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用于癌症免疫治疗的基因工程细胞衍生纳米囊泡。

Genetically engineered cell-derived nanovesicles for cancer immunotherapy.

作者信息

He Shan, Zhao Zongmin

机构信息

Department of Pharmaceutical Sciences, College of Pharmacy, University of Illinois Chicago, Chicago, IL 60612, USA.

Translational Oncology Program, University of Illinois Cancer Center, Chicago, IL 60612, USA.

出版信息

Nanoscale. 2024 May 2;16(17):8317-8334. doi: 10.1039/d3nr06565k.

Abstract

The emergence of immunotherapy has marked a new epoch in cancer treatment, presenting substantial clinical benefits. Extracellular vesicles (EVs), as natural nanocarriers, can deliver biologically active agents in cancer therapy with their inherent biocompatibility and negligible immunogenicity. However, natural EVs have limitations such as inadequate targeting capability, low loading efficacy, and unpredictable side effects. Through progress in genetic engineering, EVs have been modified for enhanced delivery of immunomodulatory agents and antigen presentation with specific cancer targeting ability, deepening the role of EVs in cancer immunotherapy. This review briefly describes typical EV sources, isolation methods, and adjustable targeting of EVs. Furthermore, this review highlights the genetic engineering strategies developed for delivering immunomodulatory agents and antigen presentation in EV-based systems. The prospects and challenges of genetically engineered EVs as cancer immunotherapy in clinical translation are also discussed.

摘要

免疫疗法的出现标志着癌症治疗进入了一个新纪元,带来了显著的临床益处。细胞外囊泡(EVs)作为天然纳米载体,凭借其固有的生物相容性和可忽略不计的免疫原性,能够在癌症治疗中递送生物活性剂。然而,天然EVs存在诸如靶向能力不足、装载效率低和副作用不可预测等局限性。通过基因工程的进展,EVs已被修饰,以增强免疫调节因子的递送和具有特定癌症靶向能力的抗原呈递,从而加深了EVs在癌症免疫治疗中的作用。本综述简要描述了典型的EV来源、分离方法以及EVs的可调节靶向。此外,本综述重点介绍了为在基于EV的系统中递送免疫调节因子和抗原呈递而开发的基因工程策略。还讨论了基因工程EVs作为癌症免疫疗法在临床转化中的前景和挑战。

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