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人工树突状细胞:有前景的抗肿瘤免疫治疗新时代

英文原题:Artificial Dendritic Cells: A New Era of Promising Antitumor Immunotherapy.

查看英文原题

Artificial Dendritic Cells: A New Era of Promising Antitumor Immunotherapy.

PubMed 2023/07/19(内容时间) Small Q1 · IF 11.8(JCR 2025)

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中文摘要

近年来抗肿瘤免疫疗法的加速发展使免疫调节成为焦点。这些包括基于树突状细胞(DC)疫苗的免疫治疗,能够引发肿瘤特异性免疫反应并延长生存期。然而,这种个性化治疗存在若干缺点,包括费用高昂、劳动密集且耗时。这激发了人们对生产人工树突状细胞(aDCs)的兴趣,从而开辟了标准化“现成”方案的可能性,并规避繁琐且昂贵的个性化医疗。aDCs利用可针对特定临床应用进行设计和定制的材料。在此,概述了DCs抗原呈递背后的免疫生物学,以试图选择通过aDCs开发需要模拟和/或改进的关键特征。还概述了aDCs的固有特性,这些特性极大地影响其在体内的性能,并因此影响所触发免疫反应的命运。

展开英文摘要原文

The accelerated development of antitumor immunotherapies in recent years has brought immunomodulation into the spotlight. These include immunotherapeutic treatments with dendritic cell (DC)-based vaccines which can elicit tumor-specific immune responses and prolong survival.

However, this personalized treatment has several drawbacks, including being costly, labor-intensive, and time consuming. This has sparked interest in producing artificial dendritic cells (aDCs) to open up the possibility of standardized "off-the-shelf" protocols and circumvent the cumbersome and expensive personalized medicine. aDCs take advantage of materials that can be designed and tailored for specific clinical applications.

Here, an overview of the immunobiology underlying antigen presentation by DCs is provided in an attempt to select the key features to be mimicked and/or improved through the development of aDCs. The inherent properties of aDCs that greatly impact their performance in vivo and, consequently, the fate of the triggered immune response are also outlined.

论文信息

作者
Mateus D、Sebastião AI、Frasco MF、Carrascal MA、Falcão A、Gomes CM、Neves B、Sales MGF
第一作者单位
Faculty of Pharmacy of the University of Coimbra, Coimbra, 3000-548, Portugal.Portugal
通讯作者单位
BioMark@UC/CEB - LABBELS Department of Chemical Engineering, Faculty of Sciences and Technology, University of Coimbra, Coimbra, 3030-790, Portugal.Portugal
文献类型
综述 · 非美国政府资助研究
期刊
Small (Weinheim an der Bergstrasse, Germany)2023 Nov
原文标识
PubMed 37469192 · DOI 10.1002/smll.202303940