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High-Throughput On-Chip Human Mesenchymal Stromal Cell Potency Prediction.

Rebecca S Schneider1,2, Alexandra C Vela2,3, Evelyn Kendall Williams4,5

  • 1School of Chemical and Biomolecular Engineering, Georgia Institute of Technology, Atlanta, GA, 30318, USA.

Advanced Healthcare Materials
|November 2, 2021
PubMed
Summary

A novel microfluidic assay offers a scalable, low-cost method to predict the potency of human mesenchymal stromal cells (hMSCs) for regenerative therapies. This advanced assay improves the prediction of hMSC efficacy, overcoming limitations of current methods.

Keywords:
biomaterialscell therapiesmesenchymal stem/stromal cellsmicrofluidicson-chip technologies

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Area of Science:

  • Biomedical Engineering
  • Cell Therapy
  • Regenerative Medicine

Background:

  • Human mesenchymal stromal cells (hMSCs) show promise for regenerative therapies.
  • Clinical application is hindered by donor variability and inconsistent outcomes.
  • Predicting hMSC potency is crucial for market success but current assays lack scalability and translational power.

Purpose of the Study:

  • To develop a high-throughput, scalable, and cost-effective on-chip microfluidic potency assay for hMSCs.
  • To improve the functional predictive power of hMSC potency assessment.
  • To better recapitulate in vivo secretory responses compared to traditional methods.

Main Methods:

  • Development of an on-chip microfluidic system for hMSC potency assessment.
  • Comparison of hMSC secretory responses in the microfluidic system versus traditional methods.
  • Evaluation of on-chip microfluidic markers against functional immune cell suppression and in vivo models.

Main Results:

  • The microfluidic assay demonstrates improved functional predictive power for hMSC potency.
  • On-chip markers show better correlation with immune cell suppression than traditional markers.
  • hMSC secretory performance in the microfluidic system more closely resembles in vivo conditions.

Conclusions:

  • Current hMSC culture and potency assessment methods have significant limitations.
  • The novel microfluidic system offers enhanced functional predictive power and physiological relevance.
  • This technology could advance the clinical translation of hMSC-based therapies.