Evidence map›Paper›PMID 36142620›Full record

ReviewInternational journal of molecular sciences2022

Toll-like Receptor Mediation in SARS-CoV-2: A Therapeutic Approach.

Abdul Manan, Rameez Hassan Pirzada, Muhammad Haseeb, Sangdun Choi

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.7field-weighted citation impact, top 14% 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

9 citing papers in PubMed, 18 citations in OpenAlex.

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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

4 authors at 1 institution in 1 country.

Abdul MananDepartment of Molecular Science and Technology, Ajou University, Suwon 16499, Korea.
Rameez Hassan PirzadaDepartment of Molecular Science and Technology, Ajou University, Suwon 16499, Korea.
Muhammad HaseebDepartment of Molecular Science and Technology, Ajou University, Suwon 16499, Korea.ORCID 0000-0003-1224-8276
Sangdun ChoiDepartment of Molecular Science and Technology, Ajou University, Suwon 16499, Korea.ORCID 0000-0001-5920-7848
Ajou University · KR

Funding

Ministry of Science and ICT, Ministry of Trade, Industry, and Energy, and Ministry of Health and Welfare HN21C1058National Research Foundation of Korea NRF-2022M3A9G1014520, 2019M3D1A1078940, and 2019R1A6A1A11051471
6 · The paper itself

Abstract

The innate immune system facilitates defense mechanisms against pathogen invasion and cell damage. Toll-like receptors (TLRs) assist in the activation of the innate immune system by binding to pathogenic ligands. This leads to the generation of intracellular signaling cascades including the biosynthesis of molecular mediators. TLRs on cell membranes are adept at recognizing viral components. Viruses can modulate the innate immune response with the help of proteins and RNAs that downregulate or upregulate the expression of various TLRs. In the case of COVID-19, molecular modulators such as type 1 interferons interfere with signaling pathways in the host cells, leading to an inflammatory response. Coronaviruses are responsible for an enhanced immune signature of inflammatory chemokines and cytokines. TLRs have been employed as therapeutic agents in viral infections as numerous antiviral Food and Drug Administration-approved drugs are TLR agonists. This review highlights the therapeutic approaches associated with SARS-CoV-2 and the TLRs involved in COVID-19 infection.

Indexed as

COVID-19 Drug TreatmentInterferon Type IAntiviral AgentsChemokinesCytokinesHumansImmunity, InnateLigandsSARS-CoV-2Toll-Like ReceptorsAntiviral AgentsChemokinesCytokinesInterferon Type ILigandsToll-Like Receptorsantiviralimmune systeminflammationSARS-CoV-2TLR

Identifiers

PMID36142620
PMCPMC9502216
OpenAlexW4295926547

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.