSC-derived product to improve reproductive outcomes after IVM and advance womens health.
Matching journals
The top 6 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- Application of machine learning to discriminate photoreceptor cell species in xenotransplanted chimeric retinas 87%
- Fetal spina bifida associates with dysregulation in nutrient-sensitive placental gene networks: findings from a matched case-control study 87%
- A randomized, controlled, feasibility study of RD-X19 in patients with mild-to-moderate COVID-19 in the outpatient setting 86%
Similar papers in this journal
Similar papers in this journal
- Establishment and functional characterization of bovine endometrial epithelial organoids 93%
- Biosensor capability of the endometrium is mediated in part, by altered miRNA cargo from conceptus-derived extracellular vesicles. 92%
- Platelets as key cells in endometriosis patients: insights from small extracellular vesicles in peritoneal fluid and endometriotic lesions analysis 91%
Similar papers in this journal
Similar papers in this journal
- Novel therapeutic strategies for injured endometrium: Autologous intrauterine transplantation of menstrual blood-derived cells from infertile patients 94%
- Culture of pluripotent stem cells in microscale droplets modulates differentiation and tissue patterning towards organoids on chip 92%
- Engineering a Controlled Cardiac Multilineage Co-Differentiation Process Using Statistical Design of Experiments 92%
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.