摘要
目的:了解类风湿关节炎(RA)血清、滑液和滑膜组织中转化生长因β1(TGFβ1)、细胞间粘附分子1(ICAM1)及细胞间粘附分子3(ICAM3)的变化。方法:采用ELISA及ABC免疫组化方法检测RA患者血清、滑液和滑膜中TGFβ1、ICAM1和ICAM3的浓度和阳性程度。结果:RA血清中TGFβ1含量较低,而ICAM1含量明显升高,ICAM3含量正常,滑液中ICAM3含量低于血清含量。RA血清中TGFβ1含量与ICAM1含量呈中度负相关,与ICAM3含量无显著相关。在RA滑膜中巨噬细胞、滑膜衬里细胞和成纤维细胞TGFβ1染色阳性,巨噬细胞、滑膜衬里细胞、成纤维细胞和血管内皮细胞ICAM1染色阳性。结论:TGFβ1和ICAM1参与了RA的发生和发展过程,在RA慢性炎症中,ICAM1对炎细胞转移并聚集于滑膜可能有重要作用,RA外周血TGFβ1浓度减低伴随ICAM1浓度的增加。
Objective:To explore the change of transforming growth factorβ1 or intracellular adhession molecule in sera,synovial fluid and synovial tissue in patients with rheumatoid arthritis.Methods:The expression of TGFβ1,ICAM1 and ICAM3 in sera,synovial fluid or synovial tissue in patients with RA was measured or stained using ELISA method and avidinbiotinperooxidase technique.Results:The contents of serum TGFβ1 in patients with RA were lower than those in normal subjects.But the contents of serum ICAM1 in patients with RA were higher.The contents of serum ICAM3 in RA were similar to those of ICAM3 in normal subjects,but the contents of ICAM3 in the synovial fluid in patients with RA were lower than the contents of ICAM3 in the sera in patients with RA.The contents of serum TGFβ1 in patients with RA were negatively correlated with the contents of serum ICAM1 in patients with RA.Positive staining for TGFβ1 was found on macrophage,fibroblast and synovial lining cell in rheumatoid synovium.The staining of lymphocyte and endotheliocyte was negative in rheumatoid synovium.The staining of ICAM1 was positive on macrophage,synovial lining cell,fibroblast and endotheliocyte in rheumatiod synovium.Conclusion:TGFβ1 and ICAM1 take part in the occurrence or development course of RA.ICAM1 plays an important role in inflammatory cell transforming and aggregating to synovial tissue.The higher the contents of serum TGFβ1 in the patients with RA,the lower the contents of the sreum ICAM1.
出处
《中华风湿病学杂志》
CAS
CSCD
1998年第1期21-24,共4页
Chinese Journal of Rheumatology
关键词
类风湿性关节炎
转化生长因子Β
细胞粘附分子
transforming growth factorβ1 intracellular adhesion molecule1 intracellular adhesion molecule3 arthritis,rheumatoid