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类风湿关节炎、脊柱关节病、骨关节炎患者及正常患者滑膜组织中核因子κB受体活化因子配体(RANKL)的表达:半定量和定量分析

Receptor activator NF-kappaB ligand (RANKL) expression in synovial tissue from patients with rheumatoid arthritis, spondyloarthropathy, osteoarthritis, and from normal patients: semiquantitative and quantitative analysis.

作者信息

Crotti T N, Smith M D, Weedon H, Ahern M J, Findlay D M, Kraan M, Tak P P, Haynes D R

机构信息

Department of Pathology, University of Adelaide, Adelaide, South Australia.

出版信息

Ann Rheum Dis. 2002 Dec;61(12):1047-54. doi: 10.1136/ard.61.12.1047.

DOI:10.1136/ard.61.12.1047
PMID:12429533
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1753975/
Abstract

OBJECTIVES

To compare receptor activator of NF-kappaB ligand (RANKL) production in the synovial tissue from patients with active rheumatoid arthritis (RA), inactive RA, spondyloarthropathies (SpA), osteoarthritis, and from normal subjects. In addition, to establish the cell lineages expressing RANKL in these tissues.

METHODS

Immunohistological analysis of frozen synovial tissue biopsy specimens was performed using a monoclonal antibody (mAb) to detect RANKL. Sections were evaluated by computer assisted image analysis and semiquantitative analysis to compare RANKL expression between groups. Dual and sequential labelling with mAb RANKL and cell lineage specific monoclonal antibodies were used to determine the types of cells expressing RANKL.

RESULTS

Higher levels of RANKL were expressed in tissues from patients with active RA and SpA than in tissues from patients with inactive RA, osteoarthritis, and from normal subjects. RANKL protein was associated with CD3 antigen-positive lymphocytes and some macrophages. RANKL was predominantly associated with activated, memory T cells (CD45Ro positive cells) in patients with active RA and spondyloarthropathy (SpA).

CONCLUSIONS

The highest levels of RANKL were detected in patients with RA with active synovitis and in some patients with SpA. An increase in RANKL in the inflamed joint of patients with RA, produced by infiltrating activated T cells and macrophages, is likely to be an important cause of joint erosions in RA.

摘要

目的

比较活动性类风湿关节炎(RA)、非活动性RA、脊柱关节病(SpA)、骨关节炎患者及正常受试者滑膜组织中核因子κB受体活化因子配体(RANKL)的产生情况。此外,确定这些组织中表达RANKL的细胞谱系。

方法

使用单克隆抗体(mAb)对冷冻滑膜组织活检标本进行免疫组织学分析以检测RANKL。通过计算机辅助图像分析和半定量分析对切片进行评估,以比较各组间RANKL的表达情况。使用RANKL单克隆抗体和细胞谱系特异性单克隆抗体进行双重和连续标记,以确定表达RANKL的细胞类型。

结果

活动性RA和SpA患者组织中RANKL的表达水平高于非活动性RA、骨关节炎患者组织及正常受试者组织。RANKL蛋白与CD3抗原阳性淋巴细胞及部分巨噬细胞相关。在活动性RA和脊柱关节病(SpA)患者中,RANKL主要与活化的记忆T细胞(CD45Ro阳性细胞)相关。

结论

在伴有活动性滑膜炎的RA患者及部分SpA患者中检测到最高水平的RANKL。RA患者炎症关节中由浸润的活化T细胞和巨噬细胞产生的RANKL增加,可能是RA关节侵蚀的重要原因。

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Osteoprotegerin and receptor activator of nuclear factor kappaB ligand (RANKL) regulate osteoclast formation by cells in the human rheumatoid arthritic joint.骨保护素和核因子κB受体激活剂配体(RANKL)调节人类类风湿性关节炎关节中细胞的破骨细胞形成。
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