• 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

口服耐受在自身免疫性疾病治疗中的应用——主动抑制和旁观者抑制

[Application of oral tolerance to the treatment of autoimmune diseases--active suppression and bystander suppression].

作者信息

Matsui M

机构信息

Department of Internal Medicine, Saga Medical School.

出版信息

Nihon Rinsho. 1997 Jun;55(6):1537-42.

PMID:9200945
Abstract

Oral tolerance is a phenomenon in which an orally ingested antigen induces systemic hyporesponsiveness to the same antigen. If the mechanism can be applied to autoantigens, it could be a promising mode of antigen-specific immunomodulatory treatment for patients with autoimmune diseases. Multiple ingestion of low doses of antigen induces active suppression. Under this condition, suppression of autoimmune attack to target tissues is mediated by anti-inflammatory cytokines such as TGF-beta, which are released from regulatory T cells triggered antigen-specifically. This type of oral tolerance, termed "bystander suppression", has one advantage of needing to know only the major components of the target tissue instead of exact epitopes of autoimmunity. Utilizing this mechanism, clinical trials of oral tolerance therapy are going on among the patients with multiple sclerosis, rheumatoid arthritis, and uveitis.

摘要

口服耐受是一种现象,即经口服摄入的抗原可诱导机体对同一抗原产生全身性低反应性。如果该机制能够应用于自身抗原,那么它可能成为一种针对自身免疫性疾病患者的、具有前景的抗原特异性免疫调节治疗方式。多次低剂量摄入抗原可诱导主动抑制。在此条件下,对靶组织自身免疫攻击的抑制由抗炎细胞因子(如转化生长因子-β)介导,这些细胞因子由抗原特异性触发的调节性T细胞释放。这种类型的口服耐受,称为“旁观者抑制”,具有一个优点,即只需要了解靶组织的主要成分,而无需知道自身免疫的确切表位。利用这一机制,口服耐受疗法的临床试验正在多发性硬化症、类风湿性关节炎和葡萄膜炎患者中进行。

相似文献

1
[Application of oral tolerance to the treatment of autoimmune diseases--active suppression and bystander suppression].口服耐受在自身免疫性疾病治疗中的应用——主动抑制和旁观者抑制
Nihon Rinsho. 1997 Jun;55(6):1537-42.
2
Oral tolerance: immunologic mechanisms and treatment of animal and human organ-specific autoimmune diseases by oral administration of autoantigens.口服耐受:通过口服自身抗原对动物和人类器官特异性自身免疫性疾病的免疫机制及治疗
Annu Rev Immunol. 1994;12:809-37. doi: 10.1146/annurev.iy.12.040194.004113.
3
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.
4
Oral tolerance for the treatment of autoimmune diseases.口服耐受用于自身免疫性疾病的治疗。
Annu Rev Med. 1997;48:341-51. doi: 10.1146/annurev.med.48.1.341.
5
Oral tolerance: therapeutic implications for autoimmune diseases.口服耐受:自身免疫性疾病的治疗意义。
Clin Dev Immunol. 2006 Jun-Dec;13(2-4):143-57. doi: 10.1080/17402520600876804.
6
Oral tolerance: immune mechanisms and the generation of Th3-type TGF-beta-secreting regulatory cells.口服耐受:免疫机制与分泌Th3型转化生长因子β的调节性细胞的产生
Microbes Infect. 2001 Sep;3(11):947-54. doi: 10.1016/s1286-4579(01)01456-3.
7
[Collagen in the treatment of rheumatic diseases--oral tolerance].[胶原蛋白在风湿性疾病治疗中的应用——口服耐受]
Bratisl Lek Listy. 1999;100(10):567-71.
8
Oral tolerance for treating uveitis - new hope for an old immunological mechanism.口服耐受治疗葡萄膜炎——古老免疫机制带来新希望
Prog Retin Eye Res. 2002 Nov;21(6):577-89. doi: 10.1016/s1350-9462(02)00039-3.
9
Epitopes of myelin basic protein that trigger TGF-beta release after oral tolerization are distinct from encephalitogenic epitopes and mediate epitope-driven bystander suppression.口服耐受后触发转化生长因子-β释放的髓鞘碱性蛋白表位与致脑炎性表位不同,并介导表位驱动的旁观者抑制。
J Immunol. 1993 Dec 15;151(12):7307-15.
10
Oral tolerance.口服耐受
Rev Immunogenet. 2000;2(1):61-73.

引用本文的文献

1
Coupling of oral human or porcine insulin to the B subunit of cholera toxin (CTB) overcomes critical antigenic differences for prevention of type I diabetes.将人源或猪源口服胰岛素与霍乱毒素(CTB)的B亚基偶联,可克服关键的抗原差异,从而预防I型糖尿病。
Clin Exp Immunol. 2003 Oct;134(1):38-45. doi: 10.1046/j.1365-2249.2003.02255.x.