Evidence map›Paper›PMID 35832809›Full record

ReviewFrontiers in microbiology2022

Toll-Like Receptor Signaling in Severe Acute Respiratory Syndrome Coronavirus 2-Induced Innate Immune Responses and the Potential Application Value of Toll-Like Receptor Immunomodulators in Patients With Coronavirus Disease 2019.

Jiayu Dai, Yibo Wang, Hongrui Wang, Ziyuan Gao, Ying Wang, Mingli Fang, Shuyou Shi, Peng Zhang, Hua Wang, Yingying Su and 1 more

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in microbiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 1 pooled it
4.1field-weighted citation impact, top 4% 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

31 citing papers in PubMed, 1 synthesis or guideline pooled it, 44 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. COVID-19, the disease that changed the world.Medicine and pharmacy reports · 2026
    Review
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  7. Article
  8. Review
  9. Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Variants rs3804099 and rs3804100 in theInternational journal of molecular sciences · 2024
    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

11 authors at 3 institutions in 1 country.

Jiayu DaiDepartment of Molecular Biology, College of Basic Medical Sciences, Jilin University, Changchun, China.
Yibo WangDepartment of Molecular Biology, College of Basic Medical Sciences, Jilin University, Changchun, China.
Hongrui WangDepartment of Molecular Biology, College of Basic Medical Sciences, Jilin University, Changchun, China.
Ziyuan GaoDepartment of Molecular Biology, College of Basic Medical Sciences, Jilin University, Changchun, China.
Ying WangDepartment of Molecular Biology, College of Basic Medical Sciences, Jilin University, Changchun, China.
Mingli FangDepartment of Molecular Biology, College of Basic Medical Sciences, Jilin University, Changchun, China.
Shuyou ShiDepartment of Molecular Biology, College of Basic Medical Sciences, Jilin University, Changchun, China.
Peng ZhangDepartment of Thoracic Surgery, The First Affiliated Hospital of Jilin University, Changchun, China.
Hua WangDepartment of Molecular Biology, College of Basic Medical Sciences, Jilin University, Changchun, China.
Yingying SuDepartment of Anatomy, College of Basic Medical Sciences, Jilin University, Jilin, China.
Ming YangDepartment of Molecular Biology, College of Basic Medical Sciences, Jilin University, Changchun, China.
Jilin Medical University · CNJilin University · CNFirst Hospital of Jilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Toll-like receptors (TLRs) are key sensors that recognize the pathogen-associated molecular patterns (PAMPs) of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) to activate innate immune response to clear the invading virus. However, dysregulated immune responses may elicit the overproduction of proinflammatory cytokines and chemokines, resulting in the enhancement of immune-mediated pathology. Therefore, a proper understanding of the interaction between SARS-CoV-2 and TLR-induced immune responses is very important for the development of effective preventive and therapeutic strategies. In this review, we discuss the recognition of SARS-CoV-2 components by TLRs and the downstream signaling pathways that are activated, as well as the dual role of TLRs in regulating antiviral effects and excessive inflammatory responses in patients with coronavirus disease 2019 (COVID-19). In addition, this article describes recent progress in the development of TLR immunomodulators including the agonists and antagonists, as vaccine adjuvants or agents used to treat hyperinflammatory responses during SARS-CoV-2 infection.

Indexed as

COVID-19immunomodulatorinnate immune responseSARS-CoV-2Toll-like receptor

Identifiers

PMID35832809
PMCPMC9271922
OpenAlexW4283585951

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.