Stagg A J, Hughes R A, Keat A C, Elsley W A, Knight S C
Imperial College School of Medicine, Northwick Park Institute for Medical Research, Harrow.
Br J Rheumatol. 1996 Nov;35(11):1082-90. doi: 10.1093/rheumatology/35.11.1082.
T cells and antigen-presenting cells (APC) accumulate in the joint in reactive arthritis and there are reports that the T cells are a population selected for responsiveness to the causative agent. In this work, the latter view is questioned by detailed studies of the antigen specificities of the lymphocytes within the joint (SFMC) and peripheral blood (PBMC) of patients with reactive arthritis triggered by infection with Chlamydia trachomatis. Using a hanging-drop microculture system. SFMC displayed enhanced responses not only to antigens from the triggering organism, but also to other antigens, including PPD and tetanus toxoid, to which the patients were likely to have had prior exposure. No evidence was obtained for a dominant cross-reactive T-cell response to epitopes common to these antigen preparations, confirming the polyclonal nature of the infiltrate. In contrast to the broad specificity of the T-cell infiltrate, two experimental approaches indicated that APC within the joint carried chlamydial antigen. The failure of antigen-bearing APC to interact with T cells at this site may underlie the inability to clear microbial antigen from the joint.
T细胞和抗原呈递细胞(APC)在反应性关节炎患者的关节中积聚,并且有报道称T细胞是针对病原体具有反应性的特定细胞群体。在这项研究中,沙眼衣原体感染引发的反应性关节炎患者关节内(滑膜成纤维细胞,SFMC)和外周血(外周血单核细胞,PBMC)淋巴细胞抗原特异性的详细研究对后一种观点提出了质疑。使用悬滴微培养系统,SFMC不仅对引发病原体的抗原,而且对患者可能先前接触过的其他抗原(包括PPD和破伤风类毒素)表现出增强的反应。未获得对这些抗原制剂共有的表位产生显性交叉反应性T细胞应答的证据,证实了浸润的多克隆性质。与T细胞浸润的广泛特异性相反,两种实验方法表明关节内的APC携带衣原体抗原。携带抗原的APC在此部位无法与T细胞相互作用,可能是关节中无法清除微生物抗原的原因。