Evidence map›Paper›PMID 41152624›Full record

ArticleNature biotechnology2026

A single-chain derivative of an integrin-activating antibody potentiates organoid growth in Matrigel and collagen hydrogels.

Wim B M de Lau, Joost J A P M Wijnakker, Gijs J F van Son, Daniel Krueger, Daisong Wang, Matthijs S Abendroth, Robin Schreurs, Claudia Y Janda, Fenna L H van Rijt, Benjamin J P Chalopin and 5 more

Abstract read
In one paragraph

Article in Nature biotechnology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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

9 citing papers in PubMed.

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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

15 authors.

Wim B M de Lau *Oncode Institute, Hubrecht Institute, Royal Netherlands Academy of Arts and Science (KNAW) and UMC, Utrecht, The Netherlands.
Joost J A P M Wijnakker *Oncode Institute, Hubrecht Institute, Royal Netherlands Academy of Arts and Science (KNAW) and UMC, Utrecht, The Netherlands.
Gijs J F van SonOncode Institute, Princess Maxima Center of Pediatric Oncology, Utrecht, The Netherlands.ORCID http://orcid.org/0000-0003-0572-3243
Daniel KruegerOncode Institute, Hubrecht Institute, Royal Netherlands Academy of Arts and Science (KNAW) and UMC, Utrecht, The Netherlands.ORCID http://orcid.org/0000-0003-1139-7755
Daisong WangOncode Institute, Hubrecht Institute, Royal Netherlands Academy of Arts and Science (KNAW) and UMC, Utrecht, The Netherlands.
Matthijs S AbendrothOncode Institute, Hubrecht Institute, Royal Netherlands Academy of Arts and Science (KNAW) and UMC, Utrecht, The Netherlands.ORCID http://orcid.org/0009-0004-4350-3449
Robin SchreursOncode Institute, Hubrecht Institute, Royal Netherlands Academy of Arts and Science (KNAW) and UMC, Utrecht, The Netherlands.
Claudia Y JandaOncode Institute, Princess Maxima Center of Pediatric Oncology, Utrecht, The Netherlands.ORCID http://orcid.org/0000-0002-3307-2559
Fenna L H van RijtOncode Institute, Princess Maxima Center of Pediatric Oncology, Utrecht, The Netherlands.
Benjamin J P ChalopinOncode Institute, Princess Maxima Center of Pediatric Oncology, Utrecht, The Netherlands.
Emma BokobzaOncode Institute, Princess Maxima Center of Pediatric Oncology, Utrecht, The Netherlands.
Johan H van EsOncode Institute, Hubrecht Institute, Royal Netherlands Academy of Arts and Science (KNAW) and UMC, Utrecht, The Netherlands.
Timothy A SpringerHarvard Medical School, Boston Children's Hospital, Boston, MA, USA.ORCID http://orcid.org/0000-0001-6627-2904
Arnoud SonnenbergDivision of Cell Biology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
Hans CleversOncode Institute, Hubrecht Institute, Royal Netherlands Academy of Arts and Science (KNAW) and UMC, Utrecht, The Netherlands. h.clevers@hubrecht.eu.ORCID http://orcid.org/0000-0002-3077-5582

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Current methods of culturing human epithelial organoids from adult stem cells may not be compatible with clinical applications as they rely on xenogeneic, chemically undefined or non-standardized components such as the basement membrane extract Matrigel. Matrigel provides a source of extracellular matrix molecules, including laminins and collagen IV, which interact with β1 integrins expressed on organoid cells. Here we describe a single-chain (sc) version of antibody TS2/16 that allosterically activates integrin β1 function in organoids. The addition of monomeric scTS2/16 to organoid medium results in up to a fivefold increase in the yield of all gastrointestinal organoids grown in Matrigel. Moreover, scTS2/16 supports a six- to sevenfold increase in the yield of these organoids when cultured in collagen I hydrogels, both in 3D and 2D. Collagen I is well defined, available in clinical-grade formulations and, when combined with scTS2/16, may support the clinical application of epithelial organoids derived from gastrointestinal tissues and other epithelial sources.

Indexed as

CollagenHydrogelsIntegrin beta1LamininOrganoidsProteoglycansDrug CombinationsHumansCollagenDrug CombinationsHydrogelsIntegrin beta1LamininmatrigelProteoglycans

Identifiers

PMID41152624
PMCPMC13654809

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.