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减少嗜老年菌和嗜老年病毒感染中的合并症、感染率、严重程度及致死率的老年保护和衰老修复策略。

Geroprotective and senoremediative strategies to reduce the comorbidity, infection rates, severity, and lethality in gerophilic and gerolavic infections.

作者信息

Zhavoronkov Alex

机构信息

Insilico Medicine, Hong Kong Science and Technology Park (HKSTP), Tai Po, Hong Kong.

The Biogerontology Research Foundation, London, UK.

出版信息

Aging (Albany NY). 2020 Mar 31;12(8):6492-6510. doi: 10.18632/aging.102988.

Abstract

The recently identified SARS-CoV-2 betacoronavirus responsible for the COVID-19 pandemic has uncovered the age-associated vulnerability in the burden of disease and put aging research in the spotlight. The limited data available indicates that COVID-19 should be referred to as a gerolavic (from Greek, géros "old man" and epilavís, "harmful") infection because the infection rates, severity, and lethality are substantially higher in the population aged 60 and older. This is primarily due to comorbidity but may be partially due to immunosenescence, decreased immune function in the elderly, and general loss of function, fitness, and increased frailty associated with aging. Immunosenescence is a major factor affecting vaccination response, as well as the severity and lethality of infectious diseases. While vaccination reduces infection rates, and therapeutic interventions reduce the severity and lethality of infections, these interventions have limitations. Previous studies showed that postulated geroprotectors, such as sirolimus (rapamycin) and its close derivative rapalog everolimus (RAD001), decreased infection rates in a small sample of elderly patients. This article presents a review of the limited literature available on geroprotective and senoremediative interventions that may be investigated to decrease the disease burden of gerolavic infections. This article also highlights a need for rigorous clinical validation of deep aging clocks as surrogate markers of biological age. These could be used to assess the need for, and efficacy of, geroprotective and senoremediative interventions and provide better protection for elderly populations from gerolavic infections. This article does not represent medical advice and the medications described are not yet licensed or recommended as immune system boosters, as they have not undergone clinical evaluation for this purpose.

摘要

最近发现的导致COVID-19大流行的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)β冠状病毒揭示了疾病负担中与年龄相关的脆弱性,并使衰老研究成为焦点。现有有限的数据表明,COVID-19应被称为老年致病性(源自希腊语,géros意为“老人”,epilavís意为“有害的”)感染,因为60岁及以上人群的感染率、严重程度和致死率要高得多。这主要是由于合并症,但也可能部分归因于免疫衰老、老年人免疫功能下降以及与衰老相关的功能、健康普遍丧失和身体虚弱增加。免疫衰老是影响疫苗接种反应以及传染病严重程度和致死率的主要因素。虽然疫苗接种可降低感染率,治疗性干预可降低感染的严重程度和致死率,但这些干预措施都有局限性。先前的研究表明,假定的老年保护剂,如西罗莫司(雷帕霉素)及其密切衍生物雷帕霉素类似物依维莫司(RAD001),在一小部分老年患者样本中降低了感染率。本文对可用于研究以减轻老年致病性感染疾病负担的老年保护和衰老修复干预措施的有限文献进行了综述。本文还强调了对深度衰老时钟作为生物学年龄替代标志物进行严格临床验证的必要性。这些时钟可用于评估老年保护和衰老修复干预措施的必要性和疗效,并为老年人群提供更好的保护,使其免受老年致病性感染。本文不代表医学建议,所述药物尚未被许可或推荐作为免疫系统增强剂,因为它们尚未为此目的进行临床评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1731/7202545/00e48e6e4a83/aging-12-102988-g001.jpg

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