Evidence map›Paper›PMID 38031106›Full record

ArticleMolecular cancer2023

A bispecific Clec9A-PD-L1 targeted type I interferon profoundly reshapes the tumor microenvironment towards an antitumor state.

Sandra Van Lint, Alexander Van Parys, Bram Van Den Eeckhout, Niels Vandamme, Stephane Plaisance, Annick Verhee, Dominiek Catteeuw, Elke Rogge, Jennifer De Geest, Nele Vanderroost and 6 more

Open access · goldAbstract read
In one paragraph

Article in Molecular cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 20% 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, 1 synthesis or guideline pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
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

16 authors at 4 institutions in 3 countries.

Sandra Van LintCenter for Medical Biotechnology, VIB & Department of Biomolecular Medicine, Ghent University, Ghent, Belgium.
Alexander Van ParysCenter for Medical Biotechnology, VIB & Department of Biomolecular Medicine, Ghent University, Ghent, Belgium.
Bram Van Den EeckhoutCenter for Medical Biotechnology, VIB & Department of Biomolecular Medicine, Ghent University, Ghent, Belgium.
Niels VandammeCancer Research Institute Ghent (CRIG), Ghent, Belgium.
Stephane PlaisanceVIB Nucleomics Core, Leuven, Belgium.
Annick VerheeCenter for Medical Biotechnology, VIB & Department of Biomolecular Medicine, Ghent University, Ghent, Belgium.
Dominiek CatteeuwCenter for Medical Biotechnology, VIB & Department of Biomolecular Medicine, Ghent University, Ghent, Belgium.
Elke RoggeCenter for Medical Biotechnology, VIB & Department of Biomolecular Medicine, Ghent University, Ghent, Belgium.
Jennifer De GeestCenter for Medical Biotechnology, VIB & Department of Biomolecular Medicine, Ghent University, Ghent, Belgium.
Nele VanderroostCenter for Medical Biotechnology, VIB & Department of Biomolecular Medicine, Ghent University, Ghent, Belgium.
Jana RoelsVIB Single Cell Core, VIB, Ghent-Leuven, Belgium.
Yvan SaeysData Mining and Modelling for Biomedicine, VIB & Center for inflammation research, Ghent University, Ghent, Belgium.
Gilles UzéIRMB, University Montpellier, INSERM, CNRS, Montpellier, France.
Niko KleyOrionis Biosciences, Ghent, Belgium.
Anje CauwelsCenter for Medical Biotechnology, VIB & Department of Biomolecular Medicine, Ghent University, Ghent, Belgium.
Jan TavernierCenter for Medical Biotechnology, VIB & Department of Biomolecular Medicine, Ghent University, Ghent, Belgium. jan.tavernier@vib-ugent.be.
Ghent University · BEVIB-UGent Center for Medical Biotechnology · BECentre National de la Recherche Scientifique · FROrion Corporation (United Kingdom) · GB

Funding

European Research Council CYRE, 340941
6 · The paper itself

Abstract

Despite major improvements in immunotherapeutic strategies, the immunosuppressive tumor microenvironment remains a major obstacle for the induction of efficient antitumor responses. In this study, we show that local delivery of a bispecific Clec9A-PD-L1 targeted type I interferon (AcTaferon, AFN) overcomes this hurdle by reshaping the tumor immune landscape.Treatment with the bispecific AFN resulted in the presence of pro-immunogenic tumor-associated macrophages and neutrophils, increased motility and maturation profile of cDC1 and presence of inflammatory cDC2. Moreover, we report empowered diversity in the CD8

Indexed as

Interferon Type INeoplasmsB7-H1 AntigenCD8-Positive T-LymphocytesCell Line, TumorHumansImmunotherapyTumor MicroenvironmentB7-H1 AntigenInterferon Type IAcTakineCancer immunotherapyImmune checkpointTumor microenvironmentType I Interferon

Identifiers

PMID38031106
PMCPMC10685570
OpenAlexW4389141675

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.