Müssener A, Litton M J, Lindroos E, Klareskog L
Department of Rheumatology, Karolinska Hospital, Stockholm, Sweden.
Clin Exp Immunol. 1997 Mar;107(3):485-93. doi: 10.1046/j.1365-2249.1997.3181214.x.
The kinetics of cytokine production in arthritic limbs of mice with CIA was determined by using modified immunohistochemical techniques. Tissue cryostat sections of undecalcified whole paws were analysed for the presence of tumour necrosis factor-alpha (TNF-alpha), IL-6, IL-2, IL-4, IL-5 interferon-gamma (IFN-gamma), transforming growth factor-beta 2 (TGF-beta2) and TGF-beta3. Locally produced TNF-alpha, IL-6 and TGF-beta2 were observed within the lining layer, sublining and pannus at all stages of disease. The staining of TNF-alpha was particularly intense at the cartilage-pannus junction. In contrast to the monokines, IFN-gamma and TGF-beta3 were only expressed in scattered cells within the deeper layers of the synovia. Interestingly, IFN-gamma was not present in the late phase of CIA, despite the continued presence of TNF-alpha and IL-6 in the pannus. Production of IL-2, IL-4 or IL-5 was not detected in any joint. The observed pattern of a relative paucity of T cell-derived cytokines and an abundance of monokines during the late phase of T cell-dependent CIA indicates that the synovial cytokine pattern previously described in rheumatoid arthritis (RA) is fully compatible with a pathogenic role of T cells. The temporal as well as spatial dissociation between expression of T cell-derived cytokines and monokines indicates that T cell-independent mechanisms may also be of importance in the triggering of monokine production during arthritis.
采用改良的免疫组织化学技术测定了胶原诱导性关节炎(CIA)小鼠关节炎肢体中细胞因子产生的动力学。对未脱钙全爪的组织冰冻切片进行分析,检测肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)、白细胞介素-2(IL-2)、白细胞介素-4(IL-4)、白细胞介素-5、干扰素-γ(IFN-γ)、转化生长因子-β2(TGF-β2)和转化生长因子-β3(TGF-β3)的存在情况。在疾病的各个阶段,在内衬层、衬里下层和血管翳中均观察到局部产生的TNF-α、IL-6和TGF-β2。TNF-α在软骨-血管翳交界处的染色尤为强烈。与单核因子不同,IFN-γ和TGF-β3仅在滑膜深层的散在细胞中表达。有趣的是,尽管血管翳中持续存在TNF-α和IL-6,但在CIA的后期未检测到IFN-γ。在任何关节中均未检测到IL-2、IL-4或IL-5的产生。在T细胞依赖性CIA后期观察到的T细胞衍生细胞因子相对缺乏和单核因子丰富的模式表明,先前在类风湿关节炎(RA)中描述的滑膜细胞因子模式与T细胞的致病作用完全相符。T细胞衍生细胞因子和单核因子表达之间的时间以及空间解离表明,T细胞非依赖性机制在关节炎期间单核因子产生的触发中可能也很重要。