Evidence map›Paper›PMID 39811682›Full record

ArticleMolecular therapy. Oncology2025

Enhancing NK cell-mediated tumor killing of B7-H6

Léxane Fournier, Paul Arras, Lukas Pekar, Harald Kolmar, Stefan Zielonka, Lars Toleikis, Stefan Becker

Abstract read
In one paragraph

Article in Molecular therapy. Oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Article
  3. 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

7 authors.

Léxane FournierEarly Protein Supply and Characterization, Merck Healthcare KGaA, 64293 Darmstadt, Germany.
Paul ArrasAntibody Discovery and Protein Engineering, Merck Healthcare KGaA, 64293 Darmstadt, Germany.
Lukas PekarAntibody Discovery and Protein Engineering, Merck Healthcare KGaA, 64293 Darmstadt, Germany.
Harald KolmarInstitute for Organic Chemistry and Biochemistry, Technical University of Darmstadt, 64287 Darmstadt, Germany.
Stefan ZielonkaInstitute for Organic Chemistry and Biochemistry, Technical University of Darmstadt, 64287 Darmstadt, Germany.
Lars ToleikisEarly Protein Supply and Characterization, Merck Healthcare KGaA, 64293 Darmstadt, Germany.
Stefan BeckerEarly Protein Supply and Characterization, Merck Healthcare KGaA, 64293 Darmstadt, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In this work, we report the discovery and engineering of allosteric variable domains of the heavy chain (VHHs) derived from camelid immunization targeting NKp30, an activating receptor on natural killer (NK) cells. The aim was to enhance NK cell-mediated killing capacities by identifying VHHs that do not compete with the natural ligand of NKp30:B7-H6, thereby maximizing the recognition of B7-H6

Indexed as

allosteric sitebispecific antibodiesbsAbscancer therapyDuoBodyEGFRMT: Regular Issuenatural-killer cell engagerNKCENKp30

Identifiers

PMID39811682
PMCPMC11730255

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.