Evidence map›Paper›PMID 39272178›Full record

ArticleJournal of experimental & clinical cancer research : CR2024

In vivo CAR T cell therapy against angioimmunoblastic T cell lymphoma.

Adrien Krug, Aymen Saidane, Chiara Martinello, Floriane Fusil, Alexander Michels, Christian J Buchholz, Jean-Ehrland Ricci, Els Verhoeyen

Abstract read
In one paragraph

Article in Journal of experimental & clinical cancer research : CR, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

14 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Review
  5. In vivo chimeric antigen receptor (CAR)-T cell therapy.Nature reviews. Drug discovery · 2026
    Review
  6. Article
  7. Review
  8. Oncology research · 2026
    Review
  9. In vivo CAR cell therapy: from bench to bedside.Journal of hematology & oncology · 2025
    Review
  10. Review
  11. Review
  12. Article
  13. Review
  14. 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

8 authors.

Adrien Krug *Université Côte d'Azur, INSERM, C3M, 06204, Nice, France.
Aymen Saidane *Université Côte d'Azur, INSERM, C3M, 06204, Nice, France.
Chiara Martinello *Université Côte d'Azur, INSERM, C3M, 06204, Nice, France.
Floriane FusilCIRI - International Center for Infectiology Research, Inserm, U1111, Université Claude Bernard Lyon 1, CNRS, UMR5308, Ecole Normale Supérieure de Lyon, Université Lyon, F-69007, Lyon, France.
Alexander MichelsMolecular Biotechnology and Gene Therapy, Paul-Ehrlich-Institut, 63225, Langen, Germany.
Christian J BuchholzMolecular Biotechnology and Gene Therapy, Paul-Ehrlich-Institut, 63225, Langen, Germany.
Jean-Ehrland Ricci *Université Côte d'Azur, INSERM, C3M, 06204, Nice, France.
Els Verhoeyen *Université Côte d'Azur, INSERM, C3M, 06204, Nice, France. els.verhoeyen@unice.fr.ORCID http://orcid.org/0000-0001-9224-5491

Funding

Agence Nationale de la Recherche ANR-16-CE16-0024-01H2020 Marie Skłodowska-Curie Actions GET-INMinistère de l'Enseignement Supérieur et de la Recherche PhD followship
6 · The paper itself

Abstract

backgroundFor angioimmunoblastic T cell lymphoma (AITL), a rare cancer, no specific treatments are available and survival outcome is poor. We previously developed a murine model for AITL that mimics closely human disease and allows to evaluate new treatments. As in human AITL, the murine CD4

methodsTo prevent fratricide among CAR T cells when delivering an CD4-specific CAR, we used a lentiviral vector (LV) encoding an anti-CD4 CAR, allowing exclusive entry into CD8 T cells.

resultsThese anti-CD4CAR CD8-targeted LVs achieved in murine AITL biopsies high CAR-expression levels in CD8 T cells. Malignant CD4 Tfh cells were eliminated from the mAITL lymphoma, while the CAR + CD8 T cells expanded upon encounter with the CD4 receptor and were shaped into functional cytotoxic cells. Finally, in vivo injection of the CAR + CD8-LVs into our preclinical AITL mouse model carrying lymphomas, significantly prolonged mice survival. Moreover, the in vivo generated functional CAR + CD8 T cells efficiently reduced neoplastic T cell numbers in the mAITL tumors.

conclusionThis is the first description of in vivo generated CAR T cells for therapy of a T cell lymphoma. The strategy described offers a new therapeutic concept for patients suffering from CD4-driven T cell lymphomas.

Indexed as

Disease Models, AnimalImmunotherapy, AdoptiveLymphoma, T-CellReceptors, Chimeric AntigenAnimalsCD8-Positive T-LymphocytesCell Line, TumorHumansImmunoblastic LymphadenopathyMiceReceptors, Chimeric AntigenAITLCancer therapyCAR TCD8-targeted virus envelopeIn vivo gene therapyLentiviral vectorPreclinical modelPseudotypingT cell lymphoma

Identifiers

PMID39272178
PMCPMC11401350

What Socratic 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 Socratic graph.