Evidence map›Paper›PMID 41573829›Full record

ArticlebioRxiv : the preprint server for biology2025

Keratinocyte VISTA attenuates UV light-induced skin injury by suppressing cutaneous type I interferon (IFN-I) response.

Zachary T Peters, Lindsay K Mendyka, J'Voughnn Blake, Himanshu B Goswami, Angelique N Cortez, Grace E Crossland, Sicong Shan, Elizabeth C Nowak, Mrinal Sarkar, Johann E Gudjodsson and 10 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

20 authors.

Zachary T PetersDepartment of Microbiology and Immunology, Dartmouth Geisel School of Medicine, Lebanon, NH, USA.ORCID 0000-0003-2447-0691
Lindsay K MendykaDepartment of Microbiology and Immunology, Dartmouth Geisel School of Medicine, Lebanon, NH, USA.
J'Voughnn BlakeDepartment of Microbiology and Immunology, Dartmouth Geisel School of Medicine, Lebanon, NH, USA.
Himanshu B GoswamiDepartment of Microbiology and Immunology, Dartmouth Geisel School of Medicine, Lebanon, NH, USA.
Angelique N CortezDepartment of Microbiology and Immunology, Dartmouth Geisel School of Medicine, Lebanon, NH, USA.
Grace E CrosslandDepartment of Microbiology and Immunology, Dartmouth Geisel School of Medicine, Lebanon, NH, USA.
Sicong ShanDepartment of Microbiology and Immunology, Dartmouth Geisel School of Medicine, Lebanon, NH, USA.
Elizabeth C NowakDepartment of Microbiology and Immunology, Dartmouth Geisel School of Medicine, Lebanon, NH, USA.
Mrinal SarkarDepartment of Dermatology, University of Michigan, Ann Arbor, Michigan, USA.
Johann E GudjodssonDepartment of Dermatology, University of Michigan, Ann Arbor, Michigan, USA.
Christopher M BurnsDepartment of Medicine, Dartmouth Health, DHMC, Lebanon, NH, USA.
Dorothea T BartonDepartment of Dermatology, Dartmouth Health, DHMC, Lebanon, NH, USA.
Bruce R BlazarDepartment of Pediatrics, Division of Blood & Marrow Transplant & Cellular Therapy, University of Minnesota, Minneapolis, MN, USA.
Tyler J CurielDepartment of Medicine, Dartmouth Health, DHMC, Lebanon, NH, USA.
Rodwell MabaeraDepartment of Medicine, Dartmouth Health, DHMC, Lebanon, NH, USA.
Victoria P WerthDepartment of Dermatology, University of Pennsylvania and Corporal Michael J. Crescenz VAMC, Philadelphia, PA, USA.
Andrea KalusDivision of Dermatology, University of Washington School of Medicine, Seattle, WA, USA.
Keith ElkonDivision of Rheumatology, University of Washington School of Medicine, Seattle, WA, USA.
Randolph J NoelleDepartment of Microbiology and Immunology, Dartmouth Geisel School of Medicine, Lebanon, NH, USA.
Sladjana Skopelja-GardnerDepartment of Microbiology and Immunology, Dartmouth Geisel School of Medicine, Lebanon, NH, USA.

Funding

Translational Engineering in Cancer (TEC)P30CA023108 · NCI · DARTMOUTH COLLEGE · PI Fred W Kolling IV · 1985 to 2026
$91.3M
Zhao - Proj 2P20GM130454 · NIGMS · DARTMOUTH COLLEGE · PI MICHAEL L WHITFIELD · 2019 to 2026
$27.2M
IMMUNOBIOLOGY OF MYELOID AND LYMPHOID CELLST32AI007363 · NIAID · DARTMOUTH COLLEGE · PI Claudia V Jakubzick · 1990 to 2026
$9.5M
University of Michigan Skin Biology and Diseases Resource-based CenterP30AR075043 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Johann Eli Gudjonsson · 2019 to 2026
$6.6M
VISTA is a negative checkpoint regulator of innate immunityR01AI148430 · NIAID · DARTMOUTH COLLEGE · PI MABAERA, RODWELL, SKOPELJA-GARDNER, SLADJANA · 2020 to 2024
$4.0M
Exploiting the VISTA Pathway to Prevent Acute GVHD and Control Steroid Refractory DiseaseR01HL155114 · NHLBI · UNIVERSITY OF MINNESOTA · PI BLAZAR, BRUCE R, NOELLE, RANDOLPH J. · 2021 to 2024
$2.7M
The Role of PHF6 in HSC self-renewal and myeloid expansionR01HL155144 · NHLBI · UNIVERSITY OF PENNSYLVANIA · PI PARALKAR, VIKRAM R. · 2021 to 2024
$2.2M
VISTA regulates type I interferon response to ultraviolet lightR21AR079661 · NIAMS · DARTMOUTH-HITCHCOCK CLINIC · PI SKOPELJA-GARDNER, SLADJANA · 2021 to 2021
$384k
Acquisition of the NextSeq2000 Sequencing platform to Increase Next Generation Sequencing Throughput While Reducing Costs at DartmouthS10OD030242 · OD · DARTMOUTH COLLEGE · PI KOLLING IV, FRED W · 2021 to 2021
$321k
10X Genomics Chromium Single-cell Sequencing to Expand Research At DartmouthS10OD025235 · OD · DARTMOUTH COLLEGE · PI TOMLINSON, CRAIG R · 2018 to 2018
$125k
NCI NIH HHS P30 CA023108NHLBI NIH HHS R01 HL155114NHLBI NIH HHS R01 HL155144NIAID NIH HHS R01 AI148430NIAID NIH HHS T32 AI007363NIAMS NIH HHS P30 AR075043NIAMS NIH HHS R21 AR079661NIGMS NIH HHS P20 GM130454NIH HHS S10 OD025235NIH HHS S10 OD030242
6 · The paper itself

Abstract

Persistent production of type I interferons (IFN-Is) is a hallmark of cutaneous lupus erythematosus (CLE). Ultraviolet (UV) light stimulates IFN-I response in the skin and exacerbates CLE. Here, we identify V-type immunoglobulin domain-containing suppressor of T cell activation (VISTA) as a negative regulator of both basal and UV-induced IFN-I responses in the skin and show that VISTA limits skin photosensitivity in an IFN-I-dependent manner, in part through Stimulator of Interferon Genes (STING). Furthermore, we demonstrate a novel role for VISTA in keratinocytes both at steady state and in response to UV light. Conditional deletion of VISTA in epidermal keratinocytes results in >10-fold increase in the basal skin IFN-I score and a heightened UV-induced skin injury score, which is dependent on IFN-I signaling. VISTA-targeting monoclonal antibodies suppress UV-induced IFN-I response in human keratinocytes and in mice expressing human VISTA

Indexed as

Biological SciencesImmunology and InflammationInterferonKeratinocyteLupus

Identifiers

PMID41573829
PMCPMC12822643

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.