Evidence map›Paper›PMID 34511591›Full record

ReviewDermatology (Basel, Switzerland)2021

Interferon and Toll-Like Receptor 7 Response in COVID-19: Implications of Topical Imiquimod for Prophylaxis and Treatment.

Mindy D Szeto, Jalal Maghfour, Torunn E Sivesind, Jarett Anderson, Jadesola T Olayinka, Andrina Mamo, Taylor M Runion, Robert P Dellavalle

Open access · hybridAbstract readReview
In one paragraph

Review in Dermatology (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Human genetic basis of severe or critical illness in COVID-19.Frontiers in cellular and infection microbiology · 2022
    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

8 authors at 5 institutions in 1 country.

Mindy D SzetoDepartment of Dermatology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Jalal MaghfourDepartment of Medicine, Tulane University School of Medicine, New Orleans, Louisiana, USA, jmaghfou@tulane.edu.
Torunn E SivesindDepartment of Dermatology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Jarett AndersonArizona College of Osteopathic Medicine, Midwestern University, Glendale, Arizona, USA.
Jadesola T OlayinkaCollege of Medicine, SUNY Downstate Health Sciences Center, New York, New York, USA.
Andrina MamoSchool of Medicine, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
Taylor M RunionCollege of Osteopathic Medicine, Rocky Vista University, Parker, Colorado, USA.
Robert P DellavalleDepartment of Dermatology, University of Colorado Anschutz Medical Campus, Aurora, Colorado, USA.
University of Colorado Anschutz Medical Campus · USMidwestern University · USRocky Vista University · USSUNY Downstate Health Sciences University · USTulane University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe innate immune system is recognized as an essential aspect of COVID-19 pathogenesis. Toll-like receptors (TLRs) are important in inducing antiviral response, triggering downstream production of interferons (IFNs). Certain loss-of-function variants in TLR7 are associated with increased COVID-19 disease severity, and imiquimod (ImiQ) is known to have immunomodulating effects as an agonist of TLR7. Given that topical imiquimod (topImiQ) is indicated for various dermatologic conditions, it is necessary for dermatologists to understand the interplay between innate immunity mechanisms and the potential role of ImiQ in COVID-19, with a particular focus on TLR7. SUMMARY: Our objective was to survey recent peer-reviewed scientific literature in the PubMed database, examine relevant evidence, and elucidate the relationships between IFNs, TLR7, the innate immune system, and topImiQ in the context of COVID-19. Despite limited studies on this topic, current evidence supports the critical role of TLRs in mounting a strong immune response against COVID-19. Of particular interest to dermatologists, topImiQ can result in systemic upregulation of the immune system via activation of TLR7. Key Message: Given the role of TLR7 in the systemic activation of the immune system, ImiQ, as a ligand of the TLR7 receptor, may have potential therapeutic benefit as a topical immunomodulatory treatment for COVID-19.

Indexed as

Immunity, InnateSARS-CoV-2Adjuvants, ImmunologicAdministration, TopicalAnimalsAntiviral AgentsCOVID-19HumansImiquimodInterferonsToll-Like Receptor 7Up-RegulationAdjuvants, ImmunologicAntiviral AgentsImiquimodInterferonsTLR7 protein, humanToll-Like Receptor 7COVID-19ImiquimodInterferonsToll-like receptorsTopical imiquimod

Identifiers

PMID34511591
PMCPMC8450856
OpenAlexW3197134309

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.