Evidence map›Paper›PMID 37591933›Full record

ArticleNature nanotechnology2023

Programmable multispecific DNA-origami-based T-cell engagers.

Klaus F Wagenbauer, Nhi Pham, Adrian Gottschlich, Benjamin Kick, Viktorija Kozina, Christopher Frank, Daniela Trninic, Pierre Stömmer, Ruth Grünmeier, Emanuele Carlini and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Nature nanotechnology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
22.5field-weighted citation impact, top 1% of its field
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

39 citing papers in PubMed, 98 citations in OpenAlex.

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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

14 authors at 4 institutions in 1 country.

Klaus F Wagenbauer *Department of Biosciences, School of Natural Sciences, Technical University of Munich, Garching, Germany.
Nhi Pham *Department of Biosciences, School of Natural Sciences, Technical University of Munich, Garching, Germany.
Adrian Gottschlich *Division of Clinical Pharmacology, University Hospital, LMU Munich, Member of the German Center for Lung Research (DZL), Munich, Germany.ORCID 0000-0002-2898-4182
Benjamin Kick *Department of Biosciences, School of Natural Sciences, Technical University of Munich, Garching, Germany.
Viktorija KozinaDepartment of Biosciences, School of Natural Sciences, Technical University of Munich, Garching, Germany.
Christopher FrankDepartment of Biosciences, School of Natural Sciences, Technical University of Munich, Garching, Germany.
Daniela TrninicDepartment of Biosciences, School of Natural Sciences, Technical University of Munich, Garching, Germany.
Pierre StömmerDepartment of Biosciences, School of Natural Sciences, Technical University of Munich, Garching, Germany.ORCID 0000-0003-1683-3392
Ruth GrünmeierDivision of Clinical Pharmacology, University Hospital, LMU Munich, Member of the German Center for Lung Research (DZL), Munich, Germany.ORCID 0000-0002-9044-3600
Emanuele CarliniDivision of Clinical Pharmacology, University Hospital, LMU Munich, Member of the German Center for Lung Research (DZL), Munich, Germany.
Christina Angeliki TsiveriotiDivision of Clinical Pharmacology, University Hospital, LMU Munich, Member of the German Center for Lung Research (DZL), Munich, Germany.
Sebastian KoboldDivision of Clinical Pharmacology, University Hospital, LMU Munich, Member of the German Center for Lung Research (DZL), Munich, Germany. sebastian.kobold@med.uni-muenchen.de.ORCID 0000-0002-5612-4673
Jonas J FunkeDepartment of Biosciences, School of Natural Sciences, Technical University of Munich, Garching, Germany. jonasfunke@mytum.de.
Hendrik DietzDepartment of Biosciences, School of Natural Sciences, Technical University of Munich, Garching, Germany. dietz@tum.de.ORCID 0000-0003-1270-3662
Technical University of Munich · DEGerman Center for Lung Research · DEGerman Cancer Research Center · DELMU Klinikum · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multispecific antibodies have emerged as versatile therapeutic agents, and therefore, approaches to optimize and streamline their design and assembly are needed. Here we report on the modular and programmable assembly of IgG antibodies, F(ab) and scFv fragments on DNA origami nanocarriers. We screened 105 distinct quadruplet antibody variants in vitro for the ability to activate T cells in the presence of target cells. T-cell engagers were identified, which in vitro showed the specific and efficient T-cell-mediated lysis of five distinct target cell lines. We used these T-cell engagers to target and lyse tumour cells in vivo in a xenograft mouse tumour model. Our approach enables the rapid generation, screening and testing of bi- and multispecific antibodies to facilitate preclinical pharmaceutical development from in vitro discovery to in vivo proof of concept.

Indexed as

NeoplasmsT-LymphocytesAnimalsDNAHumansImmunoglobulin GMiceDNAImmunoglobulin G

Identifiers

PMID37591933
PMCPMC10656288
OpenAlexW4385955237

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.