Evidence map›Paper›PMID 38239354›Full record

ArticleFrontiers in immunology2023

Impaired activation of plasmacytoid dendritic cells

Matilde Monti, Giorgia Ferrari, Valentina Grosso, Francesco Missale, Mattia Bugatti, Valeria Cancila, Stefania Zini, Agnese Segala, Luca La Via, Francesca Consoli and 5 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.2field-weighted citation impact, top 13% 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

11 citing papers in PubMed, 9 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 6 institutions in 3 countries.

Matilde MontiDepartment of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Giorgia FerrariDepartment of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Valentina GrossoDepartment of Biotechnology, University of Verona, Verona, Italy.
Francesco MissaleDepartment of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Mattia BugattiDepartment of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Valeria CancilaTumor Immunology Unit, Department of Health Sciences, University of Palermo, Palermo, Italy.
Stefania ZiniDepartment of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Agnese SegalaDepartment of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Luca La ViaDepartment of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Francesca ConsoliOncology Unit, Azienda Socio Sanitaria Territoriale (ASST) Spedali Civili di Brescia, Brescia, Italy.
Matteo OrlandiDepartment of Biotechnology, University of Verona, Verona, Italy.
Alessandra ValerioDepartment of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
Claudio TripodoTumor Immunology Unit, Department of Health Sciences, University of Palermo, Palermo, Italy.
Marzia RossatoDepartment of Biotechnology, University of Verona, Verona, Italy.
William VermiDepartment of Molecular and Translational Medicine, University of Brescia, Brescia, Italy.
University of Brescia · ITUniversity of Verona · ITUniversity of Palermo · ITAzienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia · ITThe Netherlands Cancer Institute · NLWashington University in St. Louis · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Plasmacytoid dendritic cells (pDCs) infiltrate a large set of human cancers. Interferon alpha (IFN-α) produced by pDCs induces growth arrest and apoptosis in tumor cells and modulates innate and adaptive immune cells involved in anti-cancer immunity. Moreover, effector molecules exert tumor cell killing. However, the activation state and clinical relevance of pDCs infiltration in cancer is still largely controversial. In Primary Cutaneous Melanoma (PCM), pDCs density decreases over disease progression and collapses in metastatic melanoma (MM). Moreover, the residual circulating pDC compartment is defective in IFN-α production. Methods: The activation of tumor-associated pDCs was evaluated by Results: Based on a set of microscopic, functional and Discussion: These findings propose a new window of intervention for novel immunotherapy approaches to amplify the antitumor innate immune response in cutaneous melanoma (CM).

Indexed as

MelanomaSkin NeoplasmsCytokinesDendritic CellsHumansImmunosuppressive AgentsInterferon-alphaNucleotidyltransferasesToll-Like Receptor 7Toll-Like Receptor 9CytokinesImmunosuppressive AgentsInterferon-alphaNucleotidyltransferasesToll-Like Receptor 7Toll-Like Receptor 9cGAS-STINGglycolysisinterferonmelanomaplasmacytoid dendritic cellsTGF-βtoll-like receptortumor microenvironment

Identifiers

PMID38239354
PMCPMC10795195
OpenAlexW4390542376

What OpenQuestion holds

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LicenceCC BY
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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.