Evidence map›Paper›PMID 34319150›Full record

ReviewClinical microbiology reviews2021

SARS-CoV-2 Antiviral Therapy.

Kaiming Tao, Philip L Tzou, Janin Nouhin, Hector Bonilla, Prasanna Jagannathan, Robert W Shafer

Open access · greenAbstract readReview
In one paragraph

Review in Clinical microbiology reviews, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

61 citing papers in PubMed, 99 citations in OpenAlex.

  1. Article
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  15. Article
  16. Intranasal neomycin evokes broad-spectrum antiviral immunity in the upper respiratory tract.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  17. The SARS-CoV-2 MACS synthetic biology · 2024
    Article
  18. Article
  19. Article
  20. Structure-based design of SARS-CoV-2 papain-like protease inhibitors.European journal of medicinal chemistry · 2024
    Article

1 more citing papers are in PubMed but not listed here.

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

6 authors at 1 institution in 1 country.

Kaiming TaoDivision of Infectious Diseases, Department of Medicine, Stanford University, Stanford, California, USA.ORCID 0000-0001-8731-1271
Philip L TzouDivision of Infectious Diseases, Department of Medicine, Stanford University, Stanford, California, USA.ORCID 0000-0002-2876-1552
Janin NouhinDivision of Infectious Diseases, Department of Medicine, Stanford University, Stanford, California, USA.
Hector BonillaDivision of Infectious Diseases, Department of Medicine, Stanford University, Stanford, California, USA.
Prasanna JagannathanDivision of Infectious Diseases, Department of Medicine, Stanford University, Stanford, California, USA.ORCID 0000-0001-6305-758X
Robert W ShaferDivision of Infectious Diseases, Department of Medicine, Stanford University, Stanford, California, USA.
Stanford University · US

Funding

Computational models of naturally acquired immunity to falciparum malariaU01AI150741 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BUTTE, ATUL J, GREENHOUSE, BRYAN R · 2020 to 2024
$7.4M
HIV Drug Resistance DatabaseR24AI136618 · NIAID · STANFORD UNIVERSITY · PI ROBERT William SHAFER · 2018 to 2026
$7.3M
Stanford TRANSFORM I2T ProgramR25AI147369 · NIAID · STANFORD UNIVERSITY · PI CHERTOW, GLENN MATTHEW, SINGH, UPINDER · 2019 to 2023
$1.8M
NIAID NIH HHS R24 AI136618NIAID NIH HHS R25 AI147369NIAID NIH HHS U01 AI150741
6 · The paper itself

Abstract

The development of effective antiviral therapy for COVID-19 is critical for those awaiting vaccination, as well as for those who do not respond robustly to vaccination. This review summarizes 1 year of progress in the race to develop antiviral therapies for COVID-19, including research spanning preclinical and clinical drug development efforts, with an emphasis on antiviral compounds that are in clinical development or that are high priorities for clinical development. The review is divided into sections on compounds that inhibit SARS-CoV-2 enzymes, including its polymerase and proteases; compounds that inhibit virus entry, including monoclonal antibodies; interferons; and repurposed drugs that inhibit host processes required for SARS-CoV-2 replication. The review concludes with a summary of the lessons to be learned from SARS-CoV-2 drug development efforts and the challenges to continued progress.

Indexed as

COVID-19SARS-CoV-2Antiviral AgentsDrug DevelopmentEndopeptidasesHumansAntiviral AgentsEndopeptidasesantiviral therapydrug repurposingmonoclonal antibodynucleoside analogsSARS-CoV-2

Identifiers

PMID34319150
PMCPMC8404831
OpenAlexW3184095558

What OpenQuestion holds

Textmetadata
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.