Evidence map›Paper›PMID 31234464›Full record

ArticleCancers2019

Evaluating a Single Domain Antibody Targeting Human PD-L1 as a Nuclear Imaging and Therapeutic Agent.

Katrijn Broos, Quentin Lecocq, Catarina Xavier, Jessica Bridoux, Tham T Nguyen, Jurgen Corthals, Steve Schoonooghe, Eva Lion, Geert Raes, Marleen Keyaerts and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cancers, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
3.6field-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

44 citing papers in PubMed, 68 citations in OpenAlex.

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  11. Cell Model for Testing Pharmaceuticals Targeting Human PD-L1.Sovremennye tekhnologii v meditsine · 2024
    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

12 authors at 2 institutions in 1 country.

Katrijn BroosLaboratory for Molecular and Cellular therapy (LMCT), Vrije Universiteit Brussel, Laarbeeklaan 103, B-1090 Brussels, Belgium. katrijn.broos@vub.ac.be.
Quentin LecocqLaboratory for Molecular and Cellular therapy (LMCT), Vrije Universiteit Brussel, Laarbeeklaan 103, B-1090 Brussels, Belgium. quentin.lecocq@vub.be.
Catarina XavierIn Vivo Cellular and Molecular Imaging Laboratory (ICMI), Vrije Universiteit Brussel, Laarbeeklaan 103, B-1090 Brussels, Belgium. catarina.xavier@vub.be.
Jessica BridouxIn Vivo Cellular and Molecular Imaging Laboratory (ICMI), Vrije Universiteit Brussel, Laarbeeklaan 103, B-1090 Brussels, Belgium. Jessica.Bridoux@vub.be.
Tham T NguyenIn Vivo Cellular and Molecular Imaging Laboratory (ICMI), Vrije Universiteit Brussel, Laarbeeklaan 103, B-1090 Brussels, Belgium. thamnt.vn@gmail.com.
Jurgen CorthalsLaboratory for Molecular and Cellular therapy (LMCT), Vrije Universiteit Brussel, Laarbeeklaan 103, B-1090 Brussels, Belgium. jurgen.corthals@vub.be.
Steve SchoonoogheLaboratory of Cellular and Molecular Immunology (CMIM), Vrije Universiteit Brussel, Pleinlaan 2, B-1050 Brussels, Belgium. steve.schoonooghe@vub.vib.be.
Eva LionLaboratory of Experimental Hematology, Vaccine and Infectious Disease Institute (VAXINFECTIO), Faculty of Medicine and Health Sciences, University of Antwerp, Universiteitsplein 1, B-2610 Antwerp, Belgium. eva.lion@uantwerpen.be.
Geert RaesLaboratory of Cellular and Molecular Immunology (CMIM), Vrije Universiteit Brussel, Pleinlaan 2, B-1050 Brussels, Belgium. geert.raes@vub.be.
Marleen KeyaertsIn Vivo Cellular and Molecular Imaging Laboratory (ICMI), Vrije Universiteit Brussel, Laarbeeklaan 103, B-1090 Brussels, Belgium. marleen.keyaerts@uzbrussel.be.
Nick DevoogdtIn Vivo Cellular and Molecular Imaging Laboratory (ICMI), Vrije Universiteit Brussel, Laarbeeklaan 103, B-1090 Brussels, Belgium. ndevoogd@vub.be.
Karine BreckpotLaboratory for Molecular and Cellular therapy (LMCT), Vrije Universiteit Brussel, Laarbeeklaan 103, B-1090 Brussels, Belgium. karine.breckpot@vub.be.
Vrije Universiteit Brussel · BEUniversity of Antwerp · BE

Funding

Agency of Innovation by Science and Technology IWT711Fonds Wetenschappelijk Onderzoek FWOSB43H2020 Marie Skłodowska-Curie Actions H2020-MSCA-ITN PET3DKom op tegen Kanker ANI144Kom op tegen Kanker ANI173Kom op tegen Kanker ANI209Melanoma Research Alliance 509516Stichting Tegen Kanker ANI184
6 · The paper itself

Abstract

The PD-1:PD-L1 immune checkpoint axis is central in the escape of cancer cells from anticancer immune responses. Monoclonal antibodies (mAbs) specific for PD-L1 have been approved for treatment of various cancer types. Although PD-L1 blockade has proven its merit, there are still several aspects that require further attention to fully capitalize on its potential. One of these is the development of antigen-binding moieties that enable PD-L1 diagnosis and therapy. We generated human PD-L1 binding single domain antibodies (sdAbs) and selected sdAb K2, a sdAb with a high affinity for PD-L1, as a lead compound. SPECT/CT imaging in mice following intravenous injection of Technetium-99m (

Indexed as

avelumabcancerimmune checkpointimmunotherapymonoclonal antibodynanobodyPD-1PD-L1single domain antibodyT cell

Identifiers

PMID31234464
PMCPMC6628009
OpenAlexW2950319031

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.