Collins Helen L
Department of Infectious Disease, Division of Immunology, Infection and Inflammatory Disease, Kings College London, London, UK.
Eur J Immunol. 2008 Jul;38(7):1803-6. doi: 10.1002/eji.200838505.
During infection one critical host defence strategy is an attempt to withhold iron from invading pathogens. This is achieved by by proinflammatory cytokines such as IL-6 inducing hepcidin. The net result of this is the removal of iron from the circulation and its sequestration within cells, including cells of the immune system such as macrophages. As macrophages are central cells for controlling infections with intracellular bacteria such as Salmonella and Mycobacteria, modulation of iron by hepcidin can lead to the provision of an ideal cellular iron source for these pathogens. Here we discuss how activation of macrophages with IFN-gamma not only up-regulates antimicrobial effector mechanisms but also modulates iron regulatory proteins such as ferroportin to reduce intracellular iron availability.
在感染期间,一种关键的宿主防御策略是试图阻止铁进入入侵的病原体。这是通过促炎细胞因子如白细胞介素-6诱导铁调素来实现的。其最终结果是铁从循环中被清除并在细胞内被隔离,包括免疫系统的细胞如巨噬细胞。由于巨噬细胞是控制细胞内细菌如沙门氏菌和分枝杆菌感染的核心细胞,铁调素对铁的调节可导致为这些病原体提供理想的细胞铁源。在此我们讨论用γ干扰素激活巨噬细胞不仅上调抗菌效应机制,还调节铁调节蛋白如铁转运蛋白以降低细胞内铁的可用性。