Evidence map›Paper›PMID 33572117›Full record

ArticleMicroorganisms2021

Fluoxetine Can Inhibit SARS-CoV-2 In Vitro.

Arthur Dechaumes, Magloire Pandoua Nekoua, Sandrine Belouzard, Famara Sane, Ilka Engelmann, Jean Dubuisson, Enagnon Kazali Alidjinou, Didier Hober

Open access · goldAbstract read
In one paragraph

Article in Microorganisms, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
2.5field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

28 citing papers in PubMed, 41 citations in OpenAlex.

  1. Molecular mechanisms of SARS-CoV-2 entry: implications for biomedical strategies.Microbiology and molecular biology reviews : MMBR · 2025
    Review
  2. Article
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  5. Can pharmaceutical pollution alter the spread of infectious disease? A case study using fluoxetine.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2023
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 2 institutions in 1 country.

Arthur DechaumesLaboratoire de Virologie ULR3610, Univ Lille, CHU Lille, 59000 Lille, France.
Magloire Pandoua NekouaLaboratoire de Virologie ULR3610, Univ Lille, CHU Lille, 59000 Lille, France.
Sandrine BelouzardVirologie Moléculaire et Cellulaire des Coronavirus, Centre D'infection et D'immunité de Lille, Institut Pasteur de Lille, Université de Lille, CNRS, Inserm, CHRU, 59000 Lille, France.
Famara SaneLaboratoire de Virologie ULR3610, Univ Lille, CHU Lille, 59000 Lille, France.
Ilka EngelmannLaboratoire de Virologie ULR3610, Univ Lille, CHU Lille, 59000 Lille, France.
Jean DubuissonVirologie Moléculaire et Cellulaire des Coronavirus, Centre D'infection et D'immunité de Lille, Institut Pasteur de Lille, Université de Lille, CNRS, Inserm, CHRU, 59000 Lille, France.ORCID 0000-0003-1626-7693
Enagnon Kazali AlidjinouLaboratoire de Virologie ULR3610, Univ Lille, CHU Lille, 59000 Lille, France.
Didier HoberLaboratoire de Virologie ULR3610, Univ Lille, CHU Lille, 59000 Lille, France.
Université de Lille · FRCentre National de la Recherche Scientifique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

An outbreak of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) resulted in the coronavirus disease pandemic, drastically affecting global health and economy. Though the understanding of the disease has improved, fighting the virus remains challenging. One of the strategies is repurposing existing drugs as inhibitors of SARS-CoV-2. Fluoxetine (FLX), a selective serotonin reuptake inhibitor, reportedly inhibits the replication of RNA viruses, especially Coxsackieviruses B (CVB), such as CV-B4 in vitro and in vivo. Therefore, in this study, we investigated the in vitro antiviral activity of FLX against SARS-CoV-2 in a model of acute infection. When 10 μM of FLX was added to SARS-CoV-2-infected Vero E6 cells, the virus-induced cytopathic effect was not observed. In this model, the level of infectious particles in the supernatant was lower than that in controls. The level was below the limit of detection of the assay up to day 3 post-infection when FLX was administered before viral inoculation or simultaneously followed by daily inoculation. In conclusion, FLX can inhibit SARS-CoV-2 in vitro. Further studies are needed to investigate the potential value of FLX to combat SARS-CoV-2 infections, treat SARS-CoV-2-induced diseases, and explain the antiviral mechanism of this molecule to pave way for novel treatment strategies.

Indexed as

coronavirusfluoxetinein vitroSARS-CoV-2

Identifiers

PMID33572117
PMCPMC7914627
OpenAlexW3128117861

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.