Evidence map›Paper›PMID 36891296›Full record

ReviewFrontiers in immunology2023

VISTA expression and patient selection for immune-based anticancer therapy.

Alexander S Martin, Michael Molloy, Andrey Ugolkov, Reinhard W von Roemeling, Randolph J Noelle, Lionel D Lewis, Melissa Johnson, Laszlo Radvanyi, Robert E Martell

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
9.7field-weighted citation impact, top 2% 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

46 citing papers in PubMed, 42 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Observational
  6. Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Review
  17. Review
  18. Article
  19. Article
  20. 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

9 authors at 6 institutions in 2 countries.

Alexander S MartinDivision of Hematology/Oncology, Tufts Medical Center, Boston, MA, United States.
Michael MolloyImmuNext Inc., Lebanon, NH, United States.
Andrey UgolkovCuris Inc., Lexington, MA, United States.
Reinhard W von RoemelingCuris Inc., Lexington, MA, United States.
Randolph J NoelleImmuNext Inc., Lebanon, NH, United States.
Lionel D LewisDepartment of Microbiology and Immunology, Norris Cotton Cancer Center Geisel School of Medicine at Dartmouth, Lebanon, NH, United States.
Melissa JohnsonSarah Cannon at Tennessee Oncology, Nashville, TN, United States.
Laszlo RadvanyiOntario Institute for Cancer Research, Toronto, ON, Canada.
Robert E MartellDivision of Hematology/Oncology, Tufts Medical Center, Boston, MA, United States.
Curis (United States) · USImmuNext (United States) · USTufts Medical Center · USDartmouth College · USOntario Institute for Cancer Research · CASarah Cannon · US

Funding

CTSA Graduate ProgramTL1TR002546 · NCATS · TUFTS UNIVERSITY BOSTON · PI KENT, DAVID M · 2018 to 2022
$4.2M
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
NCATS NIH HHS TL1 TR002546NHLBI NIH HHS R01 HL155114
6 · The paper itself

Abstract

V-domain Ig suppressor of T-cell activation (VISTA) is a B7 family member that plays key roles in maintaining T cell quiescence and regulation of myeloid cell populations, which together establish it as a novel immunotherapy target for solid tumors. Here we review the growing literature on VISTA expression in relation to various malignancies to better understand the role of VISTA and its interactions with both tumor cells and immune cells expressing other checkpoint molecules within the tumor microenvironment (TME). The biology of VISTA creates several mechanisms to maintain the TME, including supporting the function of myeloid-derived suppressor cells, regulating natural killer cell activation, supporting the survival of regulatory T cells, limiting antigen presentation on antigen-presenting cells and maintaining T cells in a quiescent state. Understanding these mechanisms is an important foundation of rational patient selection for anti-VISTA therapy. We provide a general framework to describe distinct patterns of VISTA expression in correlation with other known predictive immunotherapy biomarkers (programmed cell death ligand 1 and tumor-infiltrating lymphocytes) across solid tumors to facilitate investigation of the most efficacious TMEs for VISTA-targeted treatment as a single agent and/or in combination with anti-programmed death 1/anti-cytotoxic T lymphocyte antigen-4 therapies.

Indexed as

B7 AntigensNeoplasmsBiomarkersHumansPatient SelectionT-Lymphocytes, RegulatoryTumor MicroenvironmentB7 AntigensBiomarkersVSIR protein, humanbiomarkerscancercancer immunotherapyimmune checkpointtumor immunitytumor microenvironmentVISTA

Identifiers

PMID36891296
PMCPMC9986543
OpenAlexW4321375958

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.