Rubér M, Berg A, Ekerfelt C, Olaison G, Andersson R E
Division of Surgery, Department of Biomedicine and Surgery, Faculty of Health Sciences, Linköping University, Linköping, Sweden.
Clin Exp Immunol. 2006 Jan;143(1):117-24. doi: 10.1111/j.1365-2249.2005.02957.x.
Appendicitis is one of the most common and costly acute abdominal states of illnesses. Previous studies suggest two types of appendicitis which may be different entities, one which may resolve spontaneously and another that progresses to gangrene and perforation. Gangrenous appendicitis has a positive association to states of Th1 mediated immunity whereas Th2 associated immune states are associated with lower risk of appendicitis. This study investigated the inflammatory response pattern in patients previously appendicectomized for gangrenous (n = 7), or phlegmonous appendicitis (n = 8) and those with a non-inflamed appendix (n = 5). Peripheral blood mononuclear cells were analysed with ELISPOT analysis for number of spontaneous or antigen/mitogen stimulated IFN-gamma, IL-4, IL-10 and IL-12 secreting cells or with ELISA for concentration of spontaneous or antigen/mitogen stimulated IFN-gamma, IL-5 and IL-10. Spontaneously IL-10 secreting cells/100,000 lymphocytes were increased in the gangrenous group compared to the phlegmonous group (P = 0.015). The median concentration of IL-10 secreted after Tetanus toxoid (TT)-stimulation were higher in the gangrenous group and the control group, than the phlegmonous group (P = 0.048 and P = 0.027, respectively). The median concentration of TT induced IFN-gamma secretion was higher for the gangrenous group compared to both the phlegmonous group and the control group (P = 0.037 and P = 0.003). Individuals with a history of gangrenous appendicitis demonstrated ability to increased IL-10 and IFN-gamma production. The increased IFN-gamma may support the notion of gangrenous appendicitis as an uncontrolled Th1 mediated inflammatory response and increased IL-10 may speculatively indicate the involvement of cytotoxic cells in the progression to perforation.
阑尾炎是最常见且治疗费用高昂的急性腹部疾病之一。先前的研究表明阑尾炎有两种类型,可能是不同的病症,一种可能会自行缓解,另一种则会发展为坏疽和穿孔。坏疽性阑尾炎与Th1介导的免疫状态呈正相关,而Th2相关的免疫状态与阑尾炎风险较低有关。本研究调查了先前因坏疽性阑尾炎(n = 7)、蜂窝织炎性阑尾炎(n = 8)而接受阑尾切除术的患者以及阑尾未发炎患者(n = 5)的炎症反应模式。采用酶联免疫斑点分析(ELISPOT分析)检测外周血单个核细胞中自发或抗原/丝裂原刺激后分泌干扰素-γ、白细胞介素-4、白细胞介素-10和白细胞介素-12的细胞数量,或采用酶联免疫吸附测定(ELISA)检测自发或抗原/丝裂原刺激后干扰素-γ、白细胞介素-5和白细胞介素-10的浓度。与蜂窝织炎性阑尾炎组相比,坏疽性阑尾炎组中自发分泌白细胞介素-10的细胞/100,000淋巴细胞数量增加(P = 0.015)。破伤风类毒素(TT)刺激后分泌的白细胞介素-10的中位浓度在坏疽性阑尾炎组和对照组中均高于蜂窝织炎性阑尾炎组(分别为P = 0.048和P = 0.027)。与蜂窝织炎性阑尾炎组和对照组相比,坏疽性阑尾炎组中TT诱导的干扰素-γ分泌的中位浓度更高(P = 0.037和P = 0.003)。有坏疽性阑尾炎病史的个体表现出白细胞介素-10和干扰素-γ产生增加的能力。干扰素-γ增加可能支持坏疽性阑尾炎是一种不受控制的Th1介导的炎症反应这一观点,而白细胞介素-10增加可能推测性地表明细胞毒性细胞参与了穿孔的进展过程。