Beaman M H, Hunter C A, Remington J S
Department of Immunology and Infectious Diseases, Palo Alto Medical Foundation, 94301.
J Immunol. 1994 Nov 15;153(10):4583-7.
Toxoplasma gondii is a major pathogen of immunocompromised hosts, and one defense mechanism against the parasite is activation of macrophages (M phi) for toxoplasmacidal activity by IFN-gamma after triggering by TNF-alpha. IL-6, IFN-gamma, and TNF-alpha are cytokines involved in inflammatory responses and are induced by T. gondii infection. We studied the interaction of these three cytokines using an in vitro model of T. gondii infection. Pretreatment (but not post-treatment) of unelicited murine peritoneal M phi with IL-6 enhanced T. gondii replication in a dose-dependent manner. Pretreatment with IFN-gamma resulted in active killing of parasites whereas the addition of IL-6 to IFN-gamma pretreatment resulted in a reversal of IFN-gamma-mediated toxoplasmacidal activity. Combining TNF-alpha with IL-6 and IFN-gamma pretreatment resulted in restoration of toxoplasmacidal activity. Addition of a polyclonal anti-TNF-alpha Ab to IL-6 and IFN-gamma pretreatment resulted in enhancement in the IL-6-mediated impairment of IFN-gamma function. These data taken together suggest that IL-6 enhances intracellular replication of T. gondii and reverses IFN-gamma mediated activation of murine peritoneal M phi, and that certain of the interactions between these two cytokines may be at the level of TNF-alpha triggering.
刚地弓形虫是免疫功能低下宿主的主要病原体,针对该寄生虫的一种防御机制是在肿瘤坏死因子-α(TNF-α)触发后,通过γ干扰素(IFN-γ)激活巨噬细胞(Mφ)以产生杀弓形虫活性。白细胞介素-6(IL-6)、IFN-γ和TNF-α是参与炎症反应的细胞因子,由刚地弓形虫感染诱导产生。我们使用刚地弓形虫感染的体外模型研究了这三种细胞因子之间的相互作用。用IL-6对未引发的小鼠腹腔Mφ进行预处理(而非后处理)以剂量依赖的方式增强了刚地弓形虫的复制。用IFN-γ预处理导致寄生虫被有效杀伤,而在IFN-γ预处理中加入IL-6则导致IFN-γ介导的杀弓形虫活性逆转。将TNF-α与IL-6和IFN-γ预处理相结合导致杀弓形虫活性恢复。向IL-6和IFN-γ预处理中加入多克隆抗TNF-α抗体导致IL-6介导的IFN-γ功能损害增强。综合这些数据表明,IL-6增强了刚地弓形虫的细胞内复制并逆转了IFN-γ介导的小鼠腹腔Mφ激活,并且这两种细胞因子之间的某些相互作用可能发生在TNF-α触发水平。