外泌体临床应用的研究进展

乐佳祺, 徐盛强, 常艳

中国新药杂志 ›› 2026, Vol. 35 ›› Issue (15) : 1605 -1611.

PDF (875KB)
中国新药杂志 ›› 2026, Vol. 35 ›› Issue (15) : 1605 -1611. DOI: 10.20251/j.cnki.1003-3734.2026.15.005
综述

外泌体临床应用的研究进展

    乐佳祺1,2, 徐盛强2, 常艳1,2*
作者信息 +

Research progress of clinical application of exosomes

    LE Jia-qi1,2, XU Sheng-qiang2, CHANG Yan1,2*
Author information +
文章历史 +
PDF (894K)

摘要

外泌体是一种细胞外囊泡,几乎所有类型的细胞都能分泌外泌体,且不同细胞类型来源的外泌体具有不同的特性和生物学功能。越来越多的证据显示外泌体可用于疾病的诊断和治疗,因而备受关注。尽管外泌体的应用潜力巨大,但尚未广泛用于临床,这主要是因其已被中国、美国界定为药物,需要按照更高的稳定性和安全性进行评价。本文对几种不同来源外泌体的功能和临床应用进行了总结,对外泌体相关肿瘤诊断生物标志物进行综述,以期为外泌体的临床应用提供参考。

Abstract

Exosomes are extracellular vesicles that can be secreted by almost all types of cells. They derived from different cell types have different characteristics and biological functions. Accumulating evidence shows that exosomes can be used for the diagnosis and treatment of diseases, and thus they have attracted considerable research interest. Despite their potential, exosomes have not been widely used in clinical practice, mainly because they have been defined as drugs in China and the United States, and are therefore required to be evaluated according to higher standards of stability and safety. This article reviews the functions and clinical applications from several different sources, and tumor-associated diagnostic biomarkers are summarized, to provide a reference for the clinical application of exosomes.

关键词

外泌体 / 临床应用 / 外泌体功能 / 外泌体生物标志物 / 外泌体蛋白质 / 外泌体核酸 / 肿瘤诊断

Key words

exosome / clinical application / exosome function / exosomal biomarkers / exosomal protein / exosomal nucleic acid / tumor diagnosis

引用本文

引用格式 ▾
乐佳祺, 徐盛强, 常艳. 外泌体临床应用的研究进展[J]. 中国新药杂志, 2026, 35(15): 1605-1611 DOI:10.20251/j.cnki.1003-3734.2026.15.005

登录浏览全文

4963

注册一个新账户 忘记密码

参考文献

[1] ZHANG Y, LIU YF, LIU HY, et al. Exosomes: biogenesis, biologic function and clinical potential[J]. Cell Biosci, 2019, 9: 19.
[2] LI MY, LI SS, DU CY, et al. Exosomes from different cells: Characteristics, modifications, and therapeutic applications[J]. Eur J Med Chem, 2020, 207: 112784.
[3] KALLURI R, LEBLEU VS. The biology, function, and biomedical applications of exosomes[J]. Science, 2020, 367(6478): eaau6977.
[4] PENG H, JI WH, ZHAO RC, et al. Exosome: a significant nano-scale drug delivery carrier[J]. J Mater Chem B, 2020, 8(34): 7591-7608.
[5] GURUNG S, PEROCHEAU D, TOURAMANIDOU L, et al. The exosome journey: from biogenesis to uptake and intracellular signalling[J]. Cell Commun Signal, 2021, 19(1): 47.
[6] ABELS ER, BREAKEFIELD XO. Introduction to extracellular vesicles: biogenesis, RNA cargo selection, content, release, and uptake[J]. Cell Mol Neurobiol, 2016, 36(3): 301-312.
[7] TANG YY, ZHOU Y, LI HJ. Advances in mesenchymal stem cell exosomes: a review[J]. Stem Cell Res Ther, 2021, 12(1): 71.
[8] HAN YD, REN J, BAI Y, et al. Exosomes from hypoxia-treated human adipose-derived mesenchymal stem cells enhance angiogenesis through VEGF/VEGF-R[J]. Int J Biochem Cell Biol, 2019, 109: 59-68.
[9] LIU Z, YANG Y, JU JH, et al. miR-100-5p promotes epidermal stem cell proliferation through targeting MTMR3 to activate PIP3/AKT and ERK signaling pathways[J]. Stem Cells Int, 2022, 2022: 1474273.
[10] QIAN XJ, XU C, FANG S, et al. Exosomal microRNAs derived from umbilical mesenchymal stem cells inhibit hepatitis C virus infection[J]. Stem Cells Transl Med, 2016, 5(9): 1190-1203.
[11] ZHOU J, DING YY, ZHANG YQ, et al. Exosomes from bone marrow-derived mesenchymal stem cells facilitate corneal wound healing via regulating the p44/42 MAPK pathway[J]. Graefes Arch Clin Exp Ophthalmol, 2023, 261(3): 723-734.
[12] GAO D, JIANG LL. Exosomes in cancer therapy: a novel experimental strategy[J]. Am J Cancer Res, 2018, 8(11): 2165-2175.
[13] ZHENG L, LI Z, LING W, et al. Exosomes derived from dendritic cells attenuate liver injury by modulating the balance of Treg and Th17 cells after ischemia reperfusion[J]. Cell Physiol Biochem, 2018, 46(2): 740-756.
[14] CHEN R, AI LY, ZHANG JY, et al. Dendritic cell-derived exosomes promote tendon healing and regulate macrophage polarization in preventing tendinopathy[J]. Int J Nanomedicine, 2024, 19: 11701-11718.
[15] KAO CY, PAPOUTSAKIS ET. Extracellular vesicles: exosomes, microparticles, their parts, and their targets to enable their biomanufacturing and clinical applications[J]. Curr Opin Biotechnol, 2019, 60: 89-98.
[16] WANG CX, ZHANG CC, LIU LX, et al. Macrophage-derived mir-155-containing exosomes suppress fibroblast proliferation and promote fibroblast inflammation during cardiac injury[J]. Mol Ther, 2017, 25(1): 192-204.
[17] ZHU ZK, ZHANG XG, LIN XR, et al. Research advances and application progress on miRNAs in exosomes derived from M2 macrophage for tissue injury repairing[J]. Int J Nanomedicine, 2025, 20: 1543-1560.
[18] LIU GZ, CAO RM, LIU QM, et al. M2 macrophages-derived exosomes for osteonecrosis of femoral head treatment: modulating neutrophil extracellular traps formation and endothelial phenotype transition[J]. Bone Res, 2025, 13(1): 42.
[19] RUI SL, DAI LR, ZHANG XS, et al. Exosomal miRNA-26b-5p from PRP suppresses NETs by targeting MMP-8 to promote diabetic wound healing[J]. J Control Release, 2024, 372: 221-233.
[20] ZHAO YH, DU L, HAN L, et al. Exosomal hsa_circ_0093884 derived from endothelial progenitor cells promotes therapeutic neovascularization via miR-145/SIRT1 pathway[J]. Biomed Pharmacother, 2024, 173: 116343.
[21] YUAN FF, PENG W, YANG YY, et al. Endothelial progenitor cell-derived exosomes promote anti-inflammatory macrophages via SOCS3/JAK2/STAT3 axis and improve the outcome of spinal cord injury[J]. J Neuroinflammation, 2023, 20(1): 156.
[22] KIM HI, PARK J, ZHU Y, et al. Recent advances in extracellular vesicles for therapeutic cargo delivery[J]. Exp Mol Med, 2024, 56(4): 836-849.
[23] DEVARAJ E, PERUMAL E, SUBRAMANIYAN R, et al. Liver fibrosis: Extracellular vesicles mediated intercellular communication in perisinusoidal space[J]. Hepatology, 2022, 76(1): 275-285.
[24] KIM J, LEE CB, SHIN Y, et al. sEVs from tonsil-derived mesenchymal stromal cells alleviate activation of hepatic stellate cells and liver fibrosis through miR-486-5p[J]. Mol Ther, 2021, 29(4): 1471-1486.
[25] LIN Y, YAN MC, BAI ZT, et al. Huc-MSC-derived exosomes modified with the targeting peptide of aHSCs for liver fibrosis therapy[J]. J Nanobiotechnology, 2022, 20(1): 432.
[26] YUAN DF, ZHAO YL, BANKS WA, et al. Macrophage exosomes as natural nanocarriers for protein delivery to inflamed brain[J]. Biomaterials, 2017, 142: 1-12.
[27] HANEY MJ, KLYACHKO NL, ZHAO YL, et al. Exosomes as drug delivery vehicles for Parkinson's disease therapy[J]. J Control Release, 2015, 207: 18-30.
[28] MEISSNER WG, FRASIER M, GASSER T, et al. Priorities in Parkinson's disease research[J]. Nat Rev Drug Discov, 2011, 10(5): 377-393.
[29] VOLPICELLI-DALEY LA, LUK KC, PATEL TP, et al. Exogenous α-synuclein fibrils induce Lewy body pathology leading to synaptic dysfunction and neuron death[J]. Neuron, 2011, 72(1): 57-71.
[30] YANG JL, LUO SL, ZHANG JC, et al. Exosome-mediated delivery of antisense oligonucleotides targeting α-synuclein ameliorates the pathology in a mouse model of Parkinson's disease[J]. Neurobiol Dis, 2021, 148: 105218.
[31] ESTEVES M, ABREU R, FERNANDES H, et al. microRNA-124-3p-enriched small extracellular vesicles as a therapeutic approach for Parkinson's disease[J]. Mol Ther, 2022, 30(10): 3176-3192.
[32] SALARPOUR S, FOROOTANFAR H, POURNAMDARI M, et al. Paclitaxel incorporated exosomes derived from glioblastoma cells: comparative study of two loading techniques[J]. Daru, 2019, 27(2): 533-539.
[33] HU CM, JIANG W, LV MJ, et al. Potentiality of exosomal proteins as novel cancer biomarkers for liquid biopsy[J]. Front Immunol, 2022, 13: 792046.
[34] MELO SA, LUECKE LB, KAHLERT C, et al. Glypican-1 identifies cancer exosomes and detects early pancreatic cancer[J]. Nature, 2015, 523(7559): 177-182.
[35] SKOG J, WÜRDINGER T, VAN RIJN S, et al. Glioblastoma microvesicles transport RNA and proteins that promote tumour growth and provide diagnostic biomarkers[J]. Nat Cell Biol, 2008, 10(12): 1470-1476.
[36] WAHID F, SHEHZAD A, KHAN T, et al. microRNAs: synthesis, mechanism, function, and recent clinical trials[J]. Biochim Biophys Acta, 2010, 1803(11): 1231-1243.
[37] LI CY, ZHOU T, CHEN J, et al. The role of Exosomal miRNAs in cancer[J]. J Transl Med, 2022, 20(1): 6.
[38] LI QR, TIAN J, CHEN CQ, et al. Meta-analysis of the diagnostic value of exosomal microRNAs in renal cell carcinoma[J]. Front Oncol, 2024, 14: 1441429.
[39] GUO XL, GAO L, WANG Y, et al. Advances in long noncoding RNAs: identification, structure prediction and function annotation[J]. Brief Funct Genomics, 2016, 15(1): 38-46.
[40] SONG XD, DUAN LL, DONG YS. Diagnostic accuracy of exosomal long noncoding RNAs in diagnosis of NSCLC: a meta-analysis[J]. Mol Diagn Ther, 2024, 28(4): 455-468.
[41] ZHANG F, JIANG JJ, QIAN H, et al. Exosomal circRNA: emerging insights into cancer progression and clinical application potential[J]. J Hematol Oncol, 2023, 16(1): 67.
[42] CAO YX, LIU XB, LIU JY, et al. Diagnostic value of exosomal noncoding RNA in lung cancer: a meta-analysis[J]. Front Oncol, 2024, 14: 1357248.
[43] XU GL, JIN J, FU ZH, et al. Extracellular vesicle-based drug overview: research landscape, quality control and nonclinical evaluation strategies[J]. Signal Transduct Target Ther, 2025, 10(1): 255.
[44] MOREL O, MOREL N, FREYSSINET JM, et al. Platelet microparticles and vascular cells interactions: a checkpoint between the haemostatic and thrombotic responses[J]. Platelets, 2008, 19(1): 9-23.
[45] HUNT CJ. Technical considerations in the freezing, low-temperature storage and thawing of stem cells for cellular therapies[J]. Transfus Med Hemother, 2019, 46(3): 134-150.
[46] AHMADIAN S, JAFARI N, TAMADON A, et al. Different storage and freezing protocols for extracellular vesicles: a systematic review[J]. Stem Cell Res Ther, 2024, 15(1): 453.

基金资助

国家发改委支持先进制造业和现代服务业发展专项资助项目

AI Summary AI Mindmap
PDF (875KB)

6

访问

0

被引

详细

导航
相关文章

AI思维导图

/