Evidence map›Paper›PMID 35891331›Full record

ReviewViruses2022

Coronaviral Infection and Interferon Response: The Virus-Host Arms Race and COVID-19.

Qi Liu, Sensen Chi, Kostyantyn Dmytruk, Olena Dmytruk, Shuai Tan

Open access · goldAbstract readReview
In one paragraph

Review in Viruses, 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
1.9field-weighted citation impact, top 13% 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, 20 citations in OpenAlex.

  1. Article
  2. Nanocarrier-based immunotherapy for viral diseases.International journal of pharmaceutics: X · 2025
    Review
  3. Review
  4. Article
  5. Review
  6. The Immune Response ofInternational journal of molecular sciences · 2024
    Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Editorial: Pattern-recognition receptors: Genetics, immunity, pathology.Frontiers in cellular and infection microbiology · 2022
    Article
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

5 authors at 3 institutions in 4 countries.

Qi LiuDepartment of Immunology, School of Basic Medicine, Chongqing Medical University, Chongqing 400010, China.
Sensen ChiDepartment of Immunology, School of Basic Medicine, Chongqing Medical University, Chongqing 400010, China.
Kostyantyn DmytrukDepartment of Molecular Genetics and Biotechnology, Institute of Cell Biology, National Academy of Sciences of Ukraine, 79005 Lviv, Ukraine.
Olena DmytrukDepartment of Molecular Genetics and Biotechnology, Institute of Cell Biology, National Academy of Sciences of Ukraine, 79005 Lviv, Ukraine.
Shuai TanDepartment of Immunology, School of Basic Medicine, Chongqing Medical University, Chongqing 400010, China.
Chongqing Medical University · CNNational Academy of Sciences of Ukraine · UAThe University of Texas Southwestern Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The recent pandemic caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has resulted in unprecedented morbidity and mortality worldwide. The host cells use a number of pattern recognition receptors (PRRs) for early detection of coronavirus infection, and timely interferon secretion is highly effective against SARS-CoV-2 infection. However, the virus has developed many strategies to delay interferon secretion and disarm cellular defense by intervening in interferon-associated signaling pathways on multiple levels. As a result, some COVID-19 patients suffered dramatic susceptibility to SARS-CoV-2 infection, while another part of the population showed only mild or no symptoms. One hypothesis suggests that functional differences in innate immune integrity could be the key to such variability. This review tries to decipher possible interactions between SARS-CoV-2 proteins and human antiviral interferon sensors. We found that SARS-CoV-2 actively interacts with PRR sensors and antiviral pathways by avoiding interferon suppression, which could result in severe COVID-19 pathogenesis. Finally, we summarize data on available antiviral pharmaceutical options that have shown potential to reduce COVID-19 morbidity and mortality in recent clinical trials.

Indexed as

COVID-19 Drug TreatmentAntiviral AgentsHumansImmunity, InnateInterferonsPandemicsSARS-CoV-2Antiviral AgentsInterferonsantiviral drugCOVID-19innate immuneinterferonpattern-recognition receptorPRRSARS-CoV-2

Identifiers

PMID35891331
PMCPMC9325157
OpenAlexW4283360029

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.