Infections Associated with Iron Administration.

Manfred Nairz, Guenter Weiss
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引用次数: 5

Abstract

A dynamic interplay between the host and pathogen determines the course and outcome of infections. A central venue of this interplay is the struggle for iron, a micronutrient essential to both the mammalian host and virtually all microbes. The induction of the ironregulatory hormone hepcidin is an integral part of the acute phase response. Hepcidin switches off cellular iron export via ferroportin-1 and sequesters the metal mainly within macrophages, which limits the transfer of iron to the serum to restrict its availability for extracellular microbes. When intracellular microbes are present within macrophages though, the opposite regulation is initiated because infected cells respond with increased ferroportin-1 expression and enhanced iron export as a strategy of iron withdrawal from engulfed bacteria. Given these opposing regulations, it is not surprising that disturbances of mammalian iron homeostasis, be they attributable to genetic alterations, hematologic conditions, dietary iron deficiency or unconsidered iron supplementation, may affect the risk and course of infections. Therefore, acute, chronic or latent infections need to be adequately controlled by antimicrobial therapy before iron is administered to correct deficiency. Iron deficiency per se may negatively affect growth and development of children as well as cardiovascular performance and quality of life of patients. Of note, mild iron deficiency in regions with a high endemic burden of infections is associated with a reduced prevalence and a milder course of certain infections which may be traced back to effects of iron on innate and adaptive immune function as well as to restriction of iron for pathogens. Finally, absolute and functional causes of iron deficiency need to be differentiated, because in the latter form, oral iron supplementation is inefficient and intravenous application may adversely affect the course of the underlying disease such as a chronic infection. This chapter summarizes our current knowledge on the regulation of iron metabolism and the interactions between iron and the immune response against microbes. Moreover, some of the unanswered questions on the association of iron administration and infections are addressed.

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与服用铁剂有关的感染。
宿主和病原体之间的动态相互作用决定了感染的过程和结果。这种相互作用的中心场所是对铁的争夺,铁是一种对哺乳动物宿主和几乎所有微生物都必不可少的微量营养素。铁调节激素hepcidin的诱导是急性期反应的一个组成部分。Hepcidin通过铁转运蛋白-1关闭细胞铁输出,并将金属主要隔离在巨噬细胞内,这限制了铁向血清的转移,从而限制了其对细胞外微生物的利用。然而,当细胞内微生物存在于巨噬细胞中时,相反的调控被启动,因为受感染的细胞以增加铁转运蛋白-1表达和增强铁输出作为从被吞噬的细菌中提取铁的策略。鉴于这些相反的规律,哺乳动物铁稳态的紊乱,无论是由于遗传改变、血液学状况、饮食铁缺乏还是未考虑的铁补充,都可能影响感染的风险和过程,这并不奇怪。因此,急性、慢性或潜伏性感染需要通过抗菌治疗得到充分控制,然后再给铁以纠正缺乏症。缺铁本身会对儿童的生长发育、心血管功能和患者的生活质量产生负面影响。值得注意的是,在地方性感染负担高的地区,轻度缺铁与某些感染的患病率降低和病程较轻有关,这可追溯到铁对先天和适应性免疫功能的影响,以及对病原体的铁限制。最后,需要区分铁缺乏的绝对原因和功能性原因,因为在后一种情况下,口服补铁效率低下,静脉注射铁可能对潜在疾病(如慢性感染)的病程产生不利影响。本章总结了我们目前对铁代谢的调控以及铁与微生物免疫反应之间的相互作用的了解。此外,一些未解决的问题,铁的管理和感染的关系是解决。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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