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Modulation of Inflammation and Immune Responses by Heme Oxygenase-1: Implications for Infection with Intracellular Pathogens

机译:血红素氧酶-1的炎症和免疫应答的调节:对细胞内病原体感染的影响

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摘要

Heme oxygenase-1 (HO-1) catalyzes the degradation of heme molecules releasing equimolar amounts of biliverdin, iron and carbon monoxide. Its expression is induced in response to stress signals such as reactive oxygen species and inflammatory mediators with antioxidant, anti-inflammatory and immunosuppressive consequences for the host. Interestingly, several intracellular pathogens responsible for major human diseases have been shown to be powerful inducers of HO-1 expression in both host cells and in vivo. Studies have shown that this HO-1 response can be either host detrimental by impairing pathogen control or host beneficial by limiting infection induced inflammation and tissue pathology. These properties make HO-1 an attractive target for host-directed therapy (HDT) of the diseases in question, many of which have been difficult to control using conventional antibiotic approaches. Here we review the mechanisms by which HO-1 expression is induced and how the enzyme regulates inflammatory and immune responses during infection with a number of different intracellular bacterial and protozoan pathogens highlighting mechanistic commonalities and differences with the goal of identifying targets for disease intervention.
机译:血红素氧合酶-1(HO-1)催化血红素分子的降解释放等摩尔量的胆汁,铁和一氧化碳。其表达响应于应力信号,例如具有抗氧化剂,抗炎和宿主免疫抑制后果的反应性氧物质和炎症介质。有趣的是,有几种负责主要人类疾病的细胞内病原体已被证明是宿主细胞和体内HO-1表达的强大诱导剂。研究表明,通过限制感染诱导的炎症和组织病理,该HO-1反应可以是通过损害病原体控制或有益的宿主而受益。这些性质使HO-1成为有问题的宿主定向治疗(HDT)的有吸引力的靶标,其中许多难以使用常规抗生素方法控制。在这里,我们审查了诱导HO-1表达的机制以及酶在感染过程中如何调节炎症和免疫应答,其中一些不同的细胞内细菌和原生动物病原体突出了机制共性和差异,以确定疾病干预目标的目标。

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