Evidence map›Paper›PMID 42694115›Full record

ArticleFrontiers in immunology2026

Pre-treatment T cell features and immune-milieu characteristics shape treatment-induced exhaustion and resistance to Blinatumomab in B-cell acute lymphoblastic leukemia.

Francesco Corrado, Viktoria Blumenberg, Maryam Kazerani, Jan Wulf, Tobias Straub, Nora Philipp, Daniel Nixdorf, Amelie Muth, Giulia Rappa, Agnese Petrera and 7 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.

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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

17 authors.

Francesco CorradoLaboratory for Translational Cancer Immunology, LMU Gene Center, Munich, Germany.
Viktoria BlumenbergLaboratory for Translational Cancer Immunology, LMU Gene Center, Munich, Germany.
Maryam KazeraniLaboratory for Translational Cancer Immunology, LMU Gene Center, Munich, Germany.
Jan WulfLaboratory for Translational Cancer Immunology, LMU Gene Center, Munich, Germany.
Tobias StraubLaboratory for Translational Cancer Immunology, LMU Gene Center, Munich, Germany.
Nora PhilippLaboratory for Translational Cancer Immunology, LMU Gene Center, Munich, Germany.
Daniel NixdorfLaboratory for Translational Cancer Immunology, LMU Gene Center, Munich, Germany.
Amelie MuthLaboratory for Translational Cancer Immunology, LMU Gene Center, Munich, Germany.
Giulia RappaLaboratory for Translational Cancer Immunology, LMU Gene Center, Munich, Germany.
Agnese PetreraMetabolomics and Proteomics Core Facility, Helmholtz Center Munich - German Research Center for Environmental Health (GmbH), Munich, Germany.
Michaela ScheurerDepartment of Medicine III, LMU University Hospital, Ludwig Maximilian University (LMU) Munich, Munich, Germany.
Chang-Feng ChuTranslaTUM at Technical University of Munich, Munich, Germany.
Giulia MagnoLaboratory for Translational Cancer Immunology, LMU Gene Center, Munich, Germany.
Christina E ZielinskiDepartment of Infection Immunology, Leibniz-Institute for Natural Product Research and Infection Biology, Jena, Germany.
Michael von Bergwelt-BaildonDepartment of Medicine III, LMU University Hospital, Ludwig Maximilian University (LMU) Munich, Munich, Germany.
Marion SubkleweLaboratory for Translational Cancer Immunology, LMU Gene Center, Munich, Germany.
Veit BückleinLaboratory for Translational Cancer Immunology, LMU Gene Center, Munich, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Blinatumomab (Blina), a CD19×CD3 bispecific T cell engager, is approved for the treatment of B-cell precursor acute lymphoblastic leukemia (BCP-ALL), yet resistance remains a major challenge and the mechanisms driving treatment failure remain poorly understood. Methods: To define the immunological determinants of resistance, we performed longitudinal profiling of peripheral blood T cells and the immune milieu of 34 patients receiving Blina using flow cytometry (n=19), single-cell CITE-seq (n=13), Results: At baseline, Responders (R) were enriched for CD8 Conclusions: These findings indicate that post-Blina CD8

Indexed as

Antibodies, BispecificCD8-Positive T-LymphocytesDrug Resistance, NeoplasmPrecursor B-Cell Lymphoblastic Leukemia-LymphomaFemaleHumansMaleProteomicsT-Cell ExhaustionAntibodies, Bispecificblinatumomabacute B cell lymphoblastic leukemiamultiomic analysesproteomic analysissingle cell CITE sequencingT cell redirecting bispecific antibodies (bsAbs)

Identifiers

PMID42694115
PMCPMC13538086

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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.