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人脐带间充质干细胞来源外泌体的非临床安全性评价。

Non-Clinical Safety Evaluation of Exosomes Derived from Human Umbilical Cord Mesenchymal Stem Cells in Cynomolgus Monkeys.

机构信息

Medical College, Guangxi University, Nanning, Guangxi Zhuang Autonomous Region, People's Republic of China.

Department of Research and Development, Guangxi Taimei Rensheng Biotechnology Co., Ltd, Nanning, Guangxi Zhuang Autonomous Region, People's Republic of China.

出版信息

Int J Nanomedicine. 2024 May 27;19:4923-4939. doi: 10.2147/IJN.S454438. eCollection 2024.

Abstract

PURPOSE

In recent years, exosomes have been proved to be used to treat many diseases. However, due to the lack of uniform quality control standards for exosomes, the safety of exosomes is still a problem to be solved, especially now more and more exosomes are used in clinical trials, and its non-clinical safety evaluation is particularly important. However, there is no safety evaluation standard for exosomes at present. Therefore, this study will refer to the evaluation criteria of therapeutic biological products, adopt non-human primates to evaluate the non-clinical safety of human umbilical cord mesenchymal stem cell exosomes from the general pharmacology and immunotoxicity, aiming at establishing a safety evaluation system of exosomes and providing reference for the clinical application of exosomes in the future.

METHODS

3.85 × 10 exosomes derived from human umbilical cord mesenchymal stem cells were injected into cynomolgus monkeys intravenously. The changes of general clinical conditions, hematology, immunoglobulin, Th1/Th2 cytokines, T lymphocytes and B lymphocytes, and immune organs were observed before and within 14 days after injection.

RESULTS

The results showed that exosomes did not have obvious pathological effects on the general clinical conditions, blood, coagulation function, organ coefficient, immunoglobulin, Th1/Th2 cytokines, lymphocytes, major organs, and major immune organs (spleen, thymus, bone marrow) of cynomolgus monkeys. However, the number of granulocyte-macrophage colonies in exosomes group was significantly higher than that in control group.

CONCLUSION

To sum up, the general pharmacological results and immunotoxicity results showed that the injection of 3.85 × 10 exosomes may have no obvious adverse reactions to cynomolgus monkeys. This dose of exosomes is relatively safe for treatment, which provides basis research for non-clinical safety evaluation of exosomes and provides reliable research basis for future clinical application of exosomes.

摘要

目的

近年来,外泌体已被证明可用于治疗多种疾病。然而,由于缺乏对外泌体的统一质量控制标准,外泌体的安全性仍是一个待解决的问题,尤其是现在越来越多的外泌体应用于临床试验,其非临床安全性评价尤为重要。然而,目前尚无外泌体的安全性评价标准。因此,本研究将参考治疗性生物制品的评价标准,采用食蟹猴从一般药理学和免疫毒性方面评价人脐带间充质干细胞来源外泌体的非临床安全性,旨在建立外泌体的安全性评价体系,为外泌体未来的临床应用提供参考。

方法

将 3.85×10exosomes 静脉注射入食蟹猴体内。观察注射前后 14 天内食蟹猴一般临床状况、血常规、免疫球蛋白、Th1/Th2 细胞因子、T 淋巴细胞和 B 淋巴细胞及免疫器官的变化。

结果

结果显示,外泌体对食蟹猴的一般临床状况、血液、凝血功能、脏器系数、免疫球蛋白、Th1/Th2 细胞因子、淋巴细胞、主要脏器和主要免疫器官(脾、胸腺、骨髓)无明显的病理作用。但外泌体组粒-巨噬细胞集落数明显高于对照组。

结论

综上所述,一般药理学结果和免疫毒性结果表明,注射 3.85×10exosomes 可能对食蟹猴没有明显的不良反应。该剂量的外泌体治疗相对安全,为外泌体的非临床安全性评价提供了基础研究,为外泌体的未来临床应用提供了可靠的研究依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/691f/11143447/ed27b7e5dc21/IJN-19-4923-g0001.jpg

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