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用于产生治疗性免疫反应的生物材料策略。

Biomaterial strategies for generating therapeutic immune responses.

作者信息

Kelly Sean H, Shores Lucas S, Votaw Nicole L, Collier Joel H

机构信息

Duke University, Department of Biomedical Engineering, United States.

Duke University, Department of Biomedical Engineering, United States.

出版信息

Adv Drug Deliv Rev. 2017 May 15;114:3-18. doi: 10.1016/j.addr.2017.04.009. Epub 2017 Apr 25.

DOI:10.1016/j.addr.2017.04.009
PMID:28455189
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5606982/
Abstract

Biomaterials employed to raise therapeutic immune responses have become a complex and active field. Historically, vaccines have been developed primarily to fight infectious diseases, but recent years have seen the development of immunologically active biomaterials towards an expanding list of non-infectious diseases and conditions including inflammation, autoimmunity, wounds, cancer, and others. This review structures its discussion of these approaches around a progression from single-target strategies to those that engage increasingly complex and multifactorial immune responses. First, the targeting of specific individual cytokines is discussed, both in terms of delivering the cytokines or blocking agents, and in terms of active immunotherapies that raise neutralizing immune responses against such single cytokine targets. Next, non-biological complex drugs such as randomized polyamino acid copolymers are discussed in terms of their ability to raise multiple different therapeutic immune responses, particularly in the context of autoimmunity. Last, biologically derived matrices and materials are discussed in terms of their ability to raise complex immune responses in the context of tissue repair. Collectively, these examples reflect the tremendous diversity of existing approaches and the breadth of opportunities that remain for generating therapeutic immune responses using biomaterials.

摘要

用于引发治疗性免疫反应的生物材料已成为一个复杂且活跃的领域。从历史上看,疫苗主要是为对抗传染病而研发的,但近年来,免疫活性生物材料已朝着越来越多的非传染病和病症发展,包括炎症、自身免疫、伤口、癌症等。本综述围绕从单靶点策略到引发日益复杂和多因素免疫反应的策略的进展来构建对这些方法的讨论。首先,讨论了针对特定单个细胞因子的靶向,包括递送细胞因子或阻断剂,以及引发针对此类单细胞因子靶点的中和免疫反应的主动免疫疗法。接下来,讨论了非生物复合药物,如随机聚氨基酸共聚物,就其引发多种不同治疗性免疫反应的能力而言,特别是在自身免疫的背景下。最后,讨论了生物衍生的基质和材料在组织修复背景下引发复杂免疫反应的能力。总体而言,这些例子反映了现有方法的巨大多样性以及使用生物材料产生治疗性免疫反应仍存在的广泛机会。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aed5/5606982/cdaf4854c604/nihms871372f6.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aed5/5606982/1b01d6b72431/nihms871372f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aed5/5606982/cdaf4854c604/nihms871372f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aed5/5606982/8c24addf542a/nihms871372f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aed5/5606982/9ecf5dd38686/nihms871372f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aed5/5606982/6a53c8f98f5d/nihms871372f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aed5/5606982/23c1e04c7176/nihms871372f4.jpg
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