Evidence map›Paper›PMID 33488625›Full record

ArticleFrontiers in immunology2020

Case Report: An EGFR-Targeted 4-1BB-agonistic Trimerbody Does Not Induce Hepatotoxicity in Transgenic Mice With Liver Expression of Human EGFR.

Marta Compte, Seandean L Harwood, Jorge Martínez-Torrecuadrada, Gema Perez-Chacon, Patricia González-García, Antonio Tapia-Galisteo, Paul M P Van Bergen En Henegouwen, Aránzazu Sánchez, Isabel Fabregat, Laura Sanz and 2 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Targeting Co-Stimulatory Receptors of the TNF Superfamily for Cancer Immunotherapy.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2023
    Review
  3. Article
  4. Review
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 9 institutions in 3 countries.

Marta CompteDepartment of Antibody Engineering, Leadartis SL, Madrid, Spain.
Seandean L HarwoodDepartment of Molecular Biology, Aarhus University, Aarhus, Denmark.
Jorge Martínez-TorrecuadradaSpanish National Cancer Research Center (CNIO), Madrid, Spain.
Gema Perez-ChaconInstituto de Investigaciones Biomédicas Alberto Sols (IIBm), CSIC-UAM, Madrid, Spain.
Patricia González-GarcíaSpanish National Cancer Research Center (CNIO), Madrid, Spain.
Antonio Tapia-GalisteoMolecular Immunology Unit, Hospital Universitario Puerta de Hierro Majadahonda, Madrid, Spain.
Paul M P Van Bergen En HenegouwenDivision of Cell Biology, Department of Biology, Science Faculty, Utrecht University, Utrecht, Netherlands.
Aránzazu SánchezDepartment of Biochemistry and Molecular Biology, Faculty of Pharmacy, Complutense University of Madrid (UCM), Health Research Institute of the Hospital Clínico San Carlos (IdISSC), Madrid, Spain.
Isabel FabregatOncobell Program, Bellvitge Biomedical Research Institute (IDIBELL), CIBEREHD and University of Barcelona, L'Hospitalet de Llobregat, Barcelona, Spain.
Laura SanzMolecular Immunology Unit, Hospital Universitario Puerta de Hierro Majadahonda, Madrid, Spain.
Juan M ZapataInstituto de Investigaciones Biomédicas Alberto Sols (IIBm), CSIC-UAM, Madrid, Spain.
Luis Alvarez-VallinaCancer Immunotherapy Unit (UNICA), Department of Immunology, Hospital Universitario 12 de Octubre, Madrid, Spain.
Hospital La Paz Institute for Health Research · ESHospital Universitario Puerta de Hierro Majadahonda · ESAarhus University · DKCentro de Investigación Biomédica en Red · ESCentro de Investigación del Cáncer · ESResearch Institute Hospital 12 de Octubre · ESSpanish National Cancer Research Centre · ESUniversidad Complutense de Madrid · ESUtrecht University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Agonistic monoclonal antibodies (mAbs) targeting the co-stimulatory receptor 4-1BB are among the most effective immunotherapeutic agents across pre-clinical cancer models. However, clinical development of full-length 4-1BB agonistic mAbs, has been hampered by dose-limiting liver toxicity. We have previously developed an EGFR-targeted 4-1BB-agonistic trimerbody (1D8

Indexed as

4-1BB LigandAnimalsAntibodies, MonoclonalAntineoplastic Agents, ImmunologicalChemical and Drug Induced Liver InjuryColorectal NeoplasmsDrug-Related Side Effects and Adverse ReactionsErbB ReceptorsFemaleHEK293 CellsHepatocytesHumansImmunotherapyMiceMice, Inbred C57BLMice, Transgenic4-1BB LigandAntibodies, MonoclonalAntineoplastic Agents, ImmunologicalEGFR protein, humanErbB Receptors4-1BB agonistscancer immunotherapyEGFREGFR-targeted 4-1BB agonistshepatotoxicityimmunostimulatory antibodiestrimerbodies

Identifiers

PMID33488625
PMCPMC7817978
OpenAlexW3121049959

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.