Evidence map›Paper›PMID 42220525›Full record

ArticleFrontiers in immunology2026

Comparative analysis of the impact of interferon regulatory factors on basal and induced interferon and interferon stimulated gene expression in human and canine keratinocytes.

Sarah Quinlan, Susan May, Ryan Weeks, Jennifer Luff

Abstract readComparative Study
In one paragraph

Article in Frontiers in immunology, 2026. 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

4 authors.

Sarah QuinlanNorth Carolina State University, Department of Population Health and Pathobiology, Raleigh, NC, United States.
Susan MayNorth Carolina State University, Department of Population Health and Pathobiology, Raleigh, NC, United States.
Ryan WeeksNorth Carolina State University, Department of Population Health and Pathobiology, Raleigh, NC, United States.
Jennifer LuffNorth Carolina State University, Department of Population Health and Pathobiology, Raleigh, NC, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Keratinocytes are key barrier cells able to mount a robust interferon (IFN) antiviral response to defend against infection in the skin. Similar to humans, dogs spontaneously develop skin disorders associated with dysregulation of IFN immunity and can be used as a large animal model to investigate these diseases. One of the critical factors driving IFN regulation are interferon regulatory factors (IRFs). IRFs are crucial in upregulating the antiviral type I or type III IFNs, which then subsequently upregulate hundreds of antiviral effector proteins called interferon stimulated genes (ISGs). Methods: We sought to comparatively analyze how IRF1, 3 and 7 regulate type I and type III IFNs and ISGs using canine and human keratinocyte cultures. To this aim, we stimulated keratinocytes Results: We demonstrated that compared to canine keratinocytes, human keratinocytes express higher basal type I IFN-β and ISGs, induce higher levels of type III IFNs upon stimulation, and overall, express higher IFN and ISG copies. We further showed that IRF regulation of induced IFNs, particularly IRF1, can be species-specific and/or stimulus-specific, and putatively that non-IRF mechanisms likely mediate basal expression of type I IFNs in human keratinocytes and type III IFNs in canine keratinocytes. While both IRF3 and IRF7 are critical for type I and III IFN induction following activation of cytosolic dsDNA and dsRNA receptors, neither can account for differences in the induced type I versus III IFN expression between dog and human, suggesting non-IRF1, 3, or 7 mechanisms underly this regulation. Conclusions: These studies provide support for use of the dog as a model to discern mechanisms underlying high basal type I and ISGs in human keratinocytes, how high basal ISGs can modulate the antiviral response, and uncover non-IRF mediated mechanisms regulating the type I versus type III response in keratinocytes.

Indexed as

Gene Expression RegulationInterferon Regulatory FactorsInterferonsKeratinocytesAnimalsCells, CulturedDogsHumansInterferon Regulatory Factor-3Interferon Regulatory Factor-3Interferon Regulatory FactorsInterferonsdoginterferoninterferon regulatory factorinterferon stimulated genekeratinocyte

Identifiers

PMID42220525
PMCPMC13218971

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Registered trials

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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.