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Safety study of allogeneic mesenchymal stem cell therapy in animal model

Intravenous (IV) infusion of mesenchymal stem cells (MSCs) from nascent tissues like Wharton's Jelly of the umbilical cord is reported to offer therapeutic effects against chronic diseases. However, toxicological data essential for the clinical application of these cells are limited. Thus, this...

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Detalles Bibliográficos
Autores principales: Chan, Alvin Man Lung, Ng, Angela Min Hwei, Mohd Yunus, Mohd Heikal, Hj Idrus, Ruszymah Bt, Law, Jia Xian, Yazid, Muhammad Dain, Chin, Kok-Yong, Shamsuddin, Sharen Aini, Mohd Yusof, Mohd Rafizul, Razali, Rabiatul Adawiyah, Mat Afandi, Mohd Asyraf, Hassan, Muhammad Najib Fathi, Ng, See Nguan, Koh, Benson, Lokanathan, Yogeswaran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Japanese Society for Regenerative Medicine 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8861582/
https://www.ncbi.nlm.nih.gov/pubmed/35252487
http://dx.doi.org/10.1016/j.reth.2022.01.008
Descripción
Sumario:Intravenous (IV) infusion of mesenchymal stem cells (MSCs) from nascent tissues like Wharton's Jelly of the umbilical cord is reported to offer therapeutic effects against chronic diseases. However, toxicological data essential for the clinical application of these cells are limited. Thus, this study aimed to determine the safety of IV infusion of Wharton's Jelly derived MSCs (WJ-MSCs) in rats. Fifteen male Sprague–Dawley rats were randomised into the control or treatment group. Each group received an equal volume of saline or WJ-MSC (10 × 10(6) cell/kg) respectively. The animals were evaluated for physical, biochemical and haematological changes at Week 0, 2, 4, 8 and 12 during the 12-week study. Acute toxicity was performed during Week 2 and sub-chronic toxicity during Week 12. At the end of the study, the relative weight of organs was calculated and histology was performed for lung, liver, spleen and kidney. The findings from physical, serum biochemistry and complete blood count demonstrated no statistically significant differences between groups. However, pathological evaluation reported minor inflammation in the lungs for all groups, but visible healing and resolution of inflammation were observed in the treatment group only. Additionally, the histological images of the treatment group had significantly improved pulmonary structures compared to the control group. In summary, the IV administration of WJ-MSC was safe in the rats. Further studies are needed to determine the long-term safety of the WJ-MSC in both healthy and diseased animal models.