Evidence map›Paper›PMID 42253710›Full record

ArticleJournal of extracellular biology2026

Single-EV Analyses Require Rigorous Antibody Qualification: PD-L1 Profiling in Cell Models and Patient Plasma.

Tobias Tertel, Fabiola Nardi Bauer, Oumaima Stambouli, Sabine Kasimir-Bauer, Corinna Keup, Stephan Lang, Ali Sak, Martin Stuschke, Tienush Rassaf, Martin Schuler and 3 more

Abstract read
In one paragraph

Article in Journal of extracellular biology, 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

13 authors.

Tobias TertelInstitute for Transfusion Medicine University Hospital Essen University of Duisburg-Essen Essen Germany.ORCID https://orcid.org/0000-0001-8659-8610
Fabiola Nardi BauerInstitute for Transfusion Medicine University Hospital Essen University of Duisburg-Essen Essen Germany.
Oumaima StambouliInstitute for Transfusion Medicine University Hospital Essen University of Duisburg-Essen Essen Germany.
Sabine Kasimir-BauerDepartment of Gynaecology and Obstetrics University Hospital Essen University of Duisburg-Essen Germany.
Corinna KeupDepartment of Gynaecology and Obstetrics University Hospital Essen University of Duisburg-Essen Germany.ORCID https://orcid.org/0000-0003-3525-7511
Stephan LangDepartment of Oto-Rhino-Laryngology University Hospital Essen University of Duisburg-Essen Germany.
Ali SakDepartment of Radiotherapy University Hospital Essen University of Duisburg-Essen Essen Germany.
Martin StuschkeDepartment of Radiotherapy University Hospital Essen University of Duisburg-Essen Essen Germany.
Tienush RassafDepartment of Cardiology and Vascular Medicine West German Heart- and Vascular Center University Hospital Essen University of Duisburg-Essen Germany.
Martin SchulerDepartment of Medical Oncology West German Cancer Center University Hospital Essen University of Duisburg-Essen Essen Germany.
Stefan Kasper-VirchowDepartment of Medical Oncology West German Cancer Center University Hospital Essen University of Duisburg-Essen Essen Germany.
Bernd GiebelInstitute for Transfusion Medicine University Hospital Essen University of Duisburg-Essen Essen Germany.
Alexander SchrammDepartment of Medical Oncology West German Cancer Center University Hospital Essen University of Duisburg-Essen Essen Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Imaging flow cytometry (IFCM) has emerged as a powerful method for high-throughput phenotyping of small extracellular vesicles (sEVs) at single-vesicle resolution. However, the reliability and sensitivity of IFCM critically depend on the performance of the antibodies used. In this study, we systematically compared several commercially available anti-PD-L1 antibodies for their ability to detect PD-L1-positive sEVs. Despite being derived from the same clone, antibodies from different manufacturers showed striking differences in labelling efficiency. These findings demonstrate that antibody validation for cellular targets does not ensure suitability for single-EV analysis and underscore the need for rigorous, application-specific qualification. To address this, we developed a robust IFCM workflow in full alignment with MIFlowCyt-EV reporting standards. Using a qualified anti-PD-L1 antibody, we achieved reproducible detection of PD-L1

Indexed as

antibody validationcancer plasmaextracellular vesiclesimaging flow cytometryPD‐L1single‐vesicle analysis

Identifiers

PMID42253710
PMCPMC13240509

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Registered trials

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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.