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类风湿关节炎患者多个部位滑膜中免疫活性细胞的特征

Characteristics of immunocompetent cells in synovial membranes from multiple sites in patients with rheumatoid arthritis.

作者信息

Hanly J G, Pledger D

机构信息

Department of Medicine, Victoria General Hospital, Nova Scotia, Canada.

出版信息

Ann Rheum Dis. 1992 Sep;51(9):1066-8. doi: 10.1136/ard.51.9.1066.

DOI:10.1136/ard.51.9.1066
PMID:1384441
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1004839/
Abstract

The phenotypic characterization of enzymatically dissociated mononuclear cells in synovial membrane samples from multiple sites in two patients with rheumatoid arthritis (RA) were examined by fluorescence activated flow cytometry. In synovial membrane samples from each patient there was a consistent increase in the proportion of CD8+ cells (suppressor/cytotoxic), CD14+ cells (monocytes/macrophages), and HLA-DR+ cells compared with paired peripheral blood mononuclear cells. The proportion of CD4+ cells (helper/inducer) in synovial membrane was variable. Studies of in vitro production of IgM and IgM rheumatoid factor in one patient showed strikingly similar values for synovial membrane rheumatoid factor production at the two sites, which was enhanced compared with production in peripheral blood. These results suggest that in individual patients with RA the intra-articular immune response is comparable at multiple anatomical sites and that it is distinct from that in peripheral blood.

摘要

通过荧光激活流式细胞术对两名类风湿性关节炎(RA)患者多个部位滑膜膜样本中酶解单核细胞的表型特征进行了检测。与配对的外周血单核细胞相比,每名患者滑膜膜样本中CD8 +细胞(抑制/细胞毒性)、CD14 +细胞(单核细胞/巨噬细胞)和HLA-DR +细胞的比例持续增加。滑膜膜中CD4 +细胞(辅助/诱导)的比例各不相同。对一名患者体外产生IgM和IgM类风湿因子的研究表明,两个部位滑膜膜类风湿因子的产生值极为相似,与外周血中的产生相比有所增强。这些结果表明,在个体RA患者中,关节内免疫反应在多个解剖部位具有可比性,且与外周血中的免疫反应不同。

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Clin Rheumatol. 1995 Jan;14(1):43-50. doi: 10.1007/BF02208083.
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Measurement of colony-stimulating factors in synovial fluid: potential clinical value.滑膜液中集落刺激因子的测定:潜在临床价值。
Rheumatol Int. 1995;14(5):177-82. doi: 10.1007/BF00262295.

本文引用的文献

1
In situ localization of lymphocyte subsets in synovial membranes of patients with rheumatoid arthritis with monoclonal antibodies.用单克隆抗体对类风湿关节炎患者滑膜中淋巴细胞亚群进行原位定位。
J Rheumatol. 1982 May-Jun;9(3):359-65.
2
Synovial fluid lymphocytes differ from peripheral blood lymphocytes in patients with rheumatoid arthritis.类风湿性关节炎患者的滑液淋巴细胞与外周血淋巴细胞不同。
J Immunol. 1982 Jan;128(1):351-4.
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An immunohistological analysis of lymphocyte subpopulations and their microenvironment in the synovial membranes of patients with rheumatoid arthritis using monoclonal antibodies.运用单克隆抗体对类风湿性关节炎患者滑膜中的淋巴细胞亚群及其微环境进行免疫组织学分析。
Clin Exp Immunol. 1982 Jul;49(1):22-30.
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T-cell subpopulations in the peripheral blood of patients with connective tissue diseases as determined by flow cytometry using monoclonal antibodies.使用单克隆抗体通过流式细胞术测定结缔组织病患者外周血中的T细胞亚群。
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Lymphocyte subsets and inflammatory indices in synovial fluid and blood of patients with rheumatoid arthritis.类风湿关节炎患者滑液和血液中的淋巴细胞亚群及炎症指标
J Rheumatol. 1984 Dec;11(6):754-9.
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Immune function in severe, active rheumatoid arthritis. A relationship between peripheral blood mononuclear cell proliferation to soluble antigens and synovial tissue immunohistologic characteristics.重度活动期类风湿关节炎的免疫功能。外周血单个核细胞对可溶性抗原的增殖与滑膜组织免疫组织学特征之间的关系。
J Clin Invest. 1984 Oct;74(4):1173-85. doi: 10.1172/JCI111526.
7
Immunoelectron microscopic study of the distribution of T cell subsets in rheumatoid synovium.类风湿性滑膜中T细胞亚群分布的免疫电子显微镜研究
J Exp Med. 1983 Oct 1;158(4):1191-210. doi: 10.1084/jem.158.4.1191.
8
Analysis of T cell subsets in the peripheral blood and synovial fluid of patients with rheumatoid arthritis by means of monoclonal antibodies.利用单克隆抗体对类风湿关节炎患者外周血和滑液中的T细胞亚群进行分析。
Ann Rheum Dis. 1983 Aug;42(4):357-61. doi: 10.1136/ard.42.4.357.
9
Functional analysis of human T cell subsets defined by monoclonal antibodies. VI. Distinct and opposing immunoregulatory functions within the OKT8+ population.由单克隆抗体定义的人T细胞亚群的功能分析。VI. OKT8+群体内不同且相反的免疫调节功能。
J Mol Cell Immunol. 1984;1(2):103-13.
10
Rheumatoid arthritis: a disease of T-lymphocyte/macrophage immunoregulation.类风湿性关节炎:一种T淋巴细胞/巨噬细胞免疫调节疾病。
Lancet. 1981 Oct 17;2(8251):839-42. doi: 10.1016/s0140-6736(81)91107-7.