Evidence map›Paper›PMID 25691328›Full record

ArticleCancer immunology research2015

Galectin-3 Shapes Antitumor Immune Responses by Suppressing CD8+ T Cells via LAG-3 and Inhibiting Expansion of Plasmacytoid Dendritic Cells.

Theodore Kouo, Lanqing Huang, Alexandra B Pucsek, Minwei Cao, Sara Solt, Todd Armstrong, Elizabeth Jaffee

Open access · bronzeAbstract read
In one paragraph

Article in Cancer immunology research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 335 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
335citing papers in PubMed, 1 pooled it
10.7field-weighted citation impact, top 1% 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

335 citing papers in PubMed, 1 synthesis or guideline pooled it, 512 citations in OpenAlex.

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  13. Advances in Cancer Immunotherapy for Solid Tumors.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
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275 more citing papers are in PubMed but not listed here.

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

7 authors at 2 institutions in 1 country.

Theodore KouoDepartment of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland. tkouo1@jhmi.edu ejaffee@jhmi.edu.
Lanqing HuangDepartment of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Alexandra B PucsekDepartment of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Minwei CaoDepartment of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Sara SoltDepartment of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Todd ArmstrongDepartment of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Elizabeth JaffeeDepartment of Oncology, Johns Hopkins University School of Medicine, Baltimore, Maryland. tkouo1@jhmi.edu ejaffee@jhmi.edu.
Johns Hopkins University · USJohns Hopkins Medicine · US

Funding

Translational Research Central ServicesP30CA006973 · NCI · JOHNS HOPKINS UNIVERSITY · PI Rosalie Wollett · 1985 to 2026
$208.6M
Tumor Antigens for Individual Signatures and TherapyP50CA062924 · NCI · JOHNS HOPKINS UNIVERSITY · PI LENNON, ANNE MARIE · 1993 to 2022
$54.6M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM007309 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI COX, ANDREA L · 1985 to 2019
$43.2M
CELLULAR &MOLECULAR MECH OF INFLAMMATORY REACTIONST32AI007247 · NIAID · JOHNS HOPKINS UNIVERSITY · PI Joel L Pomerantz · 1985 to 2026
$10.2M
(PQB-3) Driver gene-induced inflammation in pancreatic cancer developmentR01CA184926 · NCI · JOHNS HOPKINS UNIVERSITY · PI JAFFEE, ELIZABETH M. · 2014 to 2017
$3.1M
NCI NIH HHS P30 CA006973NCI NIH HHS P50 CA062924NCI NIH HHS P50CA062924NCI NIH HHS R01 CA184926NCI NIH HHS R01CA184926NIAID NIH HHS T32 AI007247NIGMS NIH HHS T32 GM007309
6 · The paper itself

Abstract

Galectin-3 is a 31-kDa lectin that modulates T-cell responses through several mechanisms, including apoptosis, T-cell receptor (TCR) cross-linking, and TCR downregulation. We found that patients with pancreatic ductal adenocarcinoma (PDA) who responded to a granulocyte-macrophage colony-stimulating factor-secreting allogeneic PDA vaccine developed neutralizing antibodies to galectin-3 after immunization. We show that galectin-3 binds activated antigen-committed CD8(+) T cells only in the tumor microenvironment. Galectin-3-deficient mice exhibit improved CD8(+) T-cell effector function and increased expression of several inflammatory genes. Galectin-3 binds to LAG-3, and LAG-3 expression is necessary for galectin-3-mediated suppression of CD8(+) T cells in vitro. Lastly, galectin-3-deficient mice have elevated levels of circulating plasmacytoid dendritic cells, which are superior to conventional dendritic cells in activating CD8(+) T cells. Thus, inhibiting galectin-3 in conjunction with CD8(+) T-cell-directed immunotherapies should enhance the tumor-specific immune response.

Indexed as

AnimalsAntigens, CDCancer VaccinesCarcinoma, Pancreatic DuctalCD8-Positive T-LymphocytesCell DifferentiationDendritic CellsFemaleGalectin 3HumansImmune ToleranceImmunophenotypingInterferon-gammaLymphocyte ActivationLymphocyte Activation Gene 3 ProteinLymphocytes, Tumor-InfiltratingAntigens, CDCancer VaccinesGalectin 3Interferon-gammaLymphocyte Activation Gene 3 Protein

Identifiers

PMID25691328
PMCPMC4390508
OpenAlexW2117552772

What OpenQuestion holds

Textmetadata
LicenceTDM
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.