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类风湿关节炎中的组胺

Histamine in rheumatoid arthritis.

作者信息

Adlesic M, Verdrengh M, Bokarewa M, Dahlberg L, Foster S J, Tarkowski A

机构信息

Department of Rheumatology and Inflammation Research, Göteborg University, Göteborg, Sweden.

出版信息

Scand J Immunol. 2007 Jun;65(6):530-7. doi: 10.1111/j.1365-3083.2007.01938.x.

DOI:10.1111/j.1365-3083.2007.01938.x
PMID:17523945
Abstract

Rheumatoid arthritis (RA) is an autoimmune disease characterized by a persistent inflammation of the synovium, leading to the erosion of articular cartilage and bone. Synovial mast cells and their effector molecule, histamine, receive increased attention as mediators of joint inflammation. The aim of our study was to analyse levels of free histamine in serum and joint fluid of RA patients and to evaluate the potential inflammatogenic properties of histamine in vivo and in vitro. Histamine levels were measured by an ELISA in synovial fluid and sera of RA patients and of healthy controls. Histamine levels were also assessed in plasma of RA patients undergoing anti-TNF-alpha treatment. In the murine part of the study, histamine was injected intra-articularly in the knee joint of mice and the joints were subsequently analysed with respect to induction of inflammation. RA patients displayed significantly lower levels of histamine in circulation (0.93 +/- 0.16 ng/ml) compared with the healthy controls (1.89 +/- 0.45 ng/ml, P < 0.001). Locally, in synovial fluid the levels of histamine were even lower (0.37 +/- 0.16 ng/ml, P < 0.0006). Long-term anti-TNF-alpha treatment significantly increased circulating levels of histamine in RA patients. Our experiments on animals show that histamine on its own neither induces inflammation in the joint cavity nor influences the course of HMGB1 and peptidoglycan-induced joint inflammation. Based on our experimental and clinical studies we suggest that histamine lacks harmful properties in RA.

摘要

类风湿性关节炎(RA)是一种自身免疫性疾病,其特征在于滑膜持续发炎,导致关节软骨和骨骼受到侵蚀。滑膜肥大细胞及其效应分子组胺作为关节炎症的介质受到越来越多的关注。我们研究的目的是分析类风湿性关节炎患者血清和关节液中游离组胺的水平,并评估组胺在体内和体外的潜在致炎特性。通过酶联免疫吸附测定法(ELISA)测量类风湿性关节炎患者和健康对照者的滑液和血清中的组胺水平。还对接受抗TNF-α治疗的类风湿性关节炎患者的血浆中的组胺水平进行了评估。在该研究的小鼠部分中,将组胺关节内注射到小鼠的膝关节中,随后对关节进行炎症诱导分析。与健康对照者(1.89±0.45 ng/ml,P<0.001)相比,类风湿性关节炎患者循环中的组胺水平显著降低(0.93±0.16 ng/ml)。在局部,滑液中的组胺水平甚至更低(0.37±0.16 ng/ml,P<0.0006)。长期抗TNF-α治疗显著提高了类风湿性关节炎患者循环中的组胺水平。我们的动物实验表明,组胺本身既不会在关节腔内诱导炎症,也不会影响HMGB1和肽聚糖诱导的关节炎症的进程。基于我们的实验和临床研究,我们认为组胺在类风湿性关节炎中没有有害特性。

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