Deml Ludwig, Aigner Michael, Decker Jochen, Eckhardt Alexander, Schütz Christian, Mittl Peer R E, Barabas Sascha, Denk Stefanie, Knoll Gertrud, Lehn Norbert, Schneider-Brachert Wulf
Institute for Medical Microbiology and Hygiene, University of Regensburg, Franz-Josef-Strauss-Allee 11, D-93053 Regensburg, Germany.
Infect Immun. 2005 Aug;73(8):4732-42. doi: 10.1128/IAI.73.8.4732-4742.2005.
Predominant T-helper 1 (Th1) responses with increased gamma interferon (IFN-gamma) levels have been proposed to play an important role in Helicobacter pylori-induced gastritis and peptic ulceration. However, bacterial factors contributing to the initiation of Th1 polarization of H. pylori-specific immune responses have not been characterized in detail thus far. We report here on the identification of Helicobacter cysteine-rich protein A (HcpA) as a novel proinflammatory and Th1-promoting protein. The capacity of HcpA to induce immune activation was studied in splenocyte cultures of naive H. pylori-negative mice. HcpA stimulated the release of high concentrations of the proinflammatory and Th1-promoting cytokines interleukin-6 (IL-6) and IFN-gamma, in addition to significant levels of IL-12, tumor necrosis factor alpha, and IL-10. The observed cytokine profile was comparable to that induced by lipopolysaccharide but differed in the kinetics and maximum levels of cytokine production. In addition, HcpA-induced cytokine release resembled that observed upon incubation with H. pylori except for IL-10, which was only moderately released upon HcpA stimulation. Both HcpA- and H. pylori-mediated IFN-gamma production was drastically reduced by a neutralizing antibody against IL-12 but not by an anti-IL-2 antibody. Thus, HcpA seems to represent a novel bacterial virulence factor triggering the release of a concerted set of cytokines to instruct the adaptive immune system for the initiation of proinflammatory and Th1-biased immunity.
γ干扰素(IFN-γ)水平升高的主要辅助性T细胞1(Th1)反应被认为在幽门螺杆菌诱导的胃炎和消化性溃疡中起重要作用。然而,迄今为止,导致幽门螺杆菌特异性免疫反应Th1极化启动的细菌因素尚未得到详细描述。我们在此报告鉴定出富含半胱氨酸的幽门螺杆菌蛋白A(HcpA)是一种新型促炎和促进Th1的蛋白。在未感染幽门螺杆菌的小鼠脾细胞培养物中研究了HcpA诱导免疫激活的能力。HcpA刺激释放高浓度的促炎和促进Th1的细胞因子白细胞介素-6(IL-6)和IFN-γ,此外还有显著水平的IL-12、肿瘤坏死因子α和IL-10。观察到的细胞因子谱与脂多糖诱导的谱相当,但在细胞因子产生的动力学和最大水平上有所不同。此外,HcpA诱导的细胞因子释放与用幽门螺杆菌孵育时观察到的相似,但IL-10除外,IL-10在HcpA刺激下仅适度释放。抗IL-12中和抗体可显著降低HcpA和幽门螺杆菌介导的IFN-γ产生,但抗IL-2抗体则无此作用。因此,HcpA似乎代表一种新型细菌毒力因子,可触发一系列协同细胞因子的释放,以指导适应性免疫系统启动促炎和偏向Th1的免疫反应。