Evaluation of Artemisia as an Effective Combination Therapy Against SARS-CoV-2 Infection

青蒿作为对抗 SARS-CoV-2 感染的有效联合疗法的评估

• 批准号: 10625445
• 负责人: Joshua Kellogg
• 金额: $ 25万
• 依托单位: PENNSYLVANIA STATE UNIVERSITY, THE
• 依托单位国家: 美国
• 财政年份: 2022
• 资助国家: 美国
• 起止时间: 2022-05-20 至 2025-04-30
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10625445
• 关键词: 2019-nCoV; ACE2; Address; Anti-Inflammatory Agents; Antimalarials; Antiviral Agents; Artemisia; Artemisia annua; Artemisinins; Asteraceae; Bioinformatics; Biology; Body Weight decreased; Botanicals; COVID-19; COVID-19 pandemic; Cells; Cessation of life; Chemicals; Clinical Research; Combined Modality Therapy; Coronavirus; Country; Dangerousness; Data; Dexamethasone; Disease; Disease Marker; Disease Outbreaks; Dose; Drug Combinations; Educational process of instructing; Ethnopharmacology; Evaluation; Fever; Goals; Healthcare Systems; Hour; Human; Humanities; In Vitro; Infection; Inflammation; Inflammatory; Life Cycle Stages; Measures; Medicinal Plants; Medicine; Meta-Analysis; Modality; Modeling; Mus; Mutate; Natural Products; Natural Products Chemistry; Oral; Outcome; Paxlovid; Persons; Pharmaceutical Preparations; Pharmacology; Phase; Plant Extracts; Plant Leaves; Plants; Population; Preparation; Primary Health Care; Publishing; Readiness; Recording of previous events; Resources; Rest; SARS-CoV-2 infection; SARS-CoV-2 inhibitor; SARS-CoV-2 variant; Testing; Therapeutic; Therapeutic Studies; Transgenic Mice; Uncertainty; Vaccines; Variant; Viral; Viral Load result; Viral Physiology; Virus; Water; coronavirus pandemic; cytotoxic; disorder prevention; efficacy testing; experience; fighting; human disease; in vivo; indexing; inflammatory marker; innovation; molnupiravir; mouse model; novel; pandemic disease; pathogenic virus; prophylactic; remdesivir; stem; success; synergism; tool; vaccine access; vaccine hesitancy; variants of concern; viral outbreak; virology

ABSTRACT Viruses are cleverly dangerous; they jump from species to species, mutate to evade vaccines and single antiviral drugs, and cause many human diseases and deaths. A notorious current example is Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2). As we witness daily, the coronavirus pandemic reveals gaping holes in the US healthcare system and how woefully unprepared we are for wide-spread viral outbreaks. Two years into the pandemic we have three antiviral drugs (remdesivir, molnupiravir, and paxlovid and a single anti-inflammatory (dexamethasone). Thus, there remains an unmet need for drugs to fight the virus and the inflammatory sequelae of infection. Recently available vaccines comprise a boon to stopping this pandemic, but rollout, distribution, vaccine hesitancy, and the continuing emergence of variants of concern (VOC) hinder progress towards this goal. Because of these uncertainties, many people have turned to natural products with the hope that these untested supplements will keep them safe and healthy. In fact, nearly 20% of the US population uses natural products (including plant-based or botanical preparations) for treatment or prevention of disease. The use of plant-based medicines is even more prevalent in resource-limited countries, where for many people they constitute a primary health care modality. This R21 proposal stems from the recent finding by our team that extracts from the plant Artemisia annua L. (Asteraceae) (aka A. annua, qinghao, sweet wormwood, annual wormwood, sweet annie), potently inhibits wild type SARS-CoV-2 and VOC infection in vitro. Based on our recently published and preliminary data, we hypothesize that A. annua contains mixtures of compounds that synergistically inhibit SARS-CoV-2 and virus-induced inflammation in vivo. To address the hypothesis, the Weathers, Polyak, Fuller, and Kellogg labs will merge their complementary expertise in plant ethnopharmacology the pharmacology of historically used medicinal plants), in vitro and in vivo virology, and natural product chemistry, and to conduct two Specific Aims that will demonstrate the in vivo antiviral activity of A. annua extracts in the human ACE-2 transgenic mouse model of SARS-CoV-2 infection and disease (AIM 1). We will also a) define the natural product(s) that confer antiviral activity, b) whether virus suppression arises through synergistic combinations of compounds in A. annua, and c) begin to decipher mechanisms of antiviral action (AIM 2). As such, this project is expected to provide new tools for the battle against COVID-19 and potentially enhance global preparedness for the next virus outbreak, which history has taught us will most certainly occur.

摘要 病毒是聪明的危险;它们从一个物种跳到另一个物种，变异以逃避疫苗和单一的抗病毒药物 药物，并导致许多人类疾病和死亡。当前一个臭名昭著的例子是严重急性呼吸道感染 冠状病毒2型综合征（SARS-CoV-2）。正如我们每天所看到的，冠状病毒大流行揭示了巨大的漏洞 美国医疗体系的危机，以及我们对大范围病毒爆发的准备不足。两年 我们有三种抗病毒药物（瑞德西韦、莫努匹拉韦和帕昔洛韦）和一种抗炎药（地塞米松）。因此，对于对抗病毒和感染的炎性后遗症的药物仍然存在未满足的需求。最近可用的疫苗包括阻止这种流行病的布恩，但推出，分配，疫苗犹豫，并不断出现的变异的关注（VOC）阻碍了这一目标的进展。由于这些不确定性，许多人转向天然产品， 希望这些未经测试的补充剂能让他们安全健康。事实上，近20%的美国人口使用天然产品（包括植物或植物制剂）来治疗或预防疾病。在资源有限的国家，植物药物的使用更为普遍，对许多人来说，植物药物是一种初级保健方式。这个R21的建议源于我们的团队最近的发现，从植物青蒿提取物。（Asteraceae）（aka A.青蒿青蒿青蒿 annual wormwood，sweet annie），在体外有效抑制野生型SARS-CoV-2和VOC感染。根据我们最近发表的初步数据，我们假设A。annua含有在体内协同抑制SARS-CoV-2和病毒诱导的炎症的化合物的混合物。为了解决这一假设，Weathers、Polyak、Fuller和凯洛格实验室将把他们在植物民族药理学（历史上使用的药用植物的药理学）、体外和体内病毒学以及天然产物方面的互补专业知识结合起来。 化学，并进行两个特定的目的，将证明在体内抗病毒活性的A。annua提取物在SARS-CoV-2感染和疾病的人ACE-2转基因小鼠模型（AIM 1）中的作用。我们还将a）定义赋予抗病毒活性的天然产物，B）是否通过A中化合物的协同组合产生病毒抑制。annua，和c）开始破译抗病毒作用的机制（AIM 2）。因此，该项目有望为抗击COVID-19提供新的工具，并有可能加强全球对下一次病毒爆发的准备，历史告诉我们，下一次病毒爆发肯定会发生。