Evidence map›Paper›PMID 42104273›Full record

ArticleBMC cancer2026

A novel Chimeric Antigen Receptor (CAR) - strategy to target EGFR

Kristi Vera, Gülen Esken, Jin Wook Hwang, Carine Elbaz, Diana Chaker, Noufissa Oudrhiri, Christophe Desterke, Frank Griscelli, Annelise Bennaceur-Griscelli, Ali G Turhan

Abstract read
In one paragraph

Article in BMC cancer, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Kristi VeraINSERM UMR-S-1310, Paris Saclay University, Villejuif, 94800, France.
Gülen EskenINSERM UMR-S-1310, Paris Saclay University, Villejuif, 94800, France.
Jin Wook HwangINSERM UMR-S-1310, Paris Saclay University, Villejuif, 94800, France.
Carine ElbazINSERM UMR-S-1310, Paris Saclay University, Villejuif, 94800, France.
Diana ChakerINSERM UMR-S-1310, Paris Saclay University, Villejuif, 94800, France.
Noufissa OudrhiriINSERM UMR-S-1310, Paris Saclay University, Villejuif, 94800, France.
Christophe DesterkeINSERM UMR-S-1310, Paris Saclay University, Villejuif, 94800, France.
Frank GriscelliINSERM UMR-S-1310, Paris Saclay University, Villejuif, 94800, France.
Annelise Bennaceur-GriscelliINSERM UMR-S-1310, Paris Saclay University, Villejuif, 94800, France.
Ali G TurhanINSERM UMR-S-1310, Paris Saclay University, Villejuif, 94800, France. turviv33@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAutologous chimeric antigen receptor (CAR) expressing T-Cells (CAR-T) have been efficiently used in hematological malignancies but their efficacy in solid tumors remains limited. CAR therapies via the use of macrophages, offer a promising avenue due to their unique ability to infiltrate tumors and to initiate phagocytosis.

methodsTo generate a preclinical model of CAR-Macs, we have designed a novel CAR-construct to target EGFR

resultsTHP-1 cell line expressing CAR and control constructs were generated via lentiviral transduction followed by generation of monocytes and CAR-expressing M1 macrophages (CAR-Macs). To evaluate their ability of phagocytosis, we co-cultured THP-1 derived WT macrophages or CAR-Macs in the presence of target DK-MG cells. Confocal microscopy experiments revealed highly efficient phagocytosis of DK-MG EGFR

conclusionsThe model described in this work is suitable for allowing translation to iPSC-derived macrophages to generate clinically applicable future cell therapy approaches in solid tumors expressing mutated variant EGFR

Indexed as

Brain NeoplasmsErbB ReceptorsGlioblastomaImmunotherapy, AdoptiveMacrophagesReceptors, Chimeric AntigenCell Line, TumorHumansMutationPhagocytosisTHP-1 Cellsepidermal growth factor receptor VIIIErbB ReceptorsReceptors, Chimeric AntigenEGFRvIIIGlioblastomaMacrophages: CAR-MacrophagesPhagocytosis

Identifiers

PMID42104273
PMCPMC13321683

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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.