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用非瑟酮治疗熟练护理设施中的 COVID-19:COVID 时代的衰老细胞试验。

Fisetin for COVID-19 in skilled nursing facilities: Senolytic trials in the COVID era.

机构信息

Robert and Arlene Kogod Center on Aging, Mayo Clinic, Rochester, Minnesota, USA.

Division of Geriatrics and Gerontology, Mayo Clinic, Rochester, Minnesota, USA.

出版信息

J Am Geriatr Soc. 2021 Nov;69(11):3023-3033. doi: 10.1111/jgs.17416. Epub 2021 Aug 20.

Abstract

The burden of senescent cells (SnCs), which do not divide but are metabolically active and resistant to death by apoptosis, is increased in older adults and those with chronic diseases. These individuals are also at the greatest risk for morbidity and mortality from SARS-CoV-2 infection. SARS-CoV-2 complications include cytokine storm and multiorgan failure mediated by the same factors as often produced by SnCs through their senescence-associated secretory phenotype (SASP). The SASP can be amplified by infection-related pathogen-associated molecular profile factors. Senolytic agents, such as Fisetin, selectively eliminate SnCs and delay, prevent, or alleviate multiple disorders in aged experimental animals and animal models of human chronic diseases, including obesity, diabetes, and respiratory diseases. Senolytics are now in clinical trials for multiple conditions linked to SnCs, including frailty; obesity/diabetes; osteoporosis; and cardiovascular, kidney, and lung diseases, which are also risk factors for SARS-CoV-2 morbidity and mortality. A clinical trial is underway to test if senolytics decrease SARS-CoV-2 progression and morbidity in hospitalized older adults. We describe here a National Institutes of Health-funded, multicenter, placebo-controlled clinical trial of Fisetin for older adult skilled nursing facility (SNF) residents who have been, or become, SARS-CoV-2 rtPCR-positive, including the rationale for targeting fundamental aging mechanisms in such patients. We consider logistic challenges of conducting trials in long-term care settings in the SARS-CoV-2 era, including restricted access, consent procedures, methods for obtaining biospecimens and clinical data, staffing, investigational product administration issues, and potential solutions for these challenges. We propose developing a national network of SNFs engaged in interventional clinical trials.

摘要

衰老细胞(SnC)的负担在老年人和患有慢性疾病的人群中增加,这些细胞不再分裂,但代谢活跃,对凋亡有抗性。这些人也面临着最大的发病和死于 SARS-CoV-2 感染的风险。SARS-CoV-2 的并发症包括细胞因子风暴和多器官衰竭,这些都是由 SnC 通过其衰老相关分泌表型(SASP)产生的相同因素介导的。SASP 可以通过感染相关的病原体相关分子模式因素放大。Senolytic 剂,如 Fisetin,选择性地消除 SnC,并延缓、预防或缓解老年实验动物和人类慢性疾病动物模型中的多种疾病,包括肥胖、糖尿病和呼吸系统疾病。Senolytic 剂目前正在进行与 SnC 相关的多种疾病的临床试验,包括虚弱、肥胖/糖尿病、骨质疏松症以及心血管、肾脏和肺部疾病,这些也是 SARS-CoV-2 发病和死亡率的风险因素。目前正在进行一项临床试验,以测试 Senolytic 剂是否可以降低住院老年人中 SARS-CoV-2 的进展和发病率。我们在这里描述了一项由美国国立卫生研究院资助的、多中心、安慰剂对照的 Fisetin 临床试验,该试验针对的是已经或成为 SARS-CoV-2 rtPCR 阳性的老年熟练护理设施(SNF)居民,包括针对此类患者的基本衰老机制的基本原理。我们考虑了在 SARS-CoV-2 时代在长期护理环境中进行试验的逻辑挑战,包括受限的访问、同意程序、获得生物样本和临床数据的方法、人员配备、研究产品管理问题以及这些挑战的潜在解决方案。我们建议建立一个参与干预性临床试验的 SNF 国家网络。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc2c/8447437/e928dd9f22d4/JGS-69-3023-g001.jpg

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