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Graves病患者外周血OX40和OX40L分子表达的研究 被引量:2

The expression of OX40 and OX40L in the peripheral blood of Graves disease patients
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摘要 探讨OX40和OX40L分子在Graves病患者外周血T淋巴细胞和单核细胞上的表达及其在Graves病发病机制中的可能作用。采用流式细胞仪检测技术对50例初发Graves病患者和30例健康志愿者外周血T细胞上OX40和单核细胞上OX40L的表达水平进行分析,并对28例治疗前后病人淋巴细胞上OX40/OX40L的表达进行了比较。结果:与正常对照组比,初发Graves病患者外周血CD4+T细胞上OX40表达水平明显升高,而CD8+T细胞上OX40表达水平无显著变化;同时,还检测到单核细胞上OX40L表达水平也明显增加。治疗后,FT3(游离三碘甲腺原氨酸)值恢复至健康对照组表达范围的Graves病患者其CD4+T细胞上OX40和单核细胞上OX40L的表达均显著降低至正常水平;而FT3值仍偏高的患者单核细胞上OX40L的表达降低,但未降至健康对照组表达范围,CD4+T细胞上OX40的表达则无显著变化。Graves病患者外周血T细胞和单核细胞上分别存在OX40和OX40L的异常表达,且与治疗效果密切相关,提示OX40/OX40L信号在T细胞与单核细胞相互作用过程中可能有助于自身反应性T细胞的持续活化,从而参与Graves病的免疫发生发展。 To investigate the expression of OX40 and OX40L molecules in peripheral blood T lymphocytes and mononuclear cells in Graves' disease and their possible roles in the pathogenesis.OX40 and OX40L expression on T cells and mononuclear cells were detected by flow cytometry in 50 cases of Graves' disease patients and 30 healthy volunteers.Twenty eight samples from the patients were examined both before and after therapy to analyzed the changes of OX40/OX40L expression.Compare with the healthy control group,the expression of OX40 on CD4+ T cells and OX40L expression on monocytes in Graves' disease patients was significantly upregulated,while OX40 on CD8+ T cells had no significant change in expression level.After therapy,the patients whose FT3 levels resumed normal,their OX40 expression on CD4+ T cell and OX40L expression on monocytes returned toward normal,those whose FT3 levels didn't resume normal,OX40 and OX40L expression on CD4+ T cells and monocytes didn't return toward normal.OX40 and OX40L were abnormally expressed on CD4+ T cells and mononuclear cells in the peripheral blood of Graves' disease and their expressions were correlated with theraputic effects,suggesting that OX40/OX40L signal may contribute to the prolonged activation of T cells,which participate in the development of Graves' disease.
出处 《现代免疫学》 CAS CSCD 北大核心 2012年第1期36-40,共5页 Current Immunology
基金 国家自然科学基金资助项目(30930085 81072451)
关键词 GRAVES病 OX40 OX40L Graves disease co-stimulatory molecule OX40 OX40L
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参考文献13

  • 1Zaletel K,Krhin B,Gaberscek S,et al.The influence of theexon 1polymorphism of the cytotoxic T lymphocyte antigen 4gene on thyroid antibody production in patients with newly di-agnosed Gravesdisease[J].J Thyroid,2002,12:373-376.
  • 2Furugaki K,Shirasawa S,Ishikawa N,et al.Association ofthe T-cell regulatory gene CTLA4with Gravesdisease andautoimmune thyroid disease in the Japanese[J].J Hum Gen-et,2004,49:166-168.
  • 3Bossowski A,Stasiak-Barmuta A,Urban M,et al.Analysisof costimulatory molecules(CD28-CTLA-4/B7)expressionon chosen mononuclear cells in adolescents with Gravesdis-ease during methimazole therapy[J].Endoktynol DiabetolChor Przemiany Materii Wieku Rozw,2004,10:93-101.
  • 4Bossowski A,Stasiak-Barmuta A,Urban M.Relationshipbetween CTLA-4and CD28 molecule expression on T lym-phocytes and stimulating and blocking autoantibodies to theTSH-receptor in children with Gravesdisease[J].HormRes,2005,64:189-197.
  • 5Croft M,So T,Duan W,et al.The significance of OX40andOX40Lto T-cell biology and immune disease[J].ImmunolRev,2009,229:173-191.
  • 6Ishii N,Takahashi T,Soroosh P,et al.OX40-OX40ligandinteraction in T-cell mediated immunity and immunopathology[J].Adv Immunol,2010,105:63-98.
  • 7张季平 邓伟吾 周玉淑.临床内科学[M].天津:天津科学技术出版社,2000.1660-1663.
  • 8Murata K,Ishii N,Takano H,et al.Impairent of antigen-presenting cell function in mice lacking expression of OX40ligand[J].J Exp Med,2001,191:365-374.
  • 9Kashiwakura J,Yokoi H,Saito H,et al.T cell proliferationby directcross-talk between OX40ligand on human mast cellsand OX40on human T cells:Comparison of gene expressionprofiles between human tonsillar and lung-cultured mast cells[J].J Immunol,2004,173:5247-5257.
  • 10Nakae S,Suto H,Iikura M,et al.Mast cells enhance T cellactivation:importance of mast cell costimulatory moleculesand secreted TNF[J].J Immunol,2006,176:2238-2248.

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同被引文献20

  • 1Yu Fu,Qing Lin,Zhirong Zhang,Ling Zhang.Therapeutic strategies for the costimulatory molecule OX40 in T-cell-mediated immunity[J].Acta Pharmaceutica Sinica B,2020,10(3):414-433. 被引量:28
  • 2张飚,唐福林.系统性红斑狼疮模型鼠MRL/lpr研究进展[J].中华风湿病学杂志,2006,10(2):110-113. 被引量:27
  • 3Perl A. Pathogenic mechanisms in systemic lupus erythema- tosus [J]. Autoimmunity, 2010,43 : 1-6.
  • 4Crispin JC, Kyttaris VC, Terhorst C, etal. T cells as thera- peutic targets in SLE[J]. Nat Rev Rheumatol, 2010,6: 317- 325.
  • 5Jenks SA, Sanz I. Altered B cell receptor signaling in human systemic lupus erythematosus [J]. Autoimmun Rev, 2009, 8:209-213.
  • 6Moon JJ, Chu HH, Pepper M, eta& Naive CD4+T cell fre quency varies for different epitopes and predicts repertoire di- versity and response magnitude [J]. Immunity, 2007, 27: 203-213.
  • 7Bossowski A, Stasiak-Barmuta A, Urban M. Relationship between CTLA-4 and CD28 molecule expression on T lym- phocytes and stimulating and blocking autoantibodies to the TSH-receptor in children with Graves' disease [J]. Horm Res, 2005,64:189-197.
  • 8So T, Lee SW, Croft M. Immune regulation and control of regulatory T cells by OX40 and 4-1BB[J]. Cytokine Growth Factor Rev, 2008,19:253- 262.
  • 9Croft M, So T, Duan W, etal. The significance of OX40 and OX40L to T-cell Biology and immune disease[J]. Immunol Rev, 2009,229:173 -191.
  • 10Patschan S, Dolff S, Kribben A, et al. CD134 expression on CD4+ T cells is associated with nephritis and disease activity in patients with systemic lupus erythematosus [J]. Clin Exp Immunol, 2006,145 : 235-242.

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