Evidence map›Paper›PMID 42148107›Full record

ArticleFrontiers in immunology2026

Blocking CD30 on CD19 CAR T cells augments their functional capacities against B-cell leukemia/lymphoma.

Tim Schlierkamp-Voosen, Markus Barden, Helena Janning, Marcell Kaljanac, Dennis Christoph Harrer, Celine Dreger, Kathrin Hammon, Moritz Ertelt, Clara T Schoeder, Hólmfridur Rósa Halldórsdóttir and 4 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 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
0cells of the map it votes in
0citing 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

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

14 authors.

Tim Schlierkamp-VoosenDiv. Genetic Immunotherapy, Leibniz Institute for Immunotherapy, Regensburg, Germany.
Markus BardenDiv. Genetic Immunotherapy, Leibniz Institute for Immunotherapy, Regensburg, Germany.
Helena JanningDepartment of Internal Medicine III, University Hospital Regensburg, Regensburg, Germany.
Marcell KaljanacDiv. Genetic Immunotherapy, Leibniz Institute for Immunotherapy, Regensburg, Germany.
Dennis Christoph HarrerDepartment of Internal Medicine III, University Hospital Regensburg, Regensburg, Germany.
Celine DregerDiv. Genetic Immunotherapy, Leibniz Institute for Immunotherapy, Regensburg, Germany.
Kathrin HammonDiv. Genetic Immunotherapy, Leibniz Institute for Immunotherapy, Regensburg, Germany.
Moritz ErteltInstitute for Drug Discovery, Faculty of Medicine, Leipzig University, Leipzig, Germany.
Clara T SchoederInstitute for Drug Discovery, Faculty of Medicine, Leipzig University, Leipzig, Germany.
Hólmfridur Rósa HalldórsdóttirDepartment of Health Technology, Technical University of Denmark, Kongens Lyngby, Denmark.
Carlos Rodriguez-PardoDepartment of Health Technology, Technical University of Denmark, Kongens Lyngby, Denmark.
Sine Reker HadrupDepartment of Health Technology, Technical University of Denmark, Kongens Lyngby, Denmark.
Simone Thomas *Div. Genetic Immunotherapy, Leibniz Institute for Immunotherapy, Regensburg, Germany.
Hinrich Abken *Div. Genetic Immunotherapy, Leibniz Institute for Immunotherapy, Regensburg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Adoptive therapy with CD19 chimeric antigen receptor (CAR) T cells is effective against B-cell malignancies; however, T-cell activation rapidly declines, increasing the risk of early leukemia relapses. To augment CD19 CAR T-cell functionality, we interfered with the physiological control of T-cell activation by a CAR that prevents the T cell's inherent CD30-CD30L interaction. Redirected by the bispecific CD30/CD19 CAR, T cells were superior to canonical CD19 CAR T cells in eliminating CD30

Indexed as

Antigens, CD19Immunotherapy, AdoptiveKi-1 AntigenLeukemia, B-CellLymphoma, B-CellReceptors, Chimeric AntigenT-LymphocytesCell Line, TumorHumansLymphocyte ActivationAntigens, CD19CD19 molecule, humanKi-1 AntigenReceptors, Chimeric AntigenCAR (chimeric antigen receptor)CD19CD30leukemialymphomaT cell

Identifiers

PMID42148107
PMCPMC13171528

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.