Evidence map›Paper›PMID 38707772›Full record

ArticleFrontiers in lupus2024

A Critical Role for IFN-β Signaling for IFN-κ Induction in Keratinocytes.

Bin Xu, Jon Musai, Yee Sun Tan, Grace A Hile, William R Swindell, Benjamin Klein, J Tingting Qin, Mrinal K Sarkar, Johann E Gudjonsson, J Michelle Kahlenberg

Abstract read
In one paragraph

Article in Frontiers in lupus, 2024. 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
–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

9 citing papers in PubMed.

  1. Article
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  3. Role of E5 from HPV16 in the Evasion of the Immune Response.International journal of molecular sciences · 2026
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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

10 authors.

Bin XuDivision of Rheumatology, Department of Internal Medicine, University of Michigan, Ann Arbor.
Jon MusaiDivision of Rheumatology, Department of Internal Medicine, University of Michigan, Ann Arbor.
Yee Sun TanDivision of Rheumatology, Department of Internal Medicine, University of Michigan, Ann Arbor.
Grace A HileDepartment of Dermatology, University of Michigan, Ann Arbor, Michigan.
William R SwindellUniversity of Texas Southwestern Medical Center, Department of Internal Medicine, Dallas, Texas, 75390-9175.
Benjamin KleinDivision of Rheumatology, Department of Internal Medicine, University of Michigan, Ann Arbor.
J Tingting QinDepartment of Computational Medicine and Bioinformatics, University of Michigan Medical School, Ann Arbor, Michigan, USA.
Mrinal K SarkarDepartment of Dermatology, University of Michigan, Ann Arbor, Michigan.
Johann E GudjonssonDepartment of Dermatology, University of Michigan, Ann Arbor, Michigan.
J Michelle KahlenbergDivision of Rheumatology, Department of Internal Medicine, University of Michigan, Ann Arbor.

Funding

University of Michigan Skin Biology and Diseases Resource-based CenterP30AR075043 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ANDRZEJ A. DLUGOSZ · 2019 to 2026
$6.6M
Characterization of Interferon Kappa as a Novel Target in Cutaneous LupusR01AR071384 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Joanne Michelle Kahlenberg · 2017 to 2026
$3.6M
Linking Disease Mechanisms and Outcomes in Rheumatic DiseasesK24AR076975 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Joanne Michelle Kahlenberg · 2020 to 2026
$910k
NIAMS NIH HHS K24 AR076975NIAMS NIH HHS P30 AR075043NIAMS NIH HHS R01 AR071384
6 · The paper itself

Abstract

Background/Purpose: Cutaneous lupus erythematosus (CLE) affects up to 70% of patients with systemic lupus erythematosus (SLE), and type I interferons (IFNs) are important promoters of SLE and CLE. Our previous work identified IFN-kappa (IFN-κ), a keratinocyte-produced type I IFN, as upregulated in non-lesional and lesional lupus skin and as a critical regulator for enhanced UVB-mediated cell death in SLE keratinocytes. Importantly, the molecular mechanisms governing regulation of IFN-κ expression have been relatively unexplored. Thus, this study sought to identify critical regulators of IFN-κ and identified a novel role for IFN-beta (IFN-β). Methods: Human N/TERT keratinocytes were treated with the RNA mimic poly (I:C) or 50 mJ/cm Results: Time courses of poly(I:C) and UVB treatment revealed a differential expression of Conclusion: Collectively, our work describes a novel mechanistic paradigm in keratinocytes in which initial IFN-κ induction in response to poly(I:C) and UVB is IFNβ1-dependent, thus describing

Identifiers

PMID38707772
PMCPMC11065136

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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.