Evidence map›Paper›PMID 37214210›Full record

ArticleJournal of immunotherapy and precision oncology2023

Translational Studies Using the MALT1 Inhibitor (

Mauro Di Pilato, Yun Gao, Yi Sun, Amina Fu, Carina Grass, Thomas Seeholzer, Regina Feederle, Irina Mazo, Samuel W Kazer, Kevin Litchfield and 5 more

Open access · goldAbstract read
In one paragraph

Article in Journal of immunotherapy and precision oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

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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

15 authors at 4 institutions in 3 countries.

Mauro Di PilatoMD Anderson Cancer Center, University of Texas, Houston, TX, USA.ORCID https://orcid.org/0000-0003-3902-7406
Yun GaoMonopteros Therapeutics, Boston, MA, USA.
Yi SunMassachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA, USA.
Amina FuMassachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA, USA.
Carina GrassResearch Unit Signaling and Translation - Signaling and Immunity, Molecular Targets and Therapeutics Center, Helmholtz Munich-German Research Center for Environmental Health, Neuherberg, Germany.
Thomas SeeholzerResearch Unit Signaling and Translation - Signaling and Immunity, Molecular Targets and Therapeutics Center, Helmholtz Munich-German Research Center for Environmental Health, Neuherberg, Germany.
Regina FeederleMonoclonal Antibody Core Facility, Institute for Diabetes and Obesity, Helmholtz Zentrum München-German Research Center for Environmental Health, Neuherberg, Germany.
Irina MazoMonopteros Therapeutics, Boston, MA, USA.
Samuel W KazerMonopteros Therapeutics, Boston, MA, USA.
Kevin LitchfieldCancer Research UK Lung Cancer Centre of Excellence, University College London Cancer Institute, London, UK.
Ulrich H von AndrianHarvard Medical School, Boston, MA, USA.
Thorsten R MempelHarvard Medical School, Boston, MA, USA.
Russell W JenkinsMassachusetts General Hospital Cancer Center, Harvard Medical School, Boston, MA, USA.
Daniel KrappmannResearch Unit Signaling and Translation - Signaling and Immunity, Molecular Targets and Therapeutics Center, Helmholtz Munich-German Research Center for Environmental Health, Neuherberg, Germany.
Peter KellerMonopteros Therapeutics, Boston, MA, USA.
Harvard University · USHelmholtz Zentrum München · DECancer Research UK · GBThe University of Texas MD Anderson Cancer Center · US

Funding

Strategies to Overcome Immune Resistance in Head and Neck CancersP01CA240239 · NCI · YALE UNIVERSITY · PI SARTOR, MAUREEN AGNES · 2019 to 2023
$8.4M
Cellular mechanisms by which exhausted T cell responses are restoredR01AI123349 · NIAID · MASSACHUSETTS GENERAL HOSPITAL · PI Thorsten Roman Mempel · 2017 to 2026
$4.5M
NCI NIH HHS P01 CA240239NIAID NIH HHS R01 AI123349
6 · The paper itself

Abstract

Introduction: Regulatory T cells (Tregs) play a critical role in the maintenance of immune homeostasis but also protect tumors from immune-mediated growth control or rejection and pose a significant barrier to effective immunotherapy. Inhibition of MALT1 paracaspase activity can selectively reprogram immune-suppressive Tregs in the tumor microenvironment to adopt a proinflammatory fragile state, which offers an opportunity to impede tumor growth and enhance the efficacy of immune checkpoint therapy (ICT). Methods: We performed preclinical studies with the orally available allosteric MALT1 inhibitor ( Results: ( Conclusions: The MALT1 inhibitor (

Indexed as

cancer immunotherapyfragile Tregsinterferon-γMALT1regulatory T cells

Identifiers

PMID37214210
PMCPMC10195017
OpenAlexW4323031655

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.