Wang Jing-Hua, Liu Xiao-Ling, Sun Jian-Mei, Yang Jing-Han, Xu Dong-Hua, Yan Shu-Shan
Clinical Medicine College, Weifang Medical University, Weifang 261000, Shandong Province, China.
Department of Emergency Medicine, Yantai Shan Hospital, Yantai 264001, Shandong Province, China.
World J Stem Cells. 2020 Aug 26;12(8):879-896. doi: 10.4252/wjsc.v12.i8.879.
Mesenchymal stem cells (MSCs) have been reported to possess immune regulatory effects in innate and adaptive immune reactions. MSCs can mediate intercellular communications by releasing extracellular vesicles (EVs), which deliver functional molecules to targeted cells. MSC derived EVs (MSC-EVs) confer altering effects on many immune cells, including T lymphocytes, B lymphocytes, natural killer cells, dendritic cells, and macrophages. A large number of studies have suggested that MSC-EVs participate in regulating autoimmunity related diseases. This characteristic of MSC-EVs makes them be potential biomarkers for the diagnosis and treatment of autoimmunity related diseases.
To verify the potential of MSC-EVs for molecular targeted therapy of autoimmunity related diseases.
Literature search was conducted in PubMed to retrieve the articles published between 2010 and 2020 in the English language. The keywords, such as "MSCs," "EVs," "exosome," "autoimmunity," "tumor immunity," and "transplantation immunity," and Boolean operator "AND" and "NOT" coalesced admirably to be used for searching studies on the specific molecular mechanisms of MSC-EVs in many immune cell types and many autoimmunity related diseases. Studies that did not investigate the molecular mechanisms of MSC-EVs in the occurrence and development of autoimmune diseases were excluded.
A total of 96 articles were chosen for final reference lists. After analyzing those publications, we found that it had been well documented that MSC-EVs have the ability to induce multiple immune cells, like T lymphocytes, B lymphocytes, natural killer cells, dendritic cells, and macrophages, to regulate immune responses in innate immunity and adaptive immunity. Many validated EVs-delivered molecules have been identified as key biomarkers, such as proteins, lipids, and nucleotides. Some EVs-encapsulated functional molecules can serve as promising therapeutic targets particularly for autoimmune disease.
MSC-EVs play an equally important part in the differentiation, activation, and proliferation of immune cells, and they may become potential biomarkers for diagnosis and treatment of autoimmunity related diseases.
据报道,间充质干细胞(MSCs)在先天性和适应性免疫反应中具有免疫调节作用。MSCs可通过释放细胞外囊泡(EVs)介导细胞间通讯,这些细胞外囊泡将功能分子传递给靶细胞。源自MSCs的EVs(MSC-EVs)对许多免疫细胞具有改变作用,包括T淋巴细胞、B淋巴细胞、自然杀伤细胞、树突状细胞和巨噬细胞。大量研究表明,MSC-EVs参与调节自身免疫相关疾病。MSC-EVs的这一特性使其成为自身免疫相关疾病诊断和治疗的潜在生物标志物。
验证MSC-EVs用于自身免疫相关疾病分子靶向治疗的潜力。
在PubMed中进行文献检索,以检索2010年至2020年期间发表的英文文章。“MSCs”“EVs”“外泌体”“自身免疫”“肿瘤免疫”和“移植免疫”等关键词,以及布尔运算符“AND”和“NOT”完美结合,用于搜索关于MSC-EVs在多种免疫细胞类型和多种自身免疫相关疾病中具体分子机制的研究。未研究MSC-EVs在自身免疫性疾病发生和发展中分子机制的研究被排除。
共选择96篇文章作为最终参考文献列表。在分析这些出版物后,我们发现有充分的文献证明,MSC-EVs有能力诱导多种免疫细胞,如T淋巴细胞、B淋巴细胞、自然杀伤细胞、树突状细胞和巨噬细胞,在先天性免疫和适应性免疫中调节免疫反应。许多经过验证的由EVs传递的分子已被确定为关键生物标志物,如蛋白质、脂质和核苷酸。一些包裹在EVs中的功能分子可作为有前景的治疗靶点,特别是对于自身免疫性疾病。
MSC-EVs在免疫细胞的分化、激活和增殖中发挥着同样重要的作用,它们可能成为自身免疫相关疾病诊断和治疗的潜在生物标志物。