4.1 Article

hUC-MSCs: evaluation of acute and long-term routine toxicity testing in mice and rats

期刊

CYTOTECHNOLOGY
卷 74, 期 1, 页码 17-29

出版社

SPRINGER
DOI: 10.1007/s10616-021-00502-2

关键词

Acute toxicity; Biotransformation and toxicokinetics; Human umbilical cord-derived mesenchymal stem cells; Long-term toxicity; Safety evaluation

资金

  1. National natural science foundation of China [81860089]
  2. Doctoral Foundation of Guizhou Medical University [[2020]018]
  3. Non-profit Central Research Institute Fund of Chinese Academy of Medical Sciences [2018PT31048]
  4. Science and Technology Foundation Project of Guizhou Health Committee [gzwjkj2019-1-099]

向作者/读者索取更多资源

This study evaluated the acute and long-term toxicity of human umbilical cord-derived mesenchymal stem cells (hUC-MSCs) in mice and rats. The results showed that there was no obvious acute toxicity of hUC-MSCs in mice at the maximum tolerated dose. Long-term toxicity tests in rats also didn't show significant differences between HUC-MSC-treated and control groups.
Human umbilical cord-derived mesenchymal stem cells (hUC-MSCs) are present in human umbilical connective tissue and can differentiate into various cell types. Our previous studies have proved that hUC-MSCs do not lead to allergies and tumorigenesis. In the present study, the acute and long-term toxicity of hUC-MSCs in mice and rats was evaluated. The acute toxicity of hUC-MSCs was assessed in 8-week-old mice receiving two caudal intravenous (i.v.) injections of hUC-MSCs at the maximum tolerated dose of 1.5 x 10(7) cells/kg with an interval of 8 h and the observation period sustained for 14 days. For the long-term toxicity evaluation, rats were randomly divided into control, low-dose (3.0 x 10(5) cells/kg), mid-dose (1.5 x 10(6) cells/kg), and high-dose (7.5 x 10(6) cells/kg) groups, which were treated with hUC-MSCs via a caudal i.v. injection every 3 days for 90 days. Weight and food intake evaluation was performed for all rats for 2 weeks after the hUC-MSC administration. The animals were then sacrificed for hematological, blood biochemical, and pathological analyses, as well as organ index determination. We observed no obvious acute toxicity of hUC-MSCs in mice at the maximum tolerated dose. Long-term toxicity tests in rats showed no significant differences between HUC-MSC-treated and control groups in the following parameters: body weight, hematological and blood biochemical parameters, and histopathologic changes in the heart, liver, kidneys, and lungs. This study provides evidence of the safety of i.v. hUC-MSCs infusion for future clinical therapies.

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