Pathogen-free, plasma-poor platelet lysate and expansion of human mesenchymal stem cells

Paola Iudicone, Daniela Fioravanti, Giuseppina Bonanno

  • 1Immunohematology and Transfusion Medicine, San Camillo Forlanini Hospital, Rome, Italy. lpierelli@me.com.

Abstract

Insights

Pathogen-inactivated platelet lysate (PI-PL) effectively supports mesenchymal stem cell (MSC) expansion, matching traditional supplements. This human-derived product offers a safe and standardized alternative for clinical-grade MSC cultures.

Area of Science:

  • Cell Biology
  • Biotechnology
  • Regenerative Medicine

Background:

  • Mesenchymal stem cells (MSC) require specialized supplements for clinical-grade expansion.
  • Platelet lysate (PL) is a promising human-derived supplement rich in growth factors, potentially replacing animal serum.
  • Standardized and safe human supplements are crucial for ex vivo MSC production.

Purpose of the Study:

  • To develop and evaluate a plasma-poor, pathogen-inactivated platelet lysate (PI-PL) as a supplement for clinical-grade MSC expansion.
  • To compare the efficacy of PI-PL with traditional supplements like fetal bovine serum (FBS) and non-inactivated PL.
  • To assess the impact of pathogen inactivation on growth factor concentration and MSC growth-supporting capacity.

Main Methods:

  • Production of PI-PL by pooling platelet units, pathogen inactivation, and freezing/thawing cycles.
  • Comparison of PI-PL and control PL lots for MSC selection and expansion from bone marrow.
  • Evaluation of PI-PL's impact on growth factor concentration and MSC growth.
  • Assessment of MSC immunoregulatory properties in vitro using mixed lymphocyte culture (MLC) and peripheral blood mononuclear cell (PBMC) proliferation assays.

Main Results:

  • PI-PL and control PL exhibited comparable concentrations of key growth factors essential for MSC stimulation.
  • Both PI-PL and control PL supported similar MSC growth and expansion, including for frozen/thawed cells.
  • Pathogen inactivation did not significantly alter growth factor levels or MSC growth support.
  • PI-PL-derived MSC maintained multilineage differentiation potential and immunoregulatory functions.
  • Fetal bovine serum (FBS) demonstrated significantly lower efficacy in supporting MSC expansion compared to PL and PI-PL.

Conclusions:

  • Pathogen-inactivated platelet lysate (PI-PL) is a standardized, plasma-poor, human-derived supplement suitable for clinical-grade MSC expansion.
  • PI-PL offers a safe and effective alternative to animal-derived supplements in ex vivo cell culture.
  • This human supplement supports MSC growth, differentiation, and immunomodulatory functions, crucial for therapeutic applications.

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