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B7-H4在类风湿关节炎组织内的表达及分布研究 被引量:7

Expression and distribution of the costimulatory molecule B7-H4 in tissues from rheumatoid arthritis
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摘要 为探讨共刺激分子B7-H4在牛Ⅱ型胶原(CⅡ)诱导的类风湿关节炎(CIA)模型小鼠免疫器官、关节及RA患者滑膜组织内的表达,使用牛Ⅱ型胶原免疫DBA-1/j小鼠,建立小鼠类风湿关节炎模型。免疫组化检测B7-H4的表达变化,结果证实小鼠的胸腺、脾脏及淋巴结中有大量的B7-H4阳性细胞,免疫荧光分析结果表明这些B7-H4+细胞主要为CD31+内皮细胞。统计分析表明,CIA小鼠体内免疫器官中B7-H4表达及分布相对于对照组小鼠没有显著提高,但是RA患者及CIA小鼠的滑膜组织内发现大量B7-H4阳性细胞。鉴于关节炎滑膜组织内有大量B7-H4阳性细胞,提示其有可能参与并调节了关节炎的病理进程。 The expression and distribution of B7-H4 protein in tissues from bovine collagen II(CII)-induced mouse rheumatoid arthritis(CIA) and synovial tissues of RA patients was detected and analyzed by immunohistochemistry,in which the fluorescence double-staining was further used to characterize B7-H4 expression.Immunohistochemical analysis revealed that B7-H4 positive cells were found in thymus,spleen,lymph nodes and bone marrow,and fluorescence double-staining further demonstrated that B7-H4 positive cells were CD31+ endothelial cells.However,the expression and distribution of B7-H4 was not changed significantly between normal and CIA mice.Interestingly,high level of B7-H4 positive cells was found both in synovial tissues of CIA mice and RA patients.The expression of B7-H4 was observed on the surface of antigen presentation cells,such as endothelial cells within immune organs and synovial tissues of CIA mice and RA patients,indicated this signal might be involved in regulating local T cell activation and finally participated in the pathogenesis of RA.
出处 《现代免疫学》 CAS CSCD 北大核心 2011年第2期130-134,共5页 Current Immunology
基金 国家自然科学基金资助项目(30700855 60971117)
关键词 B7-H4 类风湿关节炎 滑膜组织 免疫器官 免疫组化 B7-H4 rheumatoid arthritis synovial tissues immune organs immunohistochemistry
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参考文献15

  • 1Goekoop Ruiterman YP, Huizinga TW . Rheumatoid arthritis: can we achieve true drug-free remission in patients with RA[J]. Nat RevRheumatol, 2010,6:68-70.
  • 2McInnes IB, Schett G. Cytokines in the pathogenesis of rheumatoid arthritis[J]. Nat Rev Immunol, 2007,7:429 -442.
  • 3Gary SF. Evolving concepts of rheumatoid arthritis[J]. Nature, 2003,423:356 -361.
  • 4SharpeAH, Abhas, AK. T cell costimulation biology, ther apeutic potential, and chaUenges[J]. N Engl J Med, 2006, 355 :973-975.
  • 5Kremer JM, Westhovens R, Leon M, et al. Treatment of rheumatoid arthritis by selective inhibition of T cell activa tion with fusion protein CTLA4Ig[J]. N Engl J Med, 2003, 349,1907- 1915.
  • 6李晓娟,胡义平,刘隽永,姜世勃,刘叔文.CD4^+CD25^+Foxp3^+调节性T细胞和类风湿关节炎的治疗[J].现代免疫学,2009,29(6):514-517. 被引量:9
  • 7Hu YL, Metz DP, Chung J, etal. B7RP-1 blockade ameliorates autoimmunity through regulation of follicular helper T cells[J]. J Immunol, 2009,182:1421-1428.
  • 8Siea, GL, Choi, IH, Zhu, G, etal. B7-H4, a molecule of the B7 family, negatively regulates T cell immunity[J]. Im munity, 2003,18:849- 861.
  • 9Zang X, Loke P, Kim J, et al. B7x: a widely expressed B7 family member that inhibits T cell activation[J]. Proc Natl Acad Sci USA, 2003,100:10388-10392.
  • 10Tringler B, Liu W, Corral L, et al. B7 H4 overexpression in ovarian tumors[J]. Gynecol Oncol, 2006,100 : 44 -52.arthritis= a mouse model informed by clinical dataEJ]. PLoS Med, 2009,6=.

二级参考文献20

  • 1焦志军,尤海燕,陈蕾,汪毅,阴晴,邵启祥.类风湿性关节炎患者CD4^+CD25^+Foxp3^+调节性T细胞检测及意义[J].中国免疫学杂志,2007,23(10):936-938. 被引量:14
  • 2陈广洁.Foxp3和CD4^+CD25^+调节性T细胞研究进展[J].国外医学(免疫学分册),2005,28(1):1-4. 被引量:15
  • 3李卫鹏,王福庆.CD4^+CD25^+ Treg的免疫调节作用机制以及临床研究进展[J].现代免疫学,2006,26(2):164-167. 被引量:18
  • 4Hori S, Nomura T, Sakaguchi S. Control of regulatory T cell development by the transcription factor Foxp3 [J]. Science,2003, 299:1057-1061.
  • 5Fontenot JD, Gavin MA, Rudensky AY. Foxp3 programs the development and function of CD4^+ CD25^+ regulatory T cells[J]. Nat Immunol, 2003, 4:330-336.
  • 6Flores Borja F, Mauri C, Ehrenstein MR. Restoring the balance: harnessing regulatory T cells for therapy in rheumatold arthritis[J]. Eur J Immunol, 2008, 38: 934-937.
  • 7Von BH. Mechanisms of suppression by suppressor T cells [J]. Nat Immunol, 2005, 6:338-344.
  • 8Sarkar S, Fox DA. Regulatory T cell defects in rheumatoid arthritis[J]. Arthritis Rheum, 2007, 56:710-713.
  • 9Niedbala W, Wei XQ, Cai B, et al. IL- 35 is a novel cytokine with therapeutic effects against collagen-induced arthritis through the expansion of regulatory T cells and suppression of Th17 cells[J]. Eur J Immunol, 2007, 37: 3021-3029.
  • 10Forger F, Marcoli N, Gadola S, et al. Pregnancy induces numerical and functional changes of CD4^+ CD25^high regulatory T cells in patients with rheumatoid arthritis[J]. Ann Rheum Dis, 2008, 67:984-990.

共引文献8

同被引文献28

  • 1徐军发,袁春雷,杨衡,赵坤,胡国艳,龚非力.小鼠B7-H4基因克隆及真核表达载体的构建[J].细胞与分子免疫学杂志,2007,23(7):665-667. 被引量:9
  • 2Hu YL, Metz DP, Chung J, et aI.B7RP-I blockade meliorates autoim- munity through regulation of follicular helper TceUs[J].J Immunol, 2009,182:1421-1428.
  • 3Arnett FC, Edworthy SM, Bloch DA, et al. The American Rheumatism Association 1987 revised criteria for the classification of rheumatoid ar- thritis[J]. Arthritis Rheum, 1988,31 (3):315-324.
  • 4Prevoo ML,vant Hof MA ,Kuper HH,et al.Modified disease activity scores that include twenty-eight-joint counts.Development and valid- llon in a prospective longitudinal study of patients with rheumatoid ar- thrifts[J]. Arthritis Rheum, 1995,38(1):44-48.
  • 5Dehmel S, Wang S, Schmidt C, et al. Chemokine recepter Ccr5 defi- ciency induce saltemative macrophage activation and improves long-term renal, allograft outcome[J]. Eur J Immunol, 2010, 40(1) : 267-278.
  • 6Makinen H, Hannonen P, Sokka T,et al. Definitions of remission for rheumatoid arthritis and review of selected clinical cohorts and ran- domised clinical trials for the rate of remission[J]. Clin Exp Rheuma- tol, 2006,24(6):S22-28.
  • 7David L Scott,Frederick Wolfe,Tom WJ Huizinga.Rheumatoid arthritis[J].The Lancet.2010(9746)
  • 8Joaquim Polido-Pereira,Elsa Vieira-Sousa,Jo?o Eurico Fonseca.Rheumatoid arthritis: What is refractory disease and how to manage it?[J].Autoimmunity Reviews.2011(11)
  • 9Yosuke Kamimura,Hiroko Kobori,Jinhua Piao,Masaaki Hashiguchi,Koichiro Matsumoto,Sachiko Hirose,Miyuki Azuma.Possible involvement of soluble B7-H4 in T cell-mediated inflammatory immune responses[J].Biochemical and Biophysical Research Communications.2009(2)
  • 10胡国艳,郑淑华,刘伟,那志萍,肖欢,张良清,徐军发.检测可溶性B7-H4 ELISA夹心法的建立[J].细胞与分子免疫学杂志,2008,24(8):831-833. 被引量:29

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