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针对自身免疫的抗原特异性治疗方法。

Antigen-specific therapeutic approaches for autoimmunity.

机构信息

Institut D'Investigacions Biomèdiques August Pi i Sunyer, Barcelona, Spain.

Julia McFarlane Diabetes Research Centre (JMDRC) and Department of Microbiology, Immunology and Infectious Diseases, Snyder Institute for Chronic Diseases, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada.

出版信息

Nat Biotechnol. 2019 Mar;37(3):238-251. doi: 10.1038/s41587-019-0015-4. Epub 2019 Feb 25.

DOI:10.1038/s41587-019-0015-4
PMID:30804535
Abstract

The main function of the immune system in health is to protect the host from infection by microbes and parasites. Because immune responses to nonself bear the risk of unleashing accidental immunity against self, evolution has endowed the immune system with central and peripheral mechanisms of tolerance, including regulatory T and B cells. Although the past two decades have witnessed the successful clinical translation of a whole host of novel therapies for the treatment of chronic inflammation, the development of antigen-based approaches capable of selectively blunting autoimmune inflammation without impairing normal immunity has remained elusive. Earlier autoantigen-specific approaches employing peptides or whole antigens have evolved into strategies that seek to preferentially deliver these molecules to autoreactive T cells either indirectly, via antigen-presenting cells, or directly, via major histocompatibility complex molecules, in ways intended to promote clonal deletion and/or immunoregulation. The disease specificity, mechanistic underpinnings, developability and translational potential of many of these strategies remain unclear.

摘要

免疫系统在健康中的主要功能是保护宿主免受微生物和寄生虫的感染。由于对非自身的免疫反应有引发针对自身的意外免疫的风险,进化赋予了免疫系统中枢和外周耐受机制,包括调节性 T 和 B 细胞。尽管在过去的二十年中,已经成功地将许多新型治疗慢性炎症的疗法应用于临床,但开发出能够选择性地抑制自身免疫性炎症而不损害正常免疫的抗原为基础的方法仍然难以实现。早期采用肽或全抗原的自身抗原特异性方法已经演变成旨在通过抗原呈递细胞间接或通过主要组织相容性复合物分子直接将这些分子递送给自身反应性 T 细胞的策略,以促进克隆删除和/或免疫调节。这些策略中的许多策略的疾病特异性、机制基础、可开发性和转化潜力仍然不清楚。

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2
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Nat Immunol. 2018 May;19(5):497-507. doi: 10.1038/s41590-018-0083-5. Epub 2018 Apr 16.
3
Tolerogenic Nanoparticles Induce Antigen-Specific Regulatory T Cells and Provide Therapeutic Efficacy and Transferrable Tolerance against Experimental Autoimmune Encephalomyelitis.
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Int J Mol Sci. 2025 Jul 4;26(13):6453. doi: 10.3390/ijms26136453.
4
Regulated cell death and DAMPs as biomarkers and therapeutic targets in normothermic perfusion of transplant organs. Part 2: implementation strategies.作为移植器官常温灌注生物标志物和治疗靶点的程序性细胞死亡和损伤相关分子模式。第2部分:实施策略。
Front Transplant. 2025 Apr 24;4:1575703. doi: 10.3389/frtra.2025.1575703. eCollection 2025.
5
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World J Gastroenterol. 2025 Apr 14;31(14):104397. doi: 10.3748/wjg.v31.i14.104397.
6
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Nat Biomed Eng. 2025 Mar 28. doi: 10.1038/s41551-025-01373-0.
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