Evidence map›Paper›PMID 41402230›Full record

ArticlemAbs2026

P329G-engager: a universal mix & match antibody-based adaptor platform for cancer immunotherapy.

Marlena Surowka, Diana Darowski, Idil Hutter-Karakoc, Christina Claus, Claudia Ferrara-Koller, Anne Freimoser-Grundschober, Thomas Hofer, Johannes Sam, Reto Gianotti, Andrzej Sobieniecki and 7 more

Abstract read
In one paragraph

Article in mAbs, 2026. 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. Article
  2. T cell engagers in autoimmune diseases.Nature reviews. Immunology · 2026
    Review
  3. 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

17 authors.

Marlena SurowkaRoche Pharma Research and Early Development, Roche Innovation Center Zurich, Schlieren, Switzerland.ORCID 0009-0007-2113-9692
Diana DarowskiRoche Pharma Research and Early Development, Roche Innovation Center Zurich, Schlieren, Switzerland.
Idil Hutter-KarakocRoche Pharma Research and Early Development, Roche Innovation Center Zurich, Schlieren, Switzerland.
Christina ClausRoche Pharma Research and Early Development, Roche Innovation Center Zurich, Schlieren, Switzerland.
Claudia Ferrara-KollerRoche Pharma Research and Early Development, Roche Innovation Center Zurich, Schlieren, Switzerland.
Anne Freimoser-GrundschoberRoche Pharma Research and Early Development, Roche Innovation Center Zurich, Schlieren, Switzerland.
Thomas HoferRoche Pharma Research and Early Development, Roche Innovation Center Zurich, Schlieren, Switzerland.
Johannes SamRoche Pharma Research and Early Development, Roche Innovation Center Zurich, Schlieren, Switzerland.
Reto GianottiRoche Pharma Research and Early Development, Roche Innovation Center Zurich, Schlieren, Switzerland.
Andrzej SobienieckiRoche Pharma Research and Early Development, Roche Innovation Center Zurich, Schlieren, Switzerland.
Denis AssisiRoche Pharma Research and Early Development, Roche Innovation Center Zurich, Schlieren, Switzerland.
John ChallierRoche Pharma Research and Early Development, Roche Innovation Center Zurich, Schlieren, Switzerland.
Stephane LeclairRoche Pharma Research and Early Development, Roche Innovation Center Munich, Penzberg, Germany.
Ekkehard MössnerRoche Pharma Research and Early Development, Roche Innovation Center Zurich, Schlieren, Switzerland.
Maria AmannRoche Pharma Research and Early Development, Roche Innovation Center Zurich, Schlieren, Switzerland.
Pablo UmañaRoche Pharma Research and Early Development, Roche Innovation Center Zurich, Schlieren, Switzerland.
Christian KleinRoche Pharma Research and Early Development, Roche Innovation Center Zurich, Schlieren, Switzerland.ORCID 0000-0001-7594-7280

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Targeting various combinations of tumor antigens and immune cell receptors is of increasing importance in antibody-based cancer immunotherapy. Here, we present a novel modular P329G-engager platform that enables rapid combination of primary tumor-targeting and secondary immune effector antibodies. The platform utilizes two antibodies, each selected from: 1) a set of tumor-targeting adaptor antibodies, bearing P329G mutations in the Fc region, and 2) a set of P329G-targeting (bispecific) cell engagers, including innate and T cell engagers, costimulators and immunocytokines. Specifically, upon defining a tumor-associated cell surface target, a primary adaptor - tumor antigen-binding IgG1 antibody with Fc-silencing P329G L234A L235A mutations - is administered. Subsequently, a secondary antibody recognizing the P329G mutation is chosen from a panel of effector cell engagers with different modes of action - ADCC-competent P329G-innate cell engagers (P329G-ICE), P329G-T cell bispecifics (P329G-TCB), P329G-costimulators (P329G-CD28/4-1BBL), or P329G-immunocytokine (P329G-IL2v).

Indexed as

Antibodies, BispecificImmunotherapyNeoplasmsAnimalsAntibody-Dependent Cell CytotoxicityAntigens, NeoplasmCell Line, TumorFemaleHumansImmunoglobulin GMiceMutationXenograft Model Antitumor AssaysAntibodies, BispecificAntigens, NeoplasmImmunoglobulin Gadaptor antibodyantigen-agnosticcancer immunotherapymix & match therapyoff-the-shelfTCBT cell engager

Identifiers

PMID41402230
PMCPMC12710928

What OpenQuestion holds

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LicenceCC BY-NC
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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.