Drugs against SARS‐CoV‐2: What do we know about their mode of action?

临床试验 2019年冠状病毒病(COVID-19) 严重急性呼吸综合征冠状病毒2型(SARS-CoV-2) 医学 疾病 大流行 重症监护医学 药理学 传染病(医学专业) 内科学
作者
Coralie Valle,Baptiste Martin,Franck Touret,Ashleigh Shannon,Bruno Canard,Jean‐Claude Guillemot,Bruno Coutard,Étienne Decroly
出处
期刊:Reviews in Medical Virology [Wiley]
卷期号:30 (6): 1-10 被引量:29
标识
DOI:10.1002/rmv.2143
摘要

The health emergency caused by the recent Covid-19 pandemic highlights the need to identify effective treatments against the virus causing this disease (SARS-CoV-2). The first clinical trials have been testing repurposed drugs that show promising anti-SARS-CoV-2 effects in cultured cells. Although more than 2400 clinical trials are already under way, the actual number of tested compounds is still limited to approximately 20, alone or in combination. In addition, knowledge on their mode of action (MoA) is currently insufficient. Their first results reveal some inconsistencies and contradictory results and suggest that cohort size and quality of the control arm are two key issues for obtaining rigorous and conclusive results. Moreover, the observed discrepancies might also result from differences in the clinical inclusion criteria, including the possibility of early treatment that may be essential for therapy efficacy in patients with Covid-19. Importantly, efforts should also be made to test new compounds with a documented MoA against SARS-CoV-2 in clinical trials. Successful treatment will probably be based on multitherapies with antiviral compounds that target different steps of the virus life cycle. Moreover, a multidisciplinary approach that combines artificial intelligence, compound docking, and robust in vitro and in vivo assays will accelerate the development of new antiviral molecules. Finally, large retrospective studies on hospitalized patients are needed to evaluate the different treatments with robust statistical tools and to identify the best treatment for each Covid-19 stage. This review describes different candidate antiviral strategies for Covid-19, by focusing on their mechanism of action.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
大幅提高文件上传限制,最高150M (2024-4-1)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
keke发布了新的文献求助10
1秒前
2秒前
深情丸子发布了新的文献求助30
2秒前
Janvenns发布了新的文献求助10
2秒前
3秒前
3秒前
3秒前
大列巴完成签到,获得积分10
4秒前
CodeCraft应助行川采纳,获得10
4秒前
4秒前
英俊的铭应助酷炫的友易采纳,获得10
5秒前
初期发布了新的文献求助10
5秒前
quhayley应助Billy采纳,获得10
8秒前
Jiang湫完成签到 ,获得积分10
8秒前
隐形曼青应助Delia采纳,获得10
9秒前
zhaoman完成签到,获得积分10
9秒前
9秒前
9秒前
星河发布了新的文献求助10
9秒前
Hcir完成签到 ,获得积分10
10秒前
10秒前
嘻嘻发布了新的文献求助10
11秒前
静不净发布了新的文献求助10
12秒前
Lilili发布了新的文献求助10
12秒前
池寒1发布了新的文献求助10
12秒前
彭于晏应助小小采纳,获得10
13秒前
13秒前
胡恒源发布了新的文献求助10
13秒前
13秒前
狂野元枫完成签到,获得积分10
14秒前
科研通AI2S应助xzh采纳,获得10
15秒前
hh发布了新的文献求助10
16秒前
纳米粒子完成签到,获得积分10
16秒前
直率的宛海完成签到,获得积分10
16秒前
93完成签到 ,获得积分10
17秒前
17秒前
通宵完成签到 ,获得积分10
17秒前
17秒前
18秒前
MiManchi完成签到,获得积分10
18秒前
高分求助中
Evolution 10000
Sustainability in Tides Chemistry 2800
The Young builders of New china : the visit of the delegation of the WFDY to the Chinese People's Republic 1000
юрские динозавры восточного забайкалья 800
A new approach of magnetic circular dichroism to the electronic state analysis of intact photosynthetic pigments 500
Diagnostic immunohistochemistry : theranostic and genomic applications 6th Edition 500
Chen Hansheng: China’s Last Romantic Revolutionary 500
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 催化作用 物理化学 免疫学 量子力学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 3148856
求助须知:如何正确求助?哪些是违规求助? 2799869
关于积分的说明 7837518
捐赠科研通 2457441
什么是DOI,文献DOI怎么找? 1307837
科研通“疑难数据库(出版商)”最低求助积分说明 628280
版权声明 601685