Emerging pharmacotherapy for COVID-19.
Adenosine Monophosphate
/ analogs & derivatives
Alanine
/ analogs & derivatives
Anti-Inflammatory Agents
/ therapeutic use
Antiviral Agents
/ therapeutic use
Betacoronavirus
COVID-19
Coronavirus Infections
/ complications
Cytokines
/ physiology
Enzyme Inhibitors
/ therapeutic use
Humans
Hydroxychloroquine
/ therapeutic use
Pandemics
Pneumonia, Viral
/ complications
SARS-CoV-2
ACE2
ARDS
COVID-19
SARS-CoV-2
TMPRSS2
antivirals
comorbidity
corticosteroid
cytokine
hyperinflammation
pneumonia
Journal
The journal of the Royal College of Physicians of Edinburgh
ISSN: 2042-8189
Titre abrégé: J R Coll Physicians Edinb
Pays: England
ID NLM: 101144324
Informations de publication
Date de publication:
06 2020
06 2020
Historique:
entrez:
23
6
2020
pubmed:
23
6
2020
medline:
3
7
2020
Statut:
ppublish
Résumé
Broadly speaking, pharmacological treatments for COVID-19 can be divided into those acting on upstream pathways early on in the disease process via suppression of viral replication or by inhibiting cell entry, and those acting on downstream pathways later on via selective attenuation of the adaptive immune cytokine-mediated inflammatory response. The antiviral drug remdesivir has been shown to shorten duration of disease while interferon beta-1b may speed up viral clearance. The results with hydroxychloroquine have thus far been rather disappointing. Trials with selective cytokine blockers including anti-interleukin-1 (anti-IL-1) and anti-interleukin-6 (anti-IL-6), have shown some promise in more severe cases, with further confirmation being required from large-scale phase-3 randomised controlled trials. The likelihood is that combination therapy addressing both upstream and downstream pathways may be required to prevent progression of severe COVID-19 infection in susceptible older patients with comorbidities and we believe further studies are now warranted to specifically target such at-risk groups who are more prone to worse outcomes.
Identifiants
pubmed: 32568282
doi: 10.4997/JRCPE.2020.210
doi:
Substances chimiques
Anti-Inflammatory Agents
0
Antiviral Agents
0
Cytokines
0
Enzyme Inhibitors
0
remdesivir
3QKI37EEHE
Adenosine Monophosphate
415SHH325A
Hydroxychloroquine
4QWG6N8QKH
Alanine
OF5P57N2ZX
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
133-137Déclaration de conflit d'intérêts
Dr Kuo reports personal fees from AstraZeneca, personal fees from Chiesi, personal fees from Circassia, outside the submitted work. Dr Lipworth reports no competing interests with respect to the submitted work, and reports personal fees and non-financial support from AstraZeneca, grants, personal fees and non-financial support from Chiesi and Sanofi, personal fees from Cipla, Novartis, Lupin and Dr Reddys, from Glenmark, grants and personal fees from Teva and Mylan, personal fees from Vectura, outside the submitted work; Dr Lipworth’s son is an employee of AstraZeneca.