Evidence map›Paper›PMID 34467246›Full record

ArticleCell reports. Medicine2021

Soluble trivalent engagers redirect cytolytic T cell activity toward tumor endothelial marker 1.

Julie K Fierle, Matteo Brioschi, Mariastella de Tiani, Laureline Wetterwald, Vasileios Atsaves, Johan Abram-Saliba, Tatiana V Petrova, George Coukos, Steven M Dunn

Open access · goldAbstract read
In one paragraph

Article in Cell reports. Medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.0field-weighted citation impact, top 21% 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

12 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Review
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  4. Inflammatory CD248Nature cardiovascular research · 2025
    Article
  5. Article
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  7. Article
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  10. Application Progress of the Single Domain Antibody in Medicine.International journal of molecular sciences · 2023
    Review
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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

9 authors at 2 institutions in 1 country.

Julie K FierleLAbCore Immunoglobulin Discovery Platform, Department of Oncology, Ludwig Institute for Cancer Research Lausanne, University of Lausanne, 1066 Epalinges, Switzerland.
Matteo BrioschiLAbCore Immunoglobulin Discovery Platform, Department of Oncology, Ludwig Institute for Cancer Research Lausanne, University of Lausanne, 1066 Epalinges, Switzerland.
Mariastella de TianiLAbCore Immunoglobulin Discovery Platform, Department of Oncology, Ludwig Institute for Cancer Research Lausanne, University of Lausanne, 1066 Epalinges, Switzerland.
Laureline WetterwaldDepartment of Oncology, Ludwig Institute for Cancer Research Lausanne, University of Lausanne, 1066 Epalinges, Switzerland.
Vasileios AtsavesLAbCore Immunoglobulin Discovery Platform, Department of Oncology, Ludwig Institute for Cancer Research Lausanne, University of Lausanne, 1066 Epalinges, Switzerland.
Johan Abram-SalibaLAbCore Immunoglobulin Discovery Platform, Department of Oncology, Ludwig Institute for Cancer Research Lausanne, University of Lausanne, 1066 Epalinges, Switzerland.
Tatiana V PetrovaDepartment of Oncology, Ludwig Institute for Cancer Research Lausanne, University of Lausanne, 1066 Epalinges, Switzerland.
George CoukosDepartment of Oncology, Ludwig Institute for Cancer Research Lausanne, Lausanne University Hospital and University of Lausanne, 1005 Lausanne, Switzerland.
Steven M DunnLAbCore Immunoglobulin Discovery Platform, Department of Oncology, Ludwig Institute for Cancer Research Lausanne, University of Lausanne, 1066 Epalinges, Switzerland.
Ludwig Cancer Research · CHUniversity of Lausanne · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor endothelial marker 1 (TEM1) is an emerging cancer target with a unique dual expression profile. First, TEM1 is expressed in the stroma and neo-vasculature of many human carcinomas but is largely absent from healthy adult tissues. Second, TEM1 is expressed by tumor cells of mesenchymal origin, notably sarcoma. Here, we present two fully human anti-TEM1 single-chain variable fragment (scFv) reagents, namely, 1C1m and 7G22, that recognize distinct regions of the extracellular domain and possess substantially different affinities. In contrast to other, well-described anti-TEM1 binders, these fragments confer cytolytic activity when expressed as 2

Indexed as

AnimalsAntigens, CDAntigens, NeoplasmCell Line, TumorClone CellsFemaleHumansMiceProtein BindingProtein MultimerizationReceptors, Chimeric AntigenSingle-Chain AntibodiesSolubilityT-Lymphocytes, CytotoxicXenograft Model Antitumor AssaysAntigens, CDAntigens, NeoplasmCD248 protein, humanReceptors, Chimeric AntigenSingle-Chain AntibodiesBiTEcancer immunotherapyCARendosialin/CD248sarcomaT cell engagerTEM1

Identifiers

PMID34467246
PMCPMC8385295
OpenAlexW3188598573

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.