• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

用于预防和治疗自身免疫性疾病的抗原特异性耐受策略。

Antigen-specific tolerance strategies for the prevention and treatment of autoimmune disease.

作者信息

Miller Stephen D, Turley Danielle M, Podojil Joseph R

机构信息

Department of Microbiology-Immunology and Interdepartmental Immunobiology Center, Northwestern University Feinberg School of Medicine, Chicago, Illinois 60611, USA.

出版信息

Nat Rev Immunol. 2007 Sep;7(9):665-77. doi: 10.1038/nri2153. Epub 2007 Aug 10.

DOI:10.1038/nri2153
PMID:17690713
Abstract

The development of safe and effective antigen-specific therapies is needed to treat patients with autoimmune diseases. These therapies must allow for the specific tolerization of self-reactive immune cells without altering host immunity to infectious insults. Experimental models and clinical trials for the treatment of autoimmune disease have identified putative mechanisms by which antigen-specific therapies induce tolerance. Although advances have been made in the development of efficient antigen-specific therapies, translating these therapies from bench to bedside has remained difficult. Here, we discuss the recent advances in our understanding of antigen-specific therapies for the treatment of autoimmune diseases.

摘要

需要开发安全有效的抗原特异性疗法来治疗自身免疫性疾病患者。这些疗法必须能够使自身反应性免疫细胞产生特异性耐受,同时又不改变宿主对感染性侵害的免疫力。治疗自身免疫性疾病的实验模型和临床试验已经确定了抗原特异性疗法诱导耐受的推定机制。尽管在高效抗原特异性疗法的开发方面已经取得了进展,但将这些疗法从实验室转化到临床应用仍然困难重重。在此,我们讨论了在理解用于治疗自身免疫性疾病的抗原特异性疗法方面的最新进展。

相似文献

1
Antigen-specific tolerance strategies for the prevention and treatment of autoimmune disease.用于预防和治疗自身免疫性疾病的抗原特异性耐受策略。
Nat Rev Immunol. 2007 Sep;7(9):665-77. doi: 10.1038/nri2153. Epub 2007 Aug 10.
2
Immunological mechanisms involved in experimental peptide immunotherapy of T-cell-mediated diseases.T细胞介导疾病的实验性肽免疫疗法中涉及的免疫机制。
Crit Rev Immunol. 2000;20(6):451-69.
3
Does our current understanding of the molecular basis of immune tolerance predict new therapies for autoimmune disease?我们目前对免疫耐受分子基础的理解能否预测出自身免疫性疾病的新疗法?
Nat Clin Pract Rheumatol. 2006 Sep;2(9):491-9. doi: 10.1038/ncprheum0272.
4
Antigen-specific therapies in multiple sclerosis.多发性硬化症中的抗原特异性疗法。
Int Rev Immunol. 2005 Sep-Dec;24(5-6):393-413. doi: 10.1080/08830180500371256.
5
Dendritic cells in tolerance induction for the treatment of autoimmune diseases.树突状细胞在诱导免疫耐受治疗自身免疫性疾病中的作用。
Eur J Immunol. 2010 Aug;40(8):2119-23. doi: 10.1002/eji.201040474.
6
Design of effective immunotherapy for human autoimmunity.针对人类自身免疫性疾病的有效免疫疗法设计。
Nature. 2005 Jun 2;435(7042):612-9. doi: 10.1038/nature03727.
7
[Autoimmunity].[自身免疫]
Schweiz Med Wochenschr. 1997 Mar 1;127(9):333-40.
8
Treating autoimmune diseases through restoration of antigen-specific immune tolerance.通过恢复抗原特异性免疫耐受来治疗自身免疫性疾病。
Arch Immunol Ther Exp (Warsz). 2006 Jan-Feb;54(1):1-13. doi: 10.1007/s00005-006-0001-7. Epub 2006 Jan 23.
9
Oral tolerance: elucidation of mechanisms and application to treatment of autoimmune diseases.口服耐受:机制解析及其在自身免疫性疾病治疗中的应用
Biopolymers. 1997;43(4):323-35. doi: 10.1002/(SICI)1097-0282(1997)43:4<323::AID-BIP5>3.0.CO;2-X.
10
Antigen-specific therapies in multiple sclerosis: going beyond proteins and peptides.多发性硬化症中的抗原特异性疗法:超越蛋白质和肽类。
Int Rev Immunol. 2005 Sep-Dec;24(5-6):415-46. doi: 10.1080/08830180500379655.

引用本文的文献

1
A Semi-Mechanistic Mathematical Model of Immune Tolerance Induction to Support Preclinical Studies of Human Monoclonal Antibodies in Rats.一种用于支持大鼠体内人单克隆抗体临床前研究的免疫耐受诱导半机制数学模型。
Pharmaceutics. 2025 Jun 27;17(7):845. doi: 10.3390/pharmaceutics17070845.
2
Lipid nanoparticles from Walp mitigate sepsis through multimodal protein corona formation.来自Walp的脂质纳米颗粒通过多模态蛋白质冠层形成减轻败血症。
Mol Ther Methods Clin Dev. 2025 May 14;33(2):101491. doi: 10.1016/j.omtm.2025.101491. eCollection 2025 Jun 12.
3
Generation of tolerogenic antigen-presenting cells in vivo via the delivery of mRNA encoding PDL1 within lipid nanoparticles.
通过在脂质纳米颗粒中递送编码程序性死亡受体配体1(PDL1)的信使核糖核酸(mRNA)在体内生成耐受性抗原呈递细胞。
Nat Biomed Eng. 2025 Mar 28. doi: 10.1038/s41551-025-01373-0.
4
Biodegradable Polymers for Application as Robust Immunomodulatory Biomaterial Carrier Systems.用作强大免疫调节生物材料载体系统的可生物降解聚合物。
Small. 2025 Feb 16:e2409422. doi: 10.1002/smll.202409422.
5
Anti-Inflammatory Macrophage-Derived Exosomes Modified With Self-Antigen Peptides for Treatment of Experimental Autoimmune Encephalomyelitis.用自身抗原肽修饰的抗炎巨噬细胞衍生外泌体治疗实验性自身免疫性脑脊髓炎
Adv Sci (Weinh). 2025 Apr;12(13):e2415265. doi: 10.1002/advs.202415265. Epub 2025 Feb 12.
6
Autoimmunity-Associated SNP rs3024505 Disrupts STAT3 Binding in B Cells, Leading to IL10 Dysregulation.自身免疫相关 SNP rs3024505 破坏 B 细胞中的 STAT3 结合,导致 IL10 失调。
Int J Mol Sci. 2024 Sep 23;25(18):10196. doi: 10.3390/ijms251810196.
7
Harnessing the potential of the NALT and BALT as targets for immunomodulation using engineering strategies to enhance mucosal uptake.利用 NALT 和 BALT 的潜力,通过工程策略作为免疫调节的靶点,以增强黏膜摄取。
Front Immunol. 2024 Sep 2;15:1419527. doi: 10.3389/fimmu.2024.1419527. eCollection 2024.
8
Cell-drug conjugates.细胞药物偶联物。
Nat Biomed Eng. 2024 Nov;8(11):1347-1365. doi: 10.1038/s41551-024-01230-6. Epub 2024 Jul 1.
9
Development of protein-polymer conjugate nanoparticles for modulation of dendritic cell phenotype and antigen-specific CD4 T cell responses.用于调节树突状细胞表型和抗原特异性CD4 T细胞反应的蛋白质-聚合物共轭纳米颗粒的研发。
ACS Appl Polym Mater. 2023 Nov 10;5(11):8794-8807. doi: 10.1021/acsapm.3c00548. Epub 2023 Oct 9.
10
Peptide Drugs: Current Status and it's Applications in the Treatment of Various Diseases.肽类药物:现状及其在各种疾病治疗中的应用。
Curr Drug Res Rev. 2024;16(3):381-394. doi: 10.2174/0125899775295960240406073630.