Evidence map›Paper›PMID 34277006›Full record

ArticleClinical & translational immunology2021

Type 1 conventional dendritic cells and interferons are required for spontaneous CD4

Raphaël Mattiuz, Carine Brousse, Marc Ambrosini, Jean-Charles Cancel, Gilles Bessou, Julie Mussard, Amélien Sanlaville, Christophe Caux, Nathalie Bendriss-Vermare, Jenny Valladeau-Guilemond and 2 more

Open access · goldAbstract read
In one paragraph

Article in Clinical & translational immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
3.4field-weighted citation impact, top 6% 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

27 citing papers in PubMed, 54 citations in OpenAlex.

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  5. Dendritic cell maturation in cancer.Nature reviews. Cancer · 2025
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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

12 authors at 2 institutions in 2 countries.

Raphaël MattiuzCentre d'Immunologie de Marseille-Luminy Turing Center for Living Systems CNRS INSERM Aix Marseille Univ Marseille France.ORCID https://orcid.org/0000-0002-3292-1635
Carine BrousseCentre d'Immunologie de Marseille-Luminy Turing Center for Living Systems CNRS INSERM Aix Marseille Univ Marseille France.
Marc AmbrosiniCentre d'Immunologie de Marseille-Luminy Turing Center for Living Systems CNRS INSERM Aix Marseille Univ Marseille France.
Jean-Charles CancelCentre d'Immunologie de Marseille-Luminy Turing Center for Living Systems CNRS INSERM Aix Marseille Univ Marseille France.
Gilles BessouCentre d'Immunologie de Marseille-Luminy Turing Center for Living Systems CNRS INSERM Aix Marseille Univ Marseille France.
Julie MussardINSERM 1052 CNRS 5286 Centre Léon Bérard Cancer Research Center of Lyon Univ Lyon Université Claude Bernard Lyon 1 Lyon France.
Amélien SanlavilleINSERM 1052 CNRS 5286 Centre Léon Bérard Cancer Research Center of Lyon Univ Lyon Université Claude Bernard Lyon 1 Lyon France.
Christophe CauxINSERM 1052 CNRS 5286 Centre Léon Bérard Cancer Research Center of Lyon Univ Lyon Université Claude Bernard Lyon 1 Lyon France.
Nathalie Bendriss-VermareINSERM 1052 CNRS 5286 Centre Léon Bérard Cancer Research Center of Lyon Univ Lyon Université Claude Bernard Lyon 1 Lyon France.ORCID https://orcid.org/0000-0002-8771-3585
Jenny Valladeau-GuilemondINSERM 1052 CNRS 5286 Centre Léon Bérard Cancer Research Center of Lyon Univ Lyon Université Claude Bernard Lyon 1 Lyon France.
Marc DalodCentre d'Immunologie de Marseille-Luminy Turing Center for Living Systems CNRS INSERM Aix Marseille Univ Marseille France.ORCID https://orcid.org/0000-0002-6436-7966
Karine CrozatCentre d'Immunologie de Marseille-Luminy Turing Center for Living Systems CNRS INSERM Aix Marseille Univ Marseille France.ORCID https://orcid.org/0000-0003-4761-3675
Centre National de la Recherche Scientifique · FRUniversité Claude Bernard Lyon 1 · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesTo better understand how immune responses may be harnessed against breast cancer, we investigated which immune cell types and signalling pathways are required for spontaneous control of a mouse model of mammary adenocarcinoma.

methodsThe NOP23 mammary adenocarcinoma cell line expressing epitopes derived from the ovalbumin model antigen is spontaneously controlled when orthotopically engrafted in syngeneic C57BL/6 mice. We combined this breast cancer model with antibody-mediated depletion of lymphocytes and with mutant mice affected in interferon (IFN) or type 1 conventional dendritic cell (cDC1) responses. We monitored tumor growth and immune infiltration including the activation of cognate ovalbumin-specific T cells.

resultsBreast cancer immunosurveillance required cDC1, NK/NK T cells, conventional CD4

conclusionInterferons and cDC1 are critical for breast cancer immunosurveillance. IFN-γ plays a prominent role over IFN-I in licensing cDC1 for efficient T-cell activation.

Indexed as

breast cancercancer immunosurveillanceCD4+ T cellsCD8+ T cellscDC1IFN‐γinterferons

Identifiers

PMID34277006
PMCPMC8279130
OpenAlexW3185336537

What OpenQuestion 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 OpenQuestion graph.