期刊文献+

LAP^+CD4^+T细胞的研究进展

Advances in the research of LAP^+CD4^+T cells
下载PDF
导出
摘要 调节性T细胞是机体维持自身稳定的重要组成部分,对免疫反应具有抑制效应,在阻止自身免疫反应和维持机体免疫平衡等方面均具有重要作用。现在已发现不同的具有调节功能的T细胞亚群,如CD4+CD25+T细胞、Th3细胞和Tr1细胞等,这些T细胞多通过产生具有抑制功能的细胞因子,如IL-10和TGF-β等发挥免疫抑制效应。LAP+CD4+T细胞是近年发现的一种新的调节性T细胞亚群,在体内外实验中被证实具有免疫抑制作用,它通常以依赖TGF-β和IL-10等细胞因子的方式来发挥作用,且在一些疾病的动物模型中它影响着疾病的发生、发展,如自身免疫性疾病,炎症型疾病等。较少的研究提示LAP+CD4+T细胞在癌症病人中具有促进肿瘤进展的作用。 Having a suppressive effect on immune response , regulatory T cells (Tregs) play an important role in the maintenance of homeostasis. Treg cells are necessary both to maintain self- tolerance and prevent the onset of autoimmune disease. The Treg cells studied previously were mainly divided into three subpopulations : CD4+CD25+T cells, Th3 cells and Tr1 cells. These T cells exert the immune suppressive function by producing some kinds of cytokines , such as IL-10 and TGF-β, with the ability of immune suppressive. Recently , LAP+CD4+T cells have been identified as a new subset of Treg cells and a population with regulatory function both in vitro and in vivo. This regulatory function is partly mediated by TGF-β and IL-10. In animal experiments , these cells have been shown to affect the genesis and development of some diseases , such as autoimmune disorder and inflammatory disease. A few researches implied that these cells also play an important role in tumor progression in patients with cancer.
出处 《岭南现代临床外科》 2013年第3期249-252,共4页 Lingnan Modern Clinics in Surgery
基金 深圳市科技计划项目(JC200903180670A 201103023)
关键词 LAP+CD4+T细胞 调节性T细胞 转化生长因子-Β LAP+CD4+T cells Regulatory T cells Transforming growth factor-β
  • 相关文献

参考文献25

  • 1Hoglund P. Induced peripheral regulatory T cells: the family grows larger [J]. Eur J Immunol, 2006, 36(2) : 264-266.
  • 2Miyara M, Sakaguehi S. Natural regulatory T cells: mechanisms of suppression [J]. Trends Mal Med, 2007,13(3) : 108-116.
  • 3Fife BT, Bluestone JA. Control of peripheral T-cell tolerance and autoimmunity via the CTLA-4 and PD-1 pathways[J]. Imm- unol Rev, 2008, 224: 166-182.
  • 4Miyazono K, Iehijo H, Heldin CH. Transforming growth factor- beta: latent forms, binding proteins and receptors [J]. Growth Factors, 1993, 8(1): 11-22.
  • 5Coombes JL, Siddiqui KR, Arancibia-C6rcamo CV, et al. A functionally specialized population of mucosal CD103 + DCs induces Foxp3 + regulatory T cells via a TGF-beta and retinoic acid-dependent mechanism [J]. I Exp Med, 2007, 204(8): 1757-1764.
  • 6Liu Y, Zhang P, Li J, et al. A critical function for TGF- beta signaling in the development of natural CD4 +CD25 + Foxp3 + regulatory T cells [ J ]. Nat Immunol, 2008, 9 (6) : 632-640.
  • 7Keski-Oja J, Koli K, von Melchner H. TGF-beta activation by traction [J]? Trends Cell Biol, 2004, 14(12): 657- 659.
  • 8McMahon GA, Dignam JD, Gentry LE. Structural characteri- zation of the latent complex between transforming growth factor beta 1 and beta 1-latency-associated peptide[J]. Biochem J, 1996, 313( Pt 1): 343-351.
  • 9Ribeiro SM, Poczatek M, Schultz-Cherry S, et al. The activation sequence of thrombospondin-1 interacts with the latency-associated peptide to regulate activation of latent transforming growth factor-beta [J]. J Biol Chem, 1999, 274 (19) : 13586-13593.
  • 10Oida T, Zhang X, Goto M, et al. CD4+CD25- T cells that express latency-associated peptide on the surface suppress CD4 +CD45RBhigh-induced colitis by a TGF-beta-dependent mechanism [J]. J Immunol, 2003, 170(5) : 2516-2522.

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部