Abstract

Cellular therapy aims to replace damaged resident cells by restoring cellular and molecular environments suitable for tissue repair and regeneration. Among several candidates, mesenchymal stem/stromal cells (MSCs) represent a critical component of stromal niches known to be involved in tissue homeostasis. In vitro, MSCs appear as fibroblast-like plastic adherent cells regardless of the tissue source. The therapeutic value of MSCs is being explored in several conditions, including immunological, inflammatory and degenerative diseases, as well as cancer. An improved understanding of their origin and function would facilitate their clinical use. The stemness of MSCs is still debated and requires further study. Several terms have been used to designate MSCs, although consensual nomenclature has yet to be determined. The presence of distinct markers may facilitate the identification and isolation of specific subpopulations of MSCs. Regarding their therapeutic properties, the mechanisms underlying their immune and trophic effects imply the secretion of various mediators rather than direct cellular contact. These mediators can be packaged in extracellular vesicles, thus paving the way to exploit therapeutic cell-free products derived from MSCs. Of importance, the function of MSCs and their secretome are significantly sensitive to their environment. Several features, such as culture conditions, delivery method, therapeutic dose and the immunobiology of MSCs, may influence their clinical outcomes. In this review, we will summarize recent findings related to MSC properties. We will also discuss the main preclinical and clinical challenges that may influence the therapeutic value of MSCs and discuss some optimization strategies.

Highlights

  • Mesenchymal stem/stromal cells (MSCs) and their secretome have been investigated for the treatment of several medical indications

  • Establishing a clear definition and characterization of MSCs, identifying the major preclinical and clinical challenges linked to their application and proposing suitable therapeutic optimization strategies may help highlight the value of MSCs and develop stem cell-based therapy

  • The results showed that the expression of CD146 and neuron-glial antigen 2 (NG2) was inversely correlated with doubling time during the serial passage of single-cell-derived human bone marrow (BM)-MSC cultures

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Summary

INTRODUCTION

Mesenchymal stem/stromal cells (MSCs) and their secretome have been investigated for the treatment of several medical indications. Establishing a clear definition and characterization of MSCs (including their origin, terminology and identity), identifying the major preclinical and clinical challenges linked to their application and proposing suitable therapeutic optimization strategies may help highlight the value of MSCs and develop stem cell-based therapy

Definition and Origin
Terminology
PRE-CLINICAL CHALLENGES
Phenotype
Tissue Repair Properties
Aging and Senescence
Culturing and Manufacturing Conditions
Route of Application and Dosing
Hemocompatibility
Complement
Immunogenicity
Patient Health and Immune Status
Clinical Optimization
Findings
CONCLUSION
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