Evidence map›Paper›PMID 41445728›Full record

ArticleFrontiers in immunology2025

Modulation of

Estíbaliz Alegría-Carrasco, Marta Jaén-Castaño, Pablo Delgado-Wicke, Nelly D Zurita-Cruz, Nuria Montes, Emilia Roy-Vallejo, Sara Fernández de Córdoba-Oñate, Ana Nicolao-Gómez, Rosa Carracedo-Rodríguez, Ana Marcos-Jiménez and 3 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

13 authors.

Estíbaliz Alegría-CarrascoMolecular Biology Unit, La Princesa University Hospital and Health Research Institute (IIS-Princesa), Madrid, Spain.
Marta Jaén-CastañoMolecular Biology Unit, La Princesa University Hospital and Health Research Institute (IIS-Princesa), Madrid, Spain.
Pablo Delgado-WickeMolecular Biology Unit, La Princesa University Hospital and Health Research Institute (IIS-Princesa), Madrid, Spain.
Nelly D Zurita-CruzMicrobiology Department, La Princesa University Hospital (IIS-Princesa), Madrid, Spain.
Nuria MontesRheumatology Department, La Princesa University Hospital (IIS-Princesa), Madrid, Spain.
Emilia Roy-VallejoInternal Medicine Department, La Princesa University Hospital (IIS-Princesa), Madrid, Spain.
Sara Fernández de Córdoba-OñateRheumatology Department, La Princesa University Hospital (IIS-Princesa), Madrid, Spain.
Ana Nicolao-GómezMolecular Biology Unit, La Princesa University Hospital and Health Research Institute (IIS-Princesa), Madrid, Spain.
Rosa Carracedo-RodríguezMolecular Biology Unit, La Princesa University Hospital and Health Research Institute (IIS-Princesa), Madrid, Spain.
Ana Marcos-JiménezImmunology Department, La Princesa University Hospital (IIS-Princesa), Madrid, Spain.
Laura Cardeñoso-DomingoMicrobiology Department, La Princesa University Hospital (IIS-Princesa), Madrid, Spain.
Isidoro González-Álvaro *Rheumatology Department, La Princesa University Hospital (IIS-Princesa), Madrid, Spain.
Elena Fernández-Ruiz *Molecular Biology Unit, La Princesa University Hospital and Health Research Institute (IIS-Princesa), Madrid, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The host response to SARS-CoV-2 depends on multiple factors including age, gender, underlying diseases and genetic background. Viral sensing and activation of the interferon signaling pathway in the early antiviral response could affect disease outcome. This study evaluated gene expression of Toll-like receptor 7 ( Methods: Demographic and clinical variables were obtained from 157 COVID-19 patients. Peripheral blood mononuclear cells were used for genotyping and gene expression determination, and plasma for viremia detection, by qPCR and digital PCR, respectively. Gene expression was analyzed using Generalized Linear Mixed Models nested by patient. First, univariate analyses determined which variables were significantly associated with gene expression. Next, multivariate models were built with these variables, following the backward method. Results: Conclusions: Low

Indexed as

2',5'-Oligoadenylate SynthetaseCOVID-19SARS-CoV-2Toll-Like Receptor 7TYK2 KinaseAdultAgedFemaleHumansLeukocytes, MononuclearMaleMiddle AgedSeverity of Illness Index2',5'-Oligoadenylate SynthetaseOAS1 protein, humanTLR7 protein, humanToll-Like Receptor 7TYK2 KinaseTYK2 protein, humanCOVID-19longitudinal studyOAS1SARS-CoV-2severityTLR7TYK2viremia

Identifiers

PMID41445728
PMCPMC12722446

What OpenQuestion holds

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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.