Kita Masakazu
Department of Microbiology, Kyoto Prefectural University of Medicine.
Nihon Rinsho. 2006 Jul;64(7):1269-74.
IFN-gamma is induced by receptor-mediated stimulation or in response to early produced cytokines, including interleukin-12 (IL-12), IL-18, and IFN-alpha/beta, or by stimulation through T cell receptors (TCRs) or natural killer (NK) cell receptors. Cellular effects of IFN-gamma are described, including up-regulation of pathogen recognition, antigen processing and presentation, the antiviral state, inhibition of cellular proliferation and effects on apoptosis, activation of microbicidal effector functions, immunomodulation, and leukocyte trafficking. Innate production of IFN-gamma is a critical step in immunological defense against certain pathogen, such as intracellular bacteria, viruses and fungi. This review focuses on recent progress of the role of IFN-gamma in nonviral infections.
γ-干扰素可通过受体介导的刺激诱导产生,或对早期产生的细胞因子(包括白细胞介素-12(IL-12)、IL-18和α/β干扰素)作出反应而产生,也可通过T细胞受体(TCR)或自然杀伤(NK)细胞受体的刺激产生。文中描述了γ-干扰素的细胞效应,包括病原体识别上调、抗原加工和呈递、抗病毒状态、细胞增殖抑制及对细胞凋亡的影响、杀菌效应功能激活、免疫调节和白细胞迁移。γ-干扰素的天然产生是针对某些病原体(如细胞内细菌、病毒和真菌)进行免疫防御的关键步骤。本综述重点关注γ-干扰素在非病毒感染中作用的最新进展。