4.7 Review

Biodistribution of Mesenchymal Stromal Cells after Administration in Animal Models and Humans: A Systematic Review

Journal

JOURNAL OF CLINICAL MEDICINE
Volume 10, Issue 13, Pages -

Publisher

MDPI
DOI: 10.3390/jcm10132925

Keywords

mesenchymal stromal cell; biodistribution; cell therapy

Funding

  1. Research, Development and Innovation in Biomedicine and Health Sciences in Andalusia [PIGE-0247-2019, PIGE-0242-2019]

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This review focuses on the distribution of mesenchymal stromal cells (MSCs) after injection through different administration routes, including intravenous, intraarterial, intramuscular, intraarticular, and intralesional. The findings suggest that the distribution of MSCs is influenced by the route of administration, with intravenous administration leading to initial lung accumulation and later redistribution, while intraarterial infusion results in widespread distribution throughout the body.
Mesenchymal Stromal Cells (MSCs) are of great interest in cellular therapy. Different routes of administration of MSCs have been described both in pre-clinical and clinical reports. Knowledge about the fate of the administered cells is critical for developing MSC-based therapies. The aim of this review is to describe how MSCs are distributed after injection, using different administration routes in animal models and humans. A literature search was performed in order to consider how MSCs distribute after intravenous, intraarterial, intramuscular, intraarticular and intralesional injection into both animal models and humans. Studies addressing the biodistribution of MSCs in in vivo animal models and humans were included. After the search, 109 articles were included in the review. Intravenous administration of MSCs is widely used; it leads to an initial accumulation of cells in the lungs with later redistribution to the liver, spleen and kidneys. Intraarterial infusion bypasses the lungs, so MSCs distribute widely throughout the rest of the body. Intramuscular, intraarticular and intradermal administration lack systemic biodistribution. Injection into various specific organs is also described. Biodistribution of MSCs in animal models and humans appears to be similar and depends on the route of administration. More studies with standardized protocols of MSC administration could be useful in order to make results homogeneous and more comparable.

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