Evidence map›Paper›PMID 34367736›Full record

ArticleOncoimmunology2021

Inhibition of arginase modulates T-cell response in the tumor microenvironment of lung carcinoma.

Anna Sosnowska, Justyna Chlebowska-Tuz, Pawel Matryba, Zofia Pilch, Alan Greig, Artur Wolny, Tomasz M Grzywa, Zuzanna Rydzynska, Olga Sokolowska, Tomasz P Rygiel and 5 more

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 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
6.6field-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

69 citing papers in PubMed, 73 citations in OpenAlex.

  1. Review
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  20. Metabolic Control of Immunity-Unveiling Neutrophil Mechanisms.Advances in experimental medicine and biology · 2026
    Review

9 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

15 authors at 4 institutions in 2 countries.

Anna SosnowskaDepartment of Immunology, Medical University of Warsaw, Warsaw, Poland.
Justyna Chlebowska-TuzDepartment of Immunology, Medical University of Warsaw, Warsaw, Poland.
Pawel MatrybaDepartment of Immunology, Medical University of Warsaw, Warsaw, Poland.
Zofia PilchDepartment of Immunology, Medical University of Warsaw, Warsaw, Poland.
Alan GreigDepartment of Cell and Developmental Biology, Division of Biosciences, University College London, London, UK.
Artur WolnyLaboratory of Imaging Tissue Structure and Function, Nencki Institute of Experimental Biology of Polish Academy of Sciences, Warsaw, Poland.
Tomasz M GrzywaDepartment of Immunology, Medical University of Warsaw, Warsaw, Poland.
Zuzanna RydzynskaDepartment of Immunology, Medical University of Warsaw, Warsaw, Poland.
Olga SokolowskaPostgraduate School of Molecular Medicine, Medical University of Warsaw, Warsaw, Poland.
Tomasz P RygielDepartment of Immunology, Medical University of Warsaw, Warsaw, Poland.
Marcin GrzybowskiOncoArendi Therapeutics, Warsaw, Poland.
Paulina StanczakOncoArendi Therapeutics, Warsaw, Poland.
Roman BlaszczykOncoArendi Therapeutics, Warsaw, Poland.
Dominika NowisDepartment of Immunology, Medical University of Warsaw, Warsaw, Poland.ORCID 0000-0003-2748-9523
Jakub GolabDepartment of Immunology, Medical University of Warsaw, Warsaw, Poland.ORCID 0000-0002-2830-5100
Medical University of Warsaw · PLOncoArendi Therapeutics (Poland) · PLInstytut Biologii Doświadczalnej im. Marcelego Nenckiego · PLUniversity College London · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immunotherapy has demonstrated significant activity in a broad range of cancer types, but still the majority of patients receiving it do not maintain durable therapeutic responses. Amino acid metabolism has been proposed to be involved in the regulation of immune response. Here, we investigated in detail the role of arginase 1 (Arg1) in the modulation of antitumor immune response against poorly immunogenic Lewis lung carcinoma. We observed that tumor progression is associated with an incremental increase in the number of Arg1

Indexed as

Carcinoma, Lewis LungLung NeoplasmsAnimalsArginaseHumansLungT-LymphocytesTumor MicroenvironmentArginaseArginasearginase inhibitorimmunosuppressionimmunotherapymyeloid cellst-cells responsetumor microenvironment

Identifiers

PMID34367736
PMCPMC8312619
OpenAlexW3186885003

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.