Evidence map›Paper›PMID 41116979›Full record

ArticleHLA2025

LMP2A-Targeting CAR-T Cells Equipped With Inducible IL-18 to Address EBV-Associated Malignancies.

Anna Christina Dragon, Stefanie Thoelke, Philip Mausberg, Katharina Zimmermann, Rainer Blasczyk, Michael Hudecek, Hinrich Abken, Axel Schambach, Britta Maecker-Kolhoff, Britta Eiz-Vesper

Abstract read
In one paragraph

Article in HLA, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–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

2 citing papers in PubMed.

  1. Review
  2. Article
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.

Anna Christina DragonHannover Medical School, Institute of Transfusion Medicine and Transplant Engineering, Hannover, Germany.ORCID 0000-0002-5228-7627
Stefanie ThoelkeHannover Medical School, Institute of Transfusion Medicine and Transplant Engineering, Hannover, Germany.
Philip MausbergHannover Medical School, Institute of Transfusion Medicine and Transplant Engineering, Hannover, Germany.
Katharina ZimmermannInstitute of Experimental Hematology, Hannover Medical School, Hannover, Germany.
Rainer BlasczykHannover Medical School, Institute of Transfusion Medicine and Transplant Engineering, Hannover, Germany.
Michael HudecekCellular Immunotherapy, Department of Internal Medicine II, University of Wuerzburg, Wuerzburg, Germany.
Hinrich AbkenDepartment Genetic Immunotherapy, Leibniz Institute for Immunotherapy, Regensburg, Germany.
Axel SchambachInstitute of Experimental Hematology, Hannover Medical School, Hannover, Germany.
Britta Maecker-KolhoffDepartment of Pediatric Hematology and Oncology, Hannover Medical School, Hannover, Germany.
Britta Eiz-VesperHannover Medical School, Institute of Transfusion Medicine and Transplant Engineering, Hannover, Germany.ORCID 0000-0001-8378-3298

Funding

Deutsche Forschungsgemeinschaft SFB900/B11Else Kröner-Fresenius Foundation (EKFS) 2022_EKMK.13German Center for Infection Research (DZIF) TTU07.835Hannover Biomedical Research School (HBRS)Stiftung Deutsche Krebshilfe #111975Stiftung Deutsche Krebshilfe #70115200
6 · The paper itself

Abstract

Epstein-Barr virus (EBV) infects up to 95% of the world's population and persists in B cells and epithelial cells. Uncontrolled proliferation of EBV-infected cells can result in the development of EBV-associated malignancies, for example, post-transplant lymphoproliferative disorder (PTLD) or nasopharyngeal cancer (NPC). It is estimated that 1.8% of deaths due to cancer worldwide are associated with EBV, and the treatment options are limited. As a new therapeutic approach, we developed chimeric antigen receptor T cells targeting EBV-derived latent membrane protein 2A (LMP2A_CAR-Ts). To enable specific elimination of malignant B cells infected with the intracellular pathogen, we utilised T-cell receptor (TCR)-like specificity to generate a CAR against the LMP2A-derived peptide CLGGLLTMV (CLG) presented in the context of HLA-A*02:01. To increase functionality in the tumour microenvironment, LMP2A_CAR-Ts were additionally equipped with inducible release of IL-12 (LMP2A_iIL-12_TRUCKs) or IL-18 (LMP2A_iIL-18_TRUCKs). LMP2A_CAR-Ts and LMP2A_iIL-18_TRUCKs specifically recognised HLA-A*02:01

Indexed as

Epstein-Barr Virus InfectionsHerpesvirus 4, HumanImmunotherapy, AdoptiveInterleukin-18Nasopharyngeal NeoplasmsReceptors, Chimeric AntigenViral Matrix ProteinsB-LymphocytesCell Line, TumorHLA-A2 AntigenHumansTumor MicroenvironmentEBV-associated membrane antigen, Epstein-Barr virusHLA-A2 AntigenInterleukin-18Receptors, Chimeric AntigenViral Matrix ProteinsCAR‐T cellsEBV‐associated malignanciesinducible cytokine expressionLMP2APTLDTCR‐like antibodyTCR‐like CARTRUCKs

Identifiers

PMID41116979
PMCPMC12538270

What OpenQuestion holds

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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.