Evidence map›Paper›PMID 42242923›Full record

ArticleLife science alliance2026

A "scan and stop" assay identifies CD40 and CD70 as selective regulators of T-cell arrest on APCs.

Vincent Gloe, Richard Schregle, Christoph Ratswohl, Jérémie Rossy

Abstract read
In one paragraph

Article in Life science alliance, 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

4 authors.

Vincent GloeInstitute of Cell Biology and Immunology Thurgau (BITG), University of Konstanz, Kreuzlingen, Switzerland.ORCID https://orcid.org/0009-0004-1223-0812
Richard SchregleInstitute of Cell Biology and Immunology Thurgau (BITG), University of Konstanz, Kreuzlingen, Switzerland.
Christoph RatswohlInstitute of Cell Biology and Immunology Thurgau (BITG), University of Konstanz, Kreuzlingen, Switzerland.ORCID https://orcid.org/0000-0001-5413-0730
Jérémie RossyInstitute of Cell Biology and Immunology Thurgau (BITG), University of Konstanz, Kreuzlingen, Switzerland jeremie.rossy@gmail.com.ORCID https://orcid.org/0000-0002-5128-5283

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

T-cell activation requires firm arrest on APCs, a process essential for effective clonal expansion and differentiation. Although the role of co-inhibitory signals and integrin-mediated adhesion in modulating T-cell arrest is established, the contribution of co-stimulatory molecules to this process remains poorly understood. Here, we developed a quantitative "scan and stop" assay using engineered CHO cells as minimalistic APCs to systematically assess the influence of co-stimulatory proteins on T-cell arrest. These APCs express only selected peptide-MHC complexes and co-stimulatory ligands, allowing controlled investigation of their roles in both naïve and experienced CD4

Indexed as

Antigen-Presenting CellsCD27 LigandCD40 AntigensT-LymphocytesAnimalsCD40 LigandCD4-Positive T-LymphocytesCD8-Positive T-LymphocytesCHO CellsCricetulusHumansLymphocyte ActivationCD27 LigandCD40 AntigensCD40 Ligand

Identifiers

PMID42242923
PMCPMC13237129

What OpenQuestion holds

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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.