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Multisite studies for optimization of a highly efficient culture assay used for detection of residual undifferentiated human pluripotent stem cells intermingled in cell therapy products. | LitMetric

AI Article Synopsis

  • - MEASURE2 is a Japanese initiative focused on creating standardized testing methods for evaluating tumorigenicity in human pluripotent stem cell-derived cell therapy products.
  • - The project included multisite studies that assessed two key areas: colony formation efficiency of human induced pluripotent stem cells under different conditions and the effectiveness of microbead sorting for enriching hiPSCs.
  • - Findings revealed that a specific culture condition (CEPT) enhanced colony formation and reduced variance across labs compared to a common method, while sorting with anti-Tra-1-60 microbeads showed high efficiency, potentially leading to better tumorigenicity assessments for cell therapy products.

Article Abstract

Introduction: MEASURE2 (Multisite Evaluation Study on Analytical Methods for Non-clinical Safety Assessment of HUman-derived REgenerative Medical Products 2) is a Japanese experimental public-private partnership initiative that aims to standardize testing methods for tumorigenicity evaluation of human pluripotent stem cell (hPSC)-derived cell therapy products (CTPs). MEASURE2 organized multisite studies to optimize the methodology of the highly efficient culture (HEC) assay, a sensitive culture-based assay for detecting residual undifferentiated hPSCs in CTPs.

Methods: In these multisite studies, 1) the efficiency of colony formation by human induced pluripotent stem cells (hiPSCs) under two different culture conditions and 2) the sorting efficiency of microbeads conjugated to various anti-hPSC markers during hiPSC enrichment were evaluated using samples in which hiPSCs were spiked into hiPSC-derived mesenchymal stem cells.

Results: The efficiency of colony formation was significantly higher under culture conditions with the combination of Chroman 1, Emricasan, Polyamines, and Trans-ISRIB (CEPT) than with Y-27632, which is widely used for the survival of hPSCs. Between-laboratory variance was also smaller under the condition with CEPT than with Y-27632. The sorting efficiency of microbeads conjugated with the anti-Tra-1-60 antibody was sufficiently higher (>80%) than those of the other various microbeads investigated.

Conclusions: Results of these multisite studies are expected to contribute to improvements in the sensitivity and robustness of the HEC assay, as well as to the future standardization of the tumorigenicity risk assessment of hPSC-derived CTPs.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11231703PMC
http://dx.doi.org/10.1016/j.reth.2024.06.007DOI Listing

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