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树突细胞在类风湿性关节炎病理机制中的免疫原性和耐受性双重作用 被引量:7

Dual role of dendritic cells in the pathological mechanism of rheumatoid arthritis: immunogenicity and tolerogenicity
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摘要 树突细胞(dendritic cells,DCs)是体内功能最强大的专职抗原提呈细胞(antigen-presenting cell,APC),具有免疫原性和耐受性双重作用。DCs的免疫原性体现在作为专职APC对自身抗原异常提呈,引起机体免疫系统紊乱,是参与类风湿关节炎(rheumatoid arthritis,RA)发生的一个重要原因;DCs的耐受性则体现在通过多种机制诱导抗原特异性T细胞消除、无能及调节性T细胞(regulatory T cells,Tregs)的产生,导致免疫耐受,发挥对RA的调控作用。该文结合该课题组的研究结果对DCs参与RA的发病机制以及在RA病理机制中的调控作用方面进行介绍和评论。 Dendritic cells (DCs) are the most powerful professional antigen presenting cell (APC) , which have immunogenic and tolerogenic function in immune system. As a professional APC, the immunogenic DC presents self-antigen abnormally and results in immune system disorder. The immunogenie function may be one pathogenesis of RA. On the other hand, the tolerogenicity of DC could induce antigen specific T cell deletion, an-ergy and produce regulatory T cells (Tregs), which make DCs play a regulatory role in RA. This paper makes an introduction about how DCs are involved and play a regulatory role in the pathogenesis of RA.
出处 《中国药理学通报》 CAS CSCD 北大核心 2012年第9期1185-1188,共4页 Chinese Pharmacological Bulletin
基金 国家自然科学基金资助项目(No 30973543,31100640,81173075) 安徽省自然科学基金资助项目(No11040606M195)
关键词 树突细胞 免疫原性 耐受性 类风湿性关节炎 病理机制 双重作用 dendritic cells immunogenicity tolerogenicity rheumatoid arthritis pathological mechanism dual role
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  • 1彭桉平,曾耀英,俞瑜,肇静娴,狄静芳.紫杉醇对小鼠T细胞CD69、CD25表达及增殖作用的流式细胞术分析[J].中国药理学通报,2005,21(6):705-707. 被引量:5
  • 2Cope A P,SchulzerKoops H, Aringer M. The central role of T cells in rheumatoid arthritis[ J]. Clin Exp Rheumatol,2007 ,25 :4 - 11.
  • 3Sakaguchi S, Sakaguchi N, Asano M, et al. Immunologic self-tolerance maintained by activated T cells expressing IL-2 receptor alpha-chains ( CD25 ). Breakdown of a single mechanism of self-tolerance causes various autoimmune diseases[ J]. J Immunol, 1995, 155,1151 -64.
  • 4Turka L A,Walsh P T. IL-2 signaling and CD4^+ CD25^+ Foxp3^+ regulatory T cells [ J ]. Front Biosci, 2008,13 : 1440 - 6.
  • 5Piccirillo C A,Shevach E M. Cutting edge:control of CD8^+ T cell activation by CD4^+ CD25^+ immunoregulatory cells [ J ]. J Immunol,2001,167 : 1137 - 40.
  • 6ZwarT D,Read S,van Driel I R,Gleeson P A. CD4^+ CD25^+ regulatory T cells inhibit the antigen-dependent expansion of self-reactive T cells in vivo [ J ]. J Immunol , 2006 ,176 : 1609 - 17.
  • 7D'Cruz L M, Klein L. Development and function of agonist-induced CD25^+ Foxp3^+ regulatory T ceils in the absence of interleukin 2 signaling [ J ]. Nat Immunol,2005,6 : 1152 - 9.
  • 8Takahashi T, Tagami T, Yamazaki S, et al. Immunologic selftolerance maintained by CD25^(+) CD4^(+) regulatory T cells constitutively expressing cytotoxic T lymphocyte-associated antigen 4[ J]. J Exp Med,2000,192:303 - 10.
  • 9Read S, Malmstrom V, Powrie F. Cytotoxic T lymphocyte-associated antigen 4 plays an essential role in the function of CD25^+ CD4^+ regulatory ceils that control intestinal inflammation [ J ]. J Exp Med ,2000,192:295 - 302.
  • 10Fontenot J D,Gavin M A,Rudensky A Y. Foxp3 programs the development and function of CD4^+ CD25^+ regulatory. T cells[ J]. Nat Immunol,2003,4:330 - 6.

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