• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

COVID-19 的治疗策略:进展与经验教训。

Therapeutic strategies for COVID-19: progress and lessons learned.

机构信息

Xiangya School of Public Health, Central South University; Hunan Children's Hospital, Changsha, China.

Institute of Molecular Medicine & German Center for Infection Research (DZIF), University of Lübeck, Lübeck, Germany.

出版信息

Nat Rev Drug Discov. 2023 Jun;22(6):449-475. doi: 10.1038/s41573-023-00672-y. Epub 2023 Apr 19.

DOI:10.1038/s41573-023-00672-y
PMID:37076602
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10113999/
Abstract

The coronavirus disease 2019 (COVID-19) pandemic has stimulated tremendous efforts to develop therapeutic strategies that target severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and/or human proteins to control viral infection, encompassing hundreds of potential drugs and thousands of patients in clinical trials. So far, a few small-molecule antiviral drugs (nirmatrelvir-ritonavir, remdesivir and molnupiravir) and 11 monoclonal antibodies have been marketed for the treatment of COVID-19, mostly requiring administration within 10 days of symptom onset. In addition, hospitalized patients with severe or critical COVID-19 may benefit from treatment with previously approved immunomodulatory drugs, including glucocorticoids such as dexamethasone, cytokine antagonists such as tocilizumab and Janus kinase inhibitors such as baricitinib. Here, we summarize progress with COVID-19 drug discovery, based on accumulated findings since the pandemic began and a comprehensive list of clinical and preclinical inhibitors with anti-coronavirus activities. We also discuss the lessons learned from COVID-19 and other infectious diseases with regard to drug repurposing strategies, pan-coronavirus drug targets, in vitro assays and animal models, and platform trial design for the development of therapeutics to tackle COVID-19, long COVID and pathogenic coronaviruses in future outbreaks.

摘要

2019 年冠状病毒病(COVID-19)大流行激发了巨大的努力,以开发针对严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)和/或人类蛋白的治疗策略来控制病毒感染,其中包括数百种潜在药物和数千名临床试验患者。到目前为止,已有几种小分子抗病毒药物(nirmatrelvir-ritonavir、remdesivir 和 molnupiravir)和 11 种单克隆抗体被用于 COVID-19 的治疗,大多数需要在症状出现后 10 天内给药。此外,患有严重或危急 COVID-19 的住院患者可能受益于先前批准的免疫调节药物治疗,包括地塞米松等糖皮质激素、托珠单抗等细胞因子拮抗剂和巴瑞替尼等 Janus 激酶抑制剂。在这里,我们根据大流行开始以来的累积发现以及具有抗冠状病毒活性的临床和临床前抑制剂的综合清单,总结了 COVID-19 药物发现的进展。我们还讨论了从 COVID-19 和其他传染病中吸取的经验教训,涉及药物再利用策略、泛冠状病毒药物靶点、体外检测和动物模型,以及针对开发治疗 COVID-19、长期 COVID 和未来爆发的致病性冠状病毒的治疗方法的平台试验设计。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0df/10113999/f7b258f4003d/41573_2023_672_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0df/10113999/36a4039dc204/41573_2023_672_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0df/10113999/8a6b6af3a6d2/41573_2023_672_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0df/10113999/d9671e1b7f56/41573_2023_672_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0df/10113999/5ae685267d55/41573_2023_672_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0df/10113999/96073cbb82ae/41573_2023_672_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0df/10113999/a7b0676ced26/41573_2023_672_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0df/10113999/6f9d148d454a/41573_2023_672_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0df/10113999/a550d14e8baf/41573_2023_672_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0df/10113999/f7b258f4003d/41573_2023_672_Fig9_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0df/10113999/36a4039dc204/41573_2023_672_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0df/10113999/8a6b6af3a6d2/41573_2023_672_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0df/10113999/d9671e1b7f56/41573_2023_672_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0df/10113999/5ae685267d55/41573_2023_672_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0df/10113999/96073cbb82ae/41573_2023_672_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0df/10113999/a7b0676ced26/41573_2023_672_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0df/10113999/6f9d148d454a/41573_2023_672_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0df/10113999/a550d14e8baf/41573_2023_672_Fig8_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d0df/10113999/f7b258f4003d/41573_2023_672_Fig9_HTML.jpg

相似文献

1
Therapeutic strategies for COVID-19: progress and lessons learned.COVID-19 的治疗策略:进展与经验教训。
Nat Rev Drug Discov. 2023 Jun;22(6):449-475. doi: 10.1038/s41573-023-00672-y. Epub 2023 Apr 19.
2
Current status of antivirals and druggable targets of SARS CoV-2 and other human pathogenic coronaviruses.SARS-CoV-2 及其他人类致病冠状病毒的抗病毒药物和可用药靶的现状。
Drug Resist Updat. 2020 Dec;53:100721. doi: 10.1016/j.drup.2020.100721. Epub 2020 Aug 26.
3
Monoclonal Antibody Therapy For High-Risk Coronavirus (COVID 19) Patients With Mild To Moderate Disease Presentations (Archived)针对轻度至中度症状的高危冠状病毒(COVID-19)患者的单克隆抗体疗法(存档)
4
Progress, pitfalls, and path forward of drug repurposing for COVID-19 treatment.COVID-19 治疗药物再利用的进展、陷阱和前进道路。
Ther Adv Respir Dis. 2022 Jan-Dec;16:17534666221132736. doi: 10.1177/17534666221132736.
5
Contemporary narrative review of treatment options for COVID-19.当代关于 COVID-19 治疗方法的叙事性综述。
Respirology. 2021 Aug;26(8):745-767. doi: 10.1111/resp.14106. Epub 2021 Jul 8.
6
Current Strategies of Antiviral Drug Discovery for COVID-19.新型冠状病毒肺炎抗病毒药物研发的当前策略
Front Mol Biosci. 2021 May 13;8:671263. doi: 10.3389/fmolb.2021.671263. eCollection 2021.
7
Remdesivir against COVID-19 and Other Viral Diseases.瑞德西韦治疗 COVID-19 及其他病毒性疾病。
Clin Microbiol Rev. 2020 Oct 14;34(1). doi: 10.1128/CMR.00162-20. Print 2020 Dec 16.
8
Treatment Options for Patients With Mild-to-Moderate Coronavirus Disease 2019 in Korea.韩国轻度至中度 2019 冠状病毒病患者的治疗选择。
J Korean Med Sci. 2022 Dec 12;37(48):e352. doi: 10.3346/jkms.2022.37.e352.
9
Viral target and metabolism-based rationale for combined use of recently authorized small molecule COVID-19 medicines: Molnupiravir, nirmatrelvir, and remdesivir.基于病毒靶点和代谢的原理,联合使用最近获得授权的小分子 COVID-19 药物:莫努匹韦、奈玛特韦和瑞德西韦。
Fundam Clin Pharmacol. 2023 Aug;37(4):726-738. doi: 10.1111/fcp.12889. Epub 2023 Mar 25.
10
A review on the current approaches and perspectives of Covid-19 treatment.关于新冠病毒治疗的现有方法和观点的综述。
Pol Merkur Lekarski. 2024;52(3):337-346. doi: 10.36740/Merkur202403111.

引用本文的文献

1
A Bifunctional SARS-CoV-2 Entry Inhibitor Targeting the Host Protease TMPRSS2 and Viral Spike Protein HR1 Region.一种靶向宿主蛋白酶TMPRSS2和病毒刺突蛋白HR1区域的双功能SARS-CoV-2进入抑制剂。
Int J Mol Sci. 2025 Aug 26;26(17):8289. doi: 10.3390/ijms26178289.
2
Recent Advances in the Development of Metal-Glycoconjugates for Medicinal Applications.用于医学应用的金属糖缀合物开发的最新进展
Molecules. 2025 Aug 29;30(17):3537. doi: 10.3390/molecules30173537.
3
Divergent resistance pathways amongst SARS-CoV-2 PLpro inhibitors highlight the need for scaffold diversity.

本文引用的文献

1
Oral Sabizabulin for High-Risk, Hospitalized Adults with Covid-19: Interim Analysis.口服沙比沙布林治疗 COVID-19 高危住院成人:中期分析。
NEJM Evid. 2022 Sep;1(9):EVIDoa2200145. doi: 10.1056/EVIDoa2200145. Epub 2022 Jul 6.
2
Early Treatment with Pegylated Interferon Lambda for Covid-19.聚乙二醇干扰素 λ 早期治疗 COVID-19。
N Engl J Med. 2023 Feb 9;388(6):518-528. doi: 10.1056/NEJMoa2209760.
3
Meplazumab in hospitalized adults with severe COVID-19 (DEFLECT): a multicenter, seamless phase 2/3, randomized, third-party double-blind clinical trial.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)木瓜蛋白酶样蛋白酶(PLpro)抑制剂之间不同的抗性途径凸显了支架多样性的必要性。
PLoS Pathog. 2025 Sep 5;21(9):e1013468. doi: 10.1371/journal.ppat.1013468. eCollection 2025 Sep.
4
Population Pharmacokinetic Modeling Analysis of ASC10, a Novel Antiviral Agent Targeted COVID-19, in Chinese Healthy Subjects.新型抗新冠病毒药物ASC10在中国健康受试者中的群体药代动力学建模分析
Drug Des Devel Ther. 2025 Aug 26;19:7393-7404. doi: 10.2147/DDDT.S517282. eCollection 2025.
5
Impact of COVID-19 on Hematologic Cancer Patients: Insights From the Late Pandemic Phase.2019冠状病毒病对血液系统癌症患者的影响:大流行后期阶段的见解
Cancer Med. 2025 Aug;14(15):e71112. doi: 10.1002/cam4.71112.
6
SARS-CoV-2 Pneumonia: Advances in Diagnosis and Treatment.严重急性呼吸综合征冠状病毒2型肺炎:诊断与治疗进展
Microorganisms. 2025 Jul 31;13(8):1791. doi: 10.3390/microorganisms13081791.
7
Single-dose infusion of engineered viral receptor binding domain confers rapid and durable protection against viral infection.单剂量输注工程化病毒受体结合域可提供针对病毒感染的快速且持久的保护。
Commun Biol. 2025 Aug 25;8(1):1279. doi: 10.1038/s42003-025-08704-6.
8
Long-Circulating Nanobody Confers Durable Prophylaxis against Severe Acute Respiratory Syndrome Coronavirus 2 Omicron Infection.长效循环纳米抗体赋予对严重急性呼吸综合征冠状病毒2奥密克戎感染的持久预防作用。
Adv Nanobiomed Res. 2025 Aug;5(8). doi: 10.1002/anbr.202400214. Epub 2025 Jun 27.
9
SOCS Proteins: Key Players in Immune Regulation During SARS-CoV-2 Infection.SOCS蛋白:新冠病毒感染期间免疫调节的关键参与者
Eur J Immunol. 2025 Aug;55(8):e51645. doi: 10.1002/eji.202451645.
10
The C-terminal Domain of SARS-CoV-2 nsp8 is a Molten Globule in the Absence of Binding Partners.严重急性呼吸综合征冠状病毒2(SARS-CoV-2)非结构蛋白8(nsp8)的C末端结构域在没有结合伴侣的情况下是一种熔球态。
J Mol Biol. 2025 Aug 19;437(21):169400. doi: 10.1016/j.jmb.2025.169400.
美泊利单抗治疗住院的重症 COVID-19 成年患者(DEFLECT):一项多中心、无缝隙 2/3 期、随机、第三方双盲临床试验。
Signal Transduct Target Ther. 2023 Jan 30;8(1):46. doi: 10.1038/s41392-023-01323-9.
4
Innate immune evasion strategies of SARS-CoV-2.SARS-CoV-2 的先天免疫逃避策略。
Nat Rev Microbiol. 2023 Mar;21(3):178-194. doi: 10.1038/s41579-022-00839-1. Epub 2023 Jan 11.
5
VV116 versus Nirmatrelvir-Ritonavir for Oral Treatment of Covid-19.VV116 对比奈玛特韦片/利托那韦片组合药物用于 COVID-19 口服治疗。
N Engl J Med. 2023 Feb 2;388(5):406-417. doi: 10.1056/NEJMoa2208822. Epub 2022 Dec 28.
6
Molnupiravir plus usual care versus usual care alone as early treatment for adults with COVID-19 at increased risk of adverse outcomes (PANORAMIC): an open-label, platform-adaptive randomised controlled trial.莫努匹韦联合常规治疗与单纯常规治疗用于 COVID-19 高风险不良结局成人患者早期治疗的比较(PANORAMIC):一项开放标签、平台适应性随机对照试验。
Lancet. 2023 Jan 28;401(10373):281-293. doi: 10.1016/S0140-6736(22)02597-1. Epub 2022 Dec 22.
7
Interfering with nucleotide excision by the coronavirus 3'-to-5' exoribonuclease.干扰冠状病毒 3'-5'外切核糖核酸酶的核苷酸切除。
Nucleic Acids Res. 2023 Jan 11;51(1):315-336. doi: 10.1093/nar/gkac1177.
8
Long-term (180-Day) Outcomes in Critically Ill Patients With COVID-19 in the REMAP-CAP Randomized Clinical Trial.REMAP-CAP 随机临床试验中 COVID-19 危重症患者的长期(180 天)结局。
JAMA. 2023 Jan 3;329(1):39-51. doi: 10.1001/jama.2022.23257.
9
Efficacy and Safety of Ensitrelvir in Patients With Mild-to-Moderate Coronavirus Disease 2019: The Phase 2b Part of a Randomized, Placebo-Controlled, Phase 2/3 Study.恩赛特韦在轻至中度 2019 冠状病毒病患者中的疗效和安全性:一项随机、安慰剂对照、2/3 期研究的 2b 期部分。
Clin Infect Dis. 2023 Apr 17;76(8):1403-1411. doi: 10.1093/cid/ciac933.
10
FXR inhibition may protect from SARS-CoV-2 infection by reducing ACE2.法尼醇 X 受体(FXR)抑制可能通过降低 ACE2 来预防严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)感染。
Nature. 2023 Mar;615(7950):134-142. doi: 10.1038/s41586-022-05594-0. Epub 2022 Dec 5.