Department of Public Health and Infectious Diseases, Pasteur Institute Cenci Bolognetti Foundation, Sapienza University of Rome, Rome, Italy.
San Raffaele Pisana, IRCCS, Telematic University, Rome, Italy.
Front Immunol. 2018 Jul 30;9:1747. doi: 10.3389/fimmu.2018.01747. eCollection 2018.
Influenza virus replicates intracellularly exploiting several pathways involved in the regulation of host responses. The outcome and the severity of the infection are thus strongly conditioned by multiple host factors, including age, sex, metabolic, and redox conditions of the target cells. Hormones are also important determinants of host immune responses to influenza and are recently proposed in the prophylaxis and treatment. This study shows that female mice are less susceptible than males to mouse-adapted influenza virus (A/PR8/H1N1). Compared with males, PR8-infected females display higher survival rate (+36%), milder clinical disease, and less weight loss. They also have milder histopathological signs, especially free alveolar area is higher than that in males, even if pro-inflammatory cytokine production shows slight differences between sexes; hormone levels, moreover, do not vary significantly with infection in our model. Importantly, viral loads (both in terms of viral M1 RNA copies and tissue culture infectious dose 50%) are lower in PR8-infected females. An analysis of the mechanisms contributing to sex disparities observed during infection reveals that the female animals have higher total antioxidant power in serum and their lungs are characterized by increase in (i) the content and biosynthesis of glutathione, (ii) the expression and activity of antioxidant enzymes (peroxiredoxin 1, catalase, and glutathione peroxidase), and (iii) the expression of the anti-apoptotic protein Bcl-2. By contrast, infected males are characterized by high expression of NADPH oxidase 4 oxidase and phosphorylation of p38 MAPK, both enzymes promoting viral replication. All these factors are critical for cell homeostasis and susceptibility to infection. Reappraisal of the importance of the host cell redox state and sex-related effects may be useful in the attempt to develop more tailored therapeutic interventions in the fight against influenza.
流感病毒在细胞内复制,利用多种参与宿主反应调节的途径。因此,感染的结果和严重程度受到多种宿主因素的强烈影响,包括年龄、性别、靶细胞的代谢和氧化还原状态。激素也是宿主对流感免疫反应的重要决定因素,最近也被提出用于预防和治疗。本研究表明,雌性小鼠比雄性小鼠对适应小鼠的流感病毒(A/PR8/H1N1)的易感性更低。与雄性相比,感染 PR8 的雌性具有更高的存活率(+36%)、较轻的临床疾病和较少的体重减轻。它们的组织病理学迹象也较轻,特别是游离肺泡面积高于雄性,即使性别之间的促炎细胞因子产生略有差异;此外,在我们的模型中,激素水平在感染时没有明显变化。重要的是,PR8 感染雌性小鼠的病毒载量(无论是 M1 RNA 拷贝数还是组织培养感染剂量 50%)均较低。对感染过程中观察到的性别差异的机制分析表明,雌性动物的血清总抗氧化能力较高,其肺部表现为:(i)谷胱甘肽的含量和生物合成增加,(ii)抗氧化酶(过氧化物酶 1、过氧化氢酶和谷胱甘肽过氧化物酶)的表达和活性增加,以及(iii)抗凋亡蛋白 Bcl-2 的表达增加。相比之下,感染的雄性动物以 NADPH 氧化酶 4 氧化酶和 p38 MAPK 的磷酸化高表达为特征,这两种酶均促进病毒复制。所有这些因素对细胞内稳态和感染易感性都至关重要。重新评估宿主细胞氧化还原状态和性别相关影响的重要性,可能有助于尝试开发更针对流感的治疗干预措施。