Evidence map›Paper›PMID 40316725›Full record

ArticleBritish journal of cancer2025

Macrophages suppress CD8 + T cell cytotoxic function in triple negative breast cancer via VISTA.

Maidinaimu Abudula, Yuliana Astuti, Meirion Raymant, Vijay Sharma, Michael C Schmid, Ainhoa Mielgo

Abstract read
In one paragraph

Article in British journal of cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Eutopic Endometrium Immune Changes Involved in Development and Progression of Endometriosis: A Review.Medical science monitor : international medical journal of experimental and clinical research · 2026
    Review
  6. Review
  7. Review
  8. 3D bioprinting innovations: a new frontier in breast cancer research.Medical oncology (Northwood, London, England) · 2025
    Review
  9. Review
  10. Review
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

6 authors.

Maidinaimu AbudulaDepartment of Molecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, UK.
Yuliana AstutiDepartment of Molecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, UK.
Meirion RaymantDepartment of Molecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, UK.
Vijay SharmaSchool of Medicine and Department of Molecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, UK.
Michael C SchmidDepartment of Molecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, UK.
Ainhoa MielgoDepartment of Molecular and Clinical Cancer Medicine, University of Liverpool, Liverpool, UK. amielgo@liverpool.ac.uk.ORCID http://orcid.org/0000-0002-4159-5931

Funding

Society for Epidemiologic Research Doctoral Dissertation WorkshopR13TR002021 · NCATS · BOSTON UNIVERSITY MEDICAL CAMPUS · PI HARLOW, BERNARD L · 2017 to 2018
$46k
Cancer Research UK (CRUK) A25607, A26978NCATS NIH HHS R13 TR002021North West Cancer Research Fund (NWCR) CR1194, TR2021.03RCUK | Medical Research Council (MRC) MR/P018920/1Wellcome TrustWellcome Trust (Wellcome) 102521/Z/13/Z
6 · The paper itself

Abstract

backgroundImmunotherapy targeting negative immune checkpoint regulators to enhance the anti-tumour immune response holds promise in the treatment of TNBC. V-domain Ig suppressor of T-cell activation (VISTA) is an immune checkpoint molecule, known to be upregulated and involved in modulating tumour immunity in TNBC. However, how VISTA affects immune response and its therapeutic potential in TNBC remains unclear.

methodHere, we examined VISTA expression and cellular distribution in TNBC patients' samples and pre-clinical TNBC mouse model. Functional assays were performed to assess the impact of VISTA blockade on macrophage phenotypes, CD8 + T cell infiltration and activation, and overall anti-tumour immune response.

resultsIn this study we show that VISTA expression levels are increased in TNBC patients' samples and pre-clinical mouse models compared to non-involved breast tissue and VISTA is mainly expressed on tumour infiltrating macrophages and neutrophils. Blocking VISTA reverts macrophages immunosuppressive phenotypes, increases CD8 + T cell infiltration and activation, and enhances an anti-tumour immune response. Mechanistically, we show that neutralising VISTA on macrophages enhances their immune-stimulatory functions and inhibits the suppressive effect of macrophages on CD8 + T cells activation.

conclusionThese findings provide the rationale for the development of anti-VISTA targeting strategies in the treatment of TNBC.

Indexed as

B7 AntigensCD8-Positive T-LymphocytesMacrophagesMembrane ProteinsTriple Negative Breast NeoplasmsAnimalsCell Line, TumorFemaleHumansMiceB7 AntigensMembrane ProteinsVSIR protein, human

Identifiers

PMID40316725
PMCPMC12238233

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.