Evidence map›Paper›PMID 35962188›Full record

ArticleCommunications biology2022

PIKfyve-specific inhibitors restrict replication of multiple coronaviruses in vitro but not in a murine model of COVID-19.

James Logue, Arup R Chakraborty, Robert Johnson, Girija Goyal, Melissa Rodas, Louis J Taylor, Lauren Baracco, Marisa E McGrath, Robert Haupt, Brooke A Furlong and 8 more

Open access · goldAbstract read
In one paragraph

Article in Communications biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.6field-weighted citation impact, top 15% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Development of a Second-Generation,Journal of medicinal chemistry · 2025
    Article
  7. Review
  8. Review
  9. Article
  10. 1-L Transcription of SARS-CoV-2 Spike Protein S1 Subunit.International journal of molecular sciences · 2024
    Article
  11. Article
  12. Preparing for the next viral threat with broad-spectrum antivirals.The Journal of clinical investigation · 2023
    Review
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

18 authors at 4 institutions in 1 country.

James LogueDepartment of Microbiology and Immunology, University of Maryland, School of Medicine, 685 West Baltimore St, Baltimore, MD, 21201, USA.ORCID 0000-0002-7410-9741
Arup R ChakrabortyDivision of Developmental Biology, National Institute of Child Health & Human Development, National Institutes of Health, Bethesda, MD, 20892-2790, USA.
Robert JohnsonDepartment of Microbiology and Immunology, University of Maryland, School of Medicine, 685 West Baltimore St, Baltimore, MD, 21201, USA.ORCID 0000-0002-1976-7688
Girija GoyalWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, 02115, USA.
Melissa RodasWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, 02115, USA.
Louis J TaylorDepartment of Microbiology and Immunology, University of Maryland, School of Medicine, 685 West Baltimore St, Baltimore, MD, 21201, USA.ORCID 0000-0002-6993-5838
Lauren BaraccoDepartment of Microbiology and Immunology, University of Maryland, School of Medicine, 685 West Baltimore St, Baltimore, MD, 21201, USA.
Marisa E McGrathDepartment of Microbiology and Immunology, University of Maryland, School of Medicine, 685 West Baltimore St, Baltimore, MD, 21201, USA.ORCID 0000-0002-7451-4958
Robert HauptDepartment of Microbiology and Immunology, University of Maryland, School of Medicine, 685 West Baltimore St, Baltimore, MD, 21201, USA.
Brooke A FurlongWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, 02115, USA.ORCID 0000-0001-7584-0707
Mercy SoongWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, 02115, USA.
Pranav PrabhalaWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, 02115, USA.
Viktor HorvathWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, 02115, USA.ORCID 0000-0001-9957-1521
Kenneth E CarlsonWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, 02115, USA.
Stuart WestonDepartment of Microbiology and Immunology, University of Maryland, School of Medicine, 685 West Baltimore St, Baltimore, MD, 21201, USA.ORCID 0000-0001-9840-2953
Donald E IngberWyss Institute for Biologically Inspired Engineering, Harvard University, Boston, MA, 02115, USA.ORCID 0000-0002-4319-6520
Melvin L DePamphilisDivision of Developmental Biology, National Institute of Child Health & Human Development, National Institutes of Health, Bethesda, MD, 20892-2790, USA.
Matthew B FriemanDepartment of Microbiology and Immunology, University of Maryland, School of Medicine, 685 West Baltimore St, Baltimore, MD, 21201, USA. mfrieman@som.umaryland.edu.ORCID 0000-0003-0107-0775
University of Maryland, Baltimore · USHarvard University · USNational Institutes of Health · USBoston Children's Hospital · US

Funding

FELLOWSHIP TRAINING PROGRAM IN VACCINOLOGYT32AI007524 · NIAID · UNIVERSITY OF MARYLAND BALTIMORE · PI Marcelo B. Sztein · 1997 to 2026
$6.4M
INITIATION OF DNA REPLICATION IN MAMMILIAN CHROMOSOMESZ01HD000506 · NICHD · EUNICE KENNEDY SHRIVER NATIONAL INSTITUTE OF CHILD HEALTH & HUMAN DEVELOPMENT · PI DEPAMPHILIS, MELVIN · 1996 to 2008
$1.7M
Intramural NIH HHS Z01 HD000506NIAID NIH HHS T32 AI007524
6 · The paper itself

Abstract

The ongoing COVID-19 pandemic has claimed more than 6 million lives and continues to test the world economy and healthcare systems. To combat this pandemic, the biological research community has shifted efforts to the development of medical countermeasures, including vaccines and therapeutics. However, to date, the only small molecules approved for the treatment of COVID-19 in the United States are the nucleoside analogue Remdesivir and the protease inhibitor Paxlovid, though multiple compounds have received Emergency Use Authorization and many more are currently being tested in human efficacy trials. One such compound, Apilimod, is being considered as a COVID-19 therapeutic in a Phase II efficacy trial. However, at the time of writing, there are no published efficacy data in human trials or animal COVID-19 models. Here we show that, while Apilimod and other PIKfyve inhibitors have potent antiviral activity in various cell lines against multiple human coronaviruses, these compounds worsen disease in a COVID-19 murine model when given prophylactically or therapeutically.

Indexed as

COVID-19 Drug TreatmentAnimalsAntiviral AgentsDisease Models, AnimalHumansMicePandemicsPhosphatidylinositol 3-KinasesProtease InhibitorsAntiviral AgentsPhosphatidylinositol 3-KinasesPIKFYVE protein, humanPikfyve protein, mouseProtease Inhibitors

Identifiers

PMID35962188
PMCPMC9372968
OpenAlexW4291145320

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.