Evidence map›Paper›PMID 34282787›Full record

ArticleCancers2021

Alpha-Fetoprotein- and CD40Ligand-Expressing Dendritic Cells for Immunotherapy of Hepatocellular Carcinoma.

Annabelle Vogt, Farsaneh Sadeghlar, Tiyasha H Ayub, Carlo Schneider, Christian Möhring, Taotao Zhou, Robert Mahn, Alexandra Bartels, Michael Praktiknjo, Miroslaw T Kornek and 7 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

17 citing papers in PubMed, 21 citations in OpenAlex.

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  15. [Can tumor vaccines really cure liver cancer?]Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology · 2022
    Article
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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

17 authors at 2 institutions in 1 country.

Annabelle VogtDepartment of Internal Medicine I, University Hospital of Bonn, 53127 Bonn, Germany.
Farsaneh SadeghlarDepartment of Internal Medicine I, University Hospital of Bonn, 53127 Bonn, Germany.
Tiyasha H AyubDepartment of Internal Medicine I, University Hospital of Bonn, 53127 Bonn, Germany.
Carlo SchneiderDepartment of Internal Medicine I, University Hospital of Bonn, 53127 Bonn, Germany.
Christian MöhringDepartment of Internal Medicine I, University Hospital of Bonn, 53127 Bonn, Germany.ORCID 0000-0001-7651-4401
Taotao ZhouDepartment of Internal Medicine I, University Hospital of Bonn, 53127 Bonn, Germany.
Robert MahnDepartment of Internal Medicine I, University Hospital of Bonn, 53127 Bonn, Germany.ORCID 0000-0001-8312-6511
Alexandra BartelsDepartment of Internal Medicine I, University Hospital of Bonn, 53127 Bonn, Germany.
Michael PraktiknjoDepartment of Internal Medicine I, University Hospital of Bonn, 53127 Bonn, Germany.ORCID 0000-0001-7033-9956
Miroslaw T KornekDepartment of Internal Medicine I, University Hospital of Bonn, 53127 Bonn, Germany.ORCID 0000-0002-1682-1765
Marieta TomaDepartment of Pathology, University Hospital of Bonn, 53127 Bonn, Germany.
Ingo G H Schmidt-WolfDepartment of Integrated Oncology (CIO), University of Bonn, 53127 Bonn, Germany.
Vittorio BranchiDepartment of Visceral Surgery, University Hospital of Bonn, 53127 Bonn, Germany.ORCID 0000-0002-6182-835X
Hanno MatthaeiDepartment of Visceral Surgery, University Hospital of Bonn, 53127 Bonn, Germany.
Jörg C KalffDepartment of Visceral Surgery, University Hospital of Bonn, 53127 Bonn, Germany.
Christian P StrassburgDepartment of Internal Medicine I, University Hospital of Bonn, 53127 Bonn, Germany.
Maria A Gonzalez-CarmonaDepartment of Internal Medicine I, University Hospital of Bonn, 53127 Bonn, Germany.ORCID 0000-0003-3956-1457
University Hospital Bonn · DEUniversity of Bonn · DE

Funding

Deutsche Forschungsgemeinschaft GO 1847/1-2Deutsche Krebshilfe 109255University Hospital of Bonn BONFOR
6 · The paper itself

Abstract

Dendritic cells (DC) as professional antigen presenting cells are able to prime T-cells against the tumor-associated antigen α-fetoprotein (AFP) for immunotherapy of hepatocellular carcinoma (HCC). However, a strong immunosuppressive tumor environment limits their efficacy in patients. The co-stimulation with CD40Ligand (CD40L) is critical in the maturation of DC and T-cell priming. In this study, the impact of intratumoral (i.t.) CD40L-expressing DC to improve vaccination with murine (m)AFP-transduced DC (Ad-mAFP-DC) was analyzed in subcutaneous (s.c.) and orthotopic murine HCC. Murine DC were adenovirally transduced with Ad-mAFP or Ad-CD40L. Hepa129-mAFP-cells were injected into the right flank or the liver of C3H-mice to induce subcutaneous (s.c.) and orthotopic HCC. For treatments, 10

Indexed as

alpha-fetoproteinCD40Liganddendritic cellshepatocellular carcinomasubcutaneous and orthotopic murine HCC

Identifiers

PMID34282787
PMCPMC8269346
OpenAlexW3179233595

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.