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Limited Potential or Unfavorable Manipulations? Strategies Toward Efficient Mesenchymal Stem/Stromal Cell
Antonina Lavrentieva1, Andrea Hoffmann2, Cornelia Lee-Thedieck3
1Institute of Technical Chemistry, Leibniz University Hannover, Hanover, Germany.
Abstract:
Despite almost 50 years of research and over 20 years of preclinical and clinical studies, the question of curative potential of mesenchymal stem/stromal cells (MSCs) is still widely discussed in the scientific community. Non-reproducible treatment outcomes or even absence of treatment effects in comparison to control groups challenges the potential of these cells for routine application both in tissue engineering and in regenerative medicine. One of the reasons of such outcomes is non-standardized and often disadvantageous ex vivo manipulation of MSCs prior therapy. In most cases, clinically relevant cell numbers for MSC-based therapies can be only obtained by in vitro expansion of isolated cells. In this mini review, we will discuss point by point possible pitfalls in the production of human MSCs for cell therapies, without consideration of material-based applications. Starting with cell source, choice of donor and recipient, as well as isolation methods, we will then discuss existing expansion protocols (two-/three-dimensional cultivation, basal medium, medium supplements, static/dynamic conditions, and hypoxic/normoxic conditions) and influence of these strategies on the cell functionality after implantation. The role of potency assays will also be addressed. The final aim of this mini review is to illustrate the heterogeneity of current strategies for gaining MSCs for clinical applications with their strengths and weaknesses. Only a careful consideration and standardization of all pretreatment processes/methods for the different applications of MSCs will ensure robust and reproducible performance of these cell populations in the different experimental and clinical settings.
Insights
Standardizing mesenchymal stem/stromal cell (MSC) production is crucial for effective cell therapies. Addressing pitfalls in MSC isolation and expansion ensures reproducible outcomes in regenerative medicine and tissue engineering.
Area of Science:
- Cell Biology
- Regenerative Medicine
- Biotechnology
Background:
- Mesenchymal stem/stromal cells (MSCs) show therapeutic promise but face challenges in reproducibility.
- Non-standardized ex vivo manipulation and in vitro expansion hinder clinical application of MSCs.
- Varied treatment outcomes necessitate a closer look at MSC production for cell therapies.
Purpose of the Study:
- To review critical pitfalls in human MSC production for cell therapies.
- To analyze the impact of different production strategies on MSC functionality.
- To highlight the heterogeneity in current MSC gain strategies and their implications.
Main Methods:
- Review of cell source, donor/recipient selection, and isolation methods for MSCs.
- Analysis of various in vitro expansion protocols: 2D/3D cultivation, media, supplements, static/dynamic, hypoxic/normoxic conditions.
- Discussion on the role and limitations of potency assays in MSC production.
Main Results:
- Identified numerous potential pitfalls in MSC production, from donor selection to expansion conditions.
- Demonstrated how diverse expansion strategies significantly influence MSC functionality post-implantation.
- Highlighted the heterogeneity of current MSC production methods, impacting clinical translation.
Conclusions:
- Standardization of MSC pretreatment processes is essential for robust and reproducible cell therapies.
- Careful consideration of all production steps is required to ensure consistent MSC performance.
- Addressing these production variables will advance the clinical use of MSCs in regenerative medicine.
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