工程化抗原递呈细胞用于自身免疫的免疫疗法。

IF 15.2 1区 医学 Q1 PHARMACOLOGY & PHARMACY
Clinton T. Smith , Zhenyu Wang , Jamal S. Lewis
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引用次数: 0

摘要

自身免疫性疾病是一种负担沉重的疾病,影响着全球相当一部分人口。自身免疫性疾病的特征是宿主的免疫系统被授权根据特定抗原攻击其组织。目前还没有治疗自身免疫性疾病的方法。目前治疗自身免疫性疾病的临床标准是服用免疫抑制剂,这种药物会削弱免疫系统,减少自身炎症反应。然而,自身免疫性疾病患者会产生毒性,无法产生足够的免疫反应来抵御病原体,而且更容易发生感染。因此,人们正齐心协力开发更有效的方法,针对抗原递呈细胞进行免疫调节治疗,因为抗原递呈细胞参与调节对特定抗原的免疫反应。在本综述中,我们将重点介绍目前正在开发的以抗原递呈细胞为靶点、改善自身免疫性疾病治疗效果的方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Engineering antigen-presenting cells for immunotherapy of autoimmunity

Engineering antigen-presenting cells for immunotherapy of autoimmunity

Autoimmune diseases are burdensome conditions that affect a significant fraction of the global population. The hallmark of autoimmune disease is a host’s immune system being licensed to attack its tissues based on specific antigens. There are no cures for autoimmune diseases. The current clinical standard for treating autoimmune diseases is the administration of immunosuppressants, which weaken the immune system and reduce auto-inflammatory responses. However, people living with autoimmune diseases are subject to toxicity, fail to mount a sufficient immune response to protect against pathogens, and are more likely to develop infections. Therefore, there is a concerted effort to develop more effective means of targeting immunomodulatory therapies to antigen-presenting cells, which are involved in modulating the immune responses to specific antigens. In this review, we highlight approaches that are currently in development to target antigen-presenting cells and improve therapeutic outcomes in autoimmune diseases.

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来源期刊
CiteScore
28.10
自引率
5.00%
发文量
294
审稿时长
15.1 weeks
期刊介绍: The aim of the Journal is to provide a forum for the critical analysis of advanced drug and gene delivery systems and their applications in human and veterinary medicine. The Journal has a broad scope, covering the key issues for effective drug and gene delivery, from administration to site-specific delivery. In general, the Journal publishes review articles in a Theme Issue format. Each Theme Issue provides a comprehensive and critical examination of current and emerging research on the design and development of advanced drug and gene delivery systems and their application to experimental and clinical therapeutics. The goal is to illustrate the pivotal role of a multidisciplinary approach to modern drug delivery, encompassing the application of sound biological and physicochemical principles to the engineering of drug delivery systems to meet the therapeutic need at hand. Importantly the Editorial Team of ADDR asks that the authors effectively window the extensive volume of literature, pick the important contributions and explain their importance, produce a forward looking identification of the challenges facing the field and produce a Conclusions section with expert recommendations to address the issues.
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