Evidence map›Paper›PMID 40574311›Full record

ArticleJournal of immunology (Baltimore, Md. : 1950)2025

The role of VISTA engagement in limiting neutrophil-mediated inflammation.

Elizabeth C Nowak, Jiannan Li, Zachary T Peters, Lindsay K Mendyka, Mohamed A ElTanbouly, Wilson L Davis, Petra Sergent, J Louise Lines, Nicole C Smits, Rodwell Mabaera and 8 more

Abstract read
In one paragraph

Article in Journal of immunology (Baltimore, Md. : 1950), 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

18 authors.

Elizabeth C NowakDepartment of Microbiology and Immunology, Dartmouth Cancer Center, Geisel School of Medicine at Dartmouth, Lebanon, NH, United States.
Jiannan LiDepartment of Microbiology and Immunology, Dartmouth Cancer Center, Geisel School of Medicine at Dartmouth, Lebanon, NH, United States.
Zachary T PetersDepartment of Microbiology and Immunology, Dartmouth Cancer Center, Geisel School of Medicine at Dartmouth, Lebanon, NH, United States.
Lindsay K MendykaDepartment of Microbiology and Immunology, Dartmouth Cancer Center, Geisel School of Medicine at Dartmouth, Lebanon, NH, United States.
Mohamed A ElTanboulyDepartment of Microbiology and Immunology, Dartmouth Cancer Center, Geisel School of Medicine at Dartmouth, Lebanon, NH, United States.
Wilson L DavisDepartment of Microbiology and Immunology, Dartmouth Cancer Center, Geisel School of Medicine at Dartmouth, Lebanon, NH, United States.
Petra SergentDepartment of Microbiology and Immunology, Dartmouth Cancer Center, Geisel School of Medicine at Dartmouth, Lebanon, NH, United States.
J Louise LinesDepartment of Microbiology and Immunology, Dartmouth Cancer Center, Geisel School of Medicine at Dartmouth, Lebanon, NH, United States.
Nicole C SmitsDepartment of Microbiology and Immunology, Dartmouth Cancer Center, Geisel School of Medicine at Dartmouth, Lebanon, NH, United States.
Rodwell MabaeraDepartment of Microbiology and Immunology, Dartmouth Cancer Center, Geisel School of Medicine at Dartmouth, Lebanon, NH, United States.
Shibani RajannaImmuNext Corporation, Lebanon, NH, United States.
Catherine CarriereImmuNext Corporation, Lebanon, NH, United States.
Brent KoehnDepartment of Pediatrics, Division of Bone Marrow & Blood Transplant & Cellular Therapy, University of Minnesota, Minneapolis, MN, United States.
Jeremy AllredDepartment of Pediatrics, Division of Bone Marrow & Blood Transplant & Cellular Therapy, University of Minnesota, Minneapolis, MN, United States.
Bruce R BlazarDepartment of Pediatrics, Division of Bone Marrow & Blood Transplant & Cellular Therapy, University of Minnesota, Minneapolis, MN, United States.ORCID 0000-0002-9608-9841
Christopher M BurnsDepartment of Medicine, Dartmouth-Hitchcock Medical Center, Lebanon, NH, United States.
Randolph J NoelleDepartment of Microbiology and Immunology, Dartmouth Cancer Center, Geisel School of Medicine at Dartmouth, Lebanon, NH, United States.
Sladjana Skopelja-GardnerDepartment of Microbiology and Immunology, Dartmouth Cancer Center, Geisel School of Medicine at Dartmouth, Lebanon, NH, United States.

Funding

Translational Engineering in Cancer (TEC)P30CA023108 · NCI · DARTMOUTH COLLEGE · PI Steven D Leach · 1985 to 2026
$91.3M
In Vivo Prevention of Murine GVHDR37AI034495 · NIAID · UNIVERSITY OF MINNESOTA · PI Bruce R Blazar · 2017 to 2026
$5.4M
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
VISTA regulates type I interferon response to ultraviolet lightR21AR079661 · NIAMS · DARTMOUTH-HITCHCOCK CLINIC · PI SKOPELJA-GARDNER, SLADJANA · 2021 to 2021
$384k
2022 Lupus Research Alliance Lupus Innovation AwardCongressionally Directed Medical Research Programs Lupus Research Program W81XWH2110889Dartmouth's Immune Monitoring and Flow Cytometry ResourceNational Cancer Institute Cancer 5P30CA023108NCI NIH HHS P30 CA023108NHLBI NIH HHS R01 HL155114NIAID NIH HHS R01 AI148430NIAID NIH HHS R37 AI034495NIAMS NIH HHS R21 AR079661NIAMS NIH HHS R21 AR079661-01NIH
6 · The paper itself

Abstract

A growing body of evidence suggests that the immune checkpoint inhibitory receptor VISTA plays a central role in the regulation of innate immunity in the settings of inflammatory diseases and cancer. Neutrophils are among the cells that have the highest membrane density of surface VISTA. In this study, targeting VISTA on neutrophils with a monoclonal antibody resulted in a striking reduction in their lipopolysaccharide (LPS)- and chemokine-induced peripheral accumulation but did not reduce neutrophil levels at steady state. Fc receptor engagement and macrophages were required for the effects of anti-VISTA antibody on neutrophils. Concomitant with reduced peripheral neutrophil numbers, targeting VISTA increased neutrophil clearance by macrophages in the liver. In a murine model of neutrophil-mediated arthritis, anti-VISTA antibody treatment ameliorated disease severity, which was associated with reduced myeloperoxidase activity in the joints. These studies identify a novel therapeutic opportunity for targeting VISTA to control neutrophil-mediated inflammation and tissue injury.

Indexed as

Arthritis, ExperimentalB7 AntigensInflammationNeutrophilsAnimalsAntibodies, MonoclonalDisease Models, AnimalHumansLipopolysaccharidesMacrophagesMembrane ProteinsMiceMice, Inbred C57BLAntibodies, MonoclonalB7 AntigensLipopolysaccharidesMembrane ProteinsVsir protein, mouseimmune checkpointinflammationneutrophilsVISTA

Identifiers

PMID40574311
PMCPMC12336919

What OpenQuestion holds

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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.