Evidence map›Paper›PMID 33717655›Full record

ArticleOncoimmunology2021

Galectin-3 inhibition with belapectin combined with anti-OX40 therapy reprograms the tumor microenvironment to favor anti-tumor immunity.

Elizabeth R Sturgill, Annah S Rolig, Stefanie N Linch, Courtney Mick, Melissa J Kasiewicz, Zhaoyu Sun, Peter G Traber, Harold Shlevin, William L Redmond

Open access · goldAbstract read
In one paragraph

Article in Oncoimmunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.0field-weighted citation impact, top 8% 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

35 citing papers in PubMed, 47 citations in OpenAlex.

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  11. Gal-3 blocks the binding between PD-1 and pembrolizumab.Journal for immunotherapy of cancer · 2024
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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

9 authors at 2 institutions in 2 countries.

Elizabeth R SturgillEarle A. Chiles Research Institute, Providence Cancer Institute, Portland, OR, USA.
Annah S RoligEarle A. Chiles Research Institute, Providence Cancer Institute, Portland, OR, USA.ORCID 0000-0001-7080-4352
Stefanie N LinchEarle A. Chiles Research Institute, Providence Cancer Institute, Portland, OR, USA.
Courtney MickEarle A. Chiles Research Institute, Providence Cancer Institute, Portland, OR, USA.
Melissa J KasiewiczEarle A. Chiles Research Institute, Providence Cancer Institute, Portland, OR, USA.
Zhaoyu SunEarle A. Chiles Research Institute, Providence Cancer Institute, Portland, OR, USA.
Peter G TraberUniversity of Pennsylvania School of Medicine, Philadelphia, PA, USA.
Harold ShlevinGalectin Therapeutics, Norcross, GA, USA.
William L RedmondEarle A. Chiles Research Institute, Providence Cancer Institute, Portland, OR, USA.ORCID 0000-0002-2572-1731
Cancer Institute (WIA) · INUniversity of Pennsylvania · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Treatment with an agonist anti-OX40 antibody (aOX40) boosts anti-tumor immunity by providing costimulation and driving effector T cell responses. However, tumor-induced immune suppression contributes significantly to poor response rates to aOX40 therapy, thus combining aOX40 with other agents that relieve tumor-mediated immune suppression may significantly improve outcomes. Once such target is galectin-3 (Gal-3), which drives tumor-induced immunosuppression by increasing macrophage infiltration and M2 polarization, restricting TCR signaling, and inducing T cell apoptosis. A wide-variety of tumors also upregulate Gal-3, which is associated with poor prognosis. Tumor-bearing (MCA-205 sarcoma, 4T1 mammary carcinoma, TRAMP-C1 prostate adenocarcinoma) mice were treated with a Gal-3 inhibitor (belapectin; GR-MD-02), aOX40, or combination therapy and the extent of tumor growth was determined. The phenotype and function of tumor-infiltrating lymphocytes was determined by flow cytometry, multiplex cytokine assay, and multiplex immunohistochemistry. Gal-3 inhibition synergized with aOX40 to promote tumor regression and increase survival. Specifically, aOX40/belapectin therapy significantly improved survival of tumor-bearing mice through a CD8

Indexed as

Antineoplastic AgentsMyeloid-Derived Suppressor CellsProstatic NeoplasmsAnimalsGalectin 3HumansMaleMiceTumor MicroenvironmentAntineoplastic AgentsGalectin 3CD8-Positive T-Lymphocytescheckpoint Inhibitorcostimulationimmunotherapymyeloid-Derived Suppressor Cellstumor Microenvironment

Identifiers

PMID33717655
PMCPMC7927986
OpenAlexW3135628008

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.