Evidence map›Paper›PMID 37795437›Full record

ReviewFrontiers in oncology2023

Clinical and research updates on the VISTA immune checkpoint: immuno-oncology themes and highlights.

Randolph J Noelle, J Louise Lines, Lionel D Lewis, Robert E Martell, Thierry Guillaudeux, Sam W Lee, Kathleen M Mahoney, Matthew D Vesely, Jerome Boyd-Kirkup, Dhanya K Nambiar and 1 more

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
6.7field-weighted citation impact, top 3% of its field
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

25 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Review
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  4. Article
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  6. Current and future immunotherapies for NSCLC.Journal of hematology & oncology · 2026
    Review
  7. Article
  8. Article
  9. Review
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  11. Review
  12. Article
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  14. Article
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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

11 authors at 8 institutions in 2 countries.

Randolph J NoelleImmuNext Inc., Lebanon, NH, United States.
J Louise LinesDepartment of Microbiology and Immunology, Dartmouth Cancer Center, Geisel School of Medicine at Dartmouth, Hanover, NH, United States.
Lionel D LewisSection of Clinical Pharmacology, Department of Medicine, Geisel School of Medicine at Dartmouth and Dartmouth Cancer Center, Hanover, NH, United States.
Robert E MartellCuris, Inc., Lexington, MA, United States.
Thierry GuillaudeuxKineta Inc., Seattle, WA, United States.
Sam W LeeYale University School of Medicine, New Haven, CT, United States.
Kathleen M MahoneyDepartment of Medical, Division of Medical Oncology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, United States.
Matthew D VeselyDepartment of Dermatology, Yale School of Medicine, New Haven, CT, United States.
Jerome Boyd-KirkupHummingbird Bioscience, Houston, TX, United States.
Dhanya K NambiarDepartment of Radiation Oncology, Stanford School of Medicine, Stanford, CA, United States.
Andrew M ScottOlivia Newton-John Cancer Research Institute and School of Cancer Medicine, La Trobe University, Melbourne, VIC, Australia.
Dartmouth Cancer CenterYale University · USCuris (United States) · USDana-Farber Cancer Institute · USDartmouth College · USKineta (United States) · USOlivia Newton-John Cancer Wellness & Research Centre · AUStanford Medicine · US

Funding

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
NHLBI NIH HHS R01 HL155114
6 · The paper itself

Abstract

Immune checkpoints limit the activation of the immune system and serve an important homeostatic function but can also restrict immune responses against tumors. Inhibition of specific immune checkpoint proteins such as the B7:CD28 family members programmed cell death protein-1 (PD-1) and cytotoxic T-lymphocyte antigen-4 (CTLA-4) has transformed the treatment of various cancers by promoting the anti-tumor activation of immune cells. In contrast to these effects, the V-domain immunoglobulin suppressor of T-cell activation (VISTA) regulates the steady state of the resting immune system and promotes homeostasis by mechanisms distinct from PD-1 and CTLA-4. The effects of VISTA blockade have been shown to include a decrease in myeloid suppression coupled with proinflammatory changes by mechanisms that are separate and distinct from other immune checkpoint proteins; in some preclinical studies these immune effects appear synergistic. Given the potential benefits of VISTA blockade in the context of cancer therapy, the second Annual VISTA Symposium was convened virtually on September 23, 2022, to review new research from investigators and immuno-oncology experts. Discussions in the meeting extended the knowledge of VISTA biology and the effects of VISTA inhibition, particularly on cells of the myeloid lineage and resting T cells, as three candidate anti-VISTA antibodies are in, or nearing, clinical development.

Indexed as

checkpoint inhibitors (ICIs)immune checkpointimmuno-oncology (IO)immunotherapymyeloidPD-1VISTA

Identifiers

PMID37795437
PMCPMC10547146
OpenAlexW4386835106

What OpenQuestion holds

Textmetadata
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.