First Department of Critical Care Medicine & Pulmonary Services, Evangelismos General Hospital, National and Kapodistrian University of Athens, Athens, Greece; European Society of Clinical Microbiology and Infectious Diseases (ESCMID) Study Group for Respiratory Viruses (ESGREV), Basel, Switzerland.
European Society of Clinical Microbiology and Infectious Diseases (ESCMID) Study Group for Respiratory Viruses (ESGREV), Basel, Switzerland; Fourth Department of Internal Medicine, Attikon University Hospital, National and Kapodistrian University of Athens, Athens, Greece.
Clin Microbiol Infect. 2022 Oct;28(10):1328-1334. doi: 10.1016/j.cmi.2022.03.010. Epub 2022 Mar 17.
Respiratory viruses are associated with significant global morbidity and mortality, as well as socioeconomic factors. Certain conditions and patient groups are more susceptible to develop severe viral respiratory tract infections (RTIs).
To summarise the data on deregulated immune pathways that have been associated with increased susceptibility to severe viral RTIs in certain populations. We also describe the commonalities of the defective immune pathways across these susceptible populations that may represent possible targets for future therapeutic or preventative approaches.
We conducted free searches in Medline, Scopus, and Google Scholar for studies focusing on potential mechanisms of immune dysfunction that may be associated with severe viral RTIs in susceptible populations with conditions including pregnancy, obesity, diabetes mellitus, hypertension, cardiovascular disease, asthma, chronic obstructive pulmonary disease (COPD), chronic kidney disease, and extremes of age. We considered preclinical/animal data, original human studies, and reviews.
Innate and adaptive immune responses become quantitatively and qualitatively compromised in aging, obesity, and diabetes mellitus, with the most pronounced changes affecting T cells. Moreover, immune dysregulation by the so-called inflamm-aging results in chronic low-grade inflammation in such conditions. Increased leptin levels affect the immune system particularly in obesity, while leptin dysregulation plays a role in asthma and COPD pathogenesis. Deficient production of interferon (IFN) type I and III in response to rhinovirus contributes to asthma exacerbations. Similar attenuation of IFN production in response to influenza and rhinovirus has been documented in pregnancy. Dampened type I IFN responses have also been found in diet-induced obese mice and in obese individuals.
Immunosenescence and chronic low-grade inflammation accompanying aging and a variety of chronic conditions, such as diabetes, obesity, asthma, COPD, chronic renal disease, and hypertension, contribute to the poor outcomes observed following viral respiratory infections. Commonly affected pathways may represent potential future therapeutic targets.
呼吸道病毒与重大的全球发病率和死亡率以及社会经济因素有关。某些情况下和患者群体更容易发生严重的病毒性呼吸道感染(RTI)。
总结与某些人群中严重病毒性 RTI 易感性增加相关的失调免疫途径的数据。我们还描述了这些易感人群中免疫途径缺陷的共同点,这些共同点可能代表未来治疗或预防方法的潜在目标。
我们在 Medline、Scopus 和 Google Scholar 上进行了免费搜索,以寻找关注潜在免疫功能障碍机制的研究,这些机制可能与患有妊娠、肥胖、糖尿病、高血压、心血管疾病、哮喘、慢性阻塞性肺疾病(COPD)、慢性肾脏病和极端年龄等疾病的易感人群中的严重病毒性 RTI 有关。我们考虑了临床前/动物数据、原始人类研究和综述。
衰老、肥胖和糖尿病导致先天和适应性免疫反应在数量和质量上受到损害,最明显的变化影响 T 细胞。此外,所谓的炎症衰老导致这些情况下的慢性低度炎症。瘦素水平升高尤其会影响肥胖人群的免疫系统,而瘦素失调在哮喘和 COPD 发病机制中发挥作用。针对鼻病毒,I 型和 III 型干扰素(IFN)的产生不足会导致哮喘恶化。在妊娠期间也记录到针对流感和鼻病毒的 IFN 产生相似衰减。在饮食诱导的肥胖小鼠和肥胖个体中也发现了 I 型 IFN 反应减弱。
衰老和各种慢性疾病(如糖尿病、肥胖、哮喘、COPD、慢性肾脏病和高血压)伴随的免疫衰老和慢性低度炎症导致病毒呼吸道感染后观察到的不良结果。受影响的常见途径可能代表潜在的未来治疗靶点。