Evidence map›Paper›PMID 40250867›Full record

ArticleJournal for immunotherapy of cancer2025

Novel PD-1-targeted, activity-optimized IL-15 mutein SOT201 acting in cis provides antitumor activity superior to PD1-IL2v.

Hana Matuskova, Pavel Marasek, Vladyslav Mazhara, Ekaterina Simonova, Lucie Kosinova, Petr Danek, Klara Danova, Katerina Sajnerova, Iva Malatova, Klara Hrabankova and 17 more

Abstract read
In one paragraph

Article in Journal for immunotherapy of cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Review
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

27 authors.

Hana MatuskovaSOTIO Biotech a.s, Prague, Czech Republic.
Pavel MarasekSOTIO Biotech a.s, Prague, Czech Republic.
Vladyslav MazharaLaboratory of Tumor Immunology, Institute of Microbiology Czech Academy of Sciences, Prague, Czech Republic.
Ekaterina SimonovaSOTIO Biotech a.s, Prague, Czech Republic.
Lucie KosinovaSOTIO Biotech a.s, Prague, Czech Republic.
Petr DanekSOTIO Biotech a.s, Prague, Czech Republic.
Klara DanovaSOTIO Biotech a.s, Prague, Czech Republic.
Katerina SajnerovaSOTIO Biotech a.s, Prague, Czech Republic.
Iva MalatovaSOTIO Biotech a.s, Prague, Czech Republic.
Klara HrabankovaSOTIO Biotech a.s, Prague, Czech Republic.
Denise GrecoSOTIO Biotech a.s, Prague, Czech Republic.
Ondrej MartinecSOTIO Biotech a.s, Prague, Czech Republic.
Matej FabisikSOTIO Biotech a.s, Prague, Czech Republic.
Nada PodzimkovaSOTIO Biotech a.s, Prague, Czech Republic.
Kamila HladikovaSOTIO Biotech a.s, Prague, Czech Republic.
Katerina BehalovaLaboratory of Tumor Immunology, Institute of Microbiology Czech Academy of Sciences, Prague, Czech Republic.
Zuzana AntosovaSOTIO Biotech a.s, Prague, Czech Republic.
Milada SirovaLaboratory of Tumor Immunology, Institute of Microbiology Czech Academy of Sciences, Prague, Czech Republic.
Romana MikyskovaLaboratory of Immunological and Tumor models, Institute of Molecular Genetics Czech Academy of Sciences, Prague, Czech Republic.
Milan ReinisLaboratory of Immunological and Tumor models, Institute of Molecular Genetics Czech Academy of Sciences, Prague, Czech Republic.
Marek KovarLaboratory of Tumor Immunology, Institute of Microbiology Czech Academy of Sciences, Prague, Czech Republic.ORCID http://orcid.org/0000-0002-6602-1678
David BéchardCytune Pharma S.A.S, Nantes, France.
Ulrich MoebiusSOTIO Biotech a.s, Prague, Czech Republic.
Lenka Palova JelinkovaSOTIO Biotech a.s, Prague, Czech Republic.
Radek SpisekSOTIO Biotech a.s, Prague, Czech Republic.
Martin SteegmaierSOTIO Biotech a.s, Prague, Czech Republic.
Irena AdkinsSOTIO Biotech a.s, Prague, Czech Republic adkins@sotio.com.ORCID http://orcid.org/0009-0004-6714-8736

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSOT201 and its murine surrogate mSOT201 are novel cis-acting immunocytokines consisting of a humanized/murinized/, Fc-silenced anti-programmed cell death protein 1 (PD-1) monoclonal antibody (mAb) fused to an attenuated human interleukin (IL)-15 and the IL-15Rα sushi+ domain. Murine mPD1-IL2v is a conjugate of a murinized, Fc silenced anti-PD-1 mAb bearing human IL-2 with abolished IL-2Rα binding. These immunocytokines spatiotemporally reinvigorate PD-1

methodsHuman peripheral blood mononuclear cell and cell lines were used to evaluate cis/trans activity of SOT201. Anti-PD-1 mAb responsive (MC38, CT26) and resistant (B16F10, CT26 STK11 KO) mouse tumor models were used to determine the anticancer efficacy, and the underlying immune cell activity was analyzed via single-cell RNA sequencing and flow cytometry. The expansion of tumor antigen-specific CD8

resultsSOT201 delivers attenuated IL-15 to PD-1

conclusionsSOT201 represents a promising therapeutic candidate that preferentially targets PD-1

Indexed as

Interleukin-15Programmed Cell Death 1 ReceptorAnimalsCD8-Positive T-LymphocytesCell Line, TumorFemaleHumansImmune Checkpoint InhibitorsMiceImmune Checkpoint InhibitorsInterleukin-15PDCD1 protein, humanProgrammed Cell Death 1 ReceptorCytokineImmune Checkpoint InhibitorImmunotherapyT cellTumor microenvironment - TME

Identifiers

PMID40250867
PMCPMC12007054

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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.