Evidence map›Paper›PMID 36044863›Full record

ArticleCell reports2022

Organoids capture tissue-specific innate lymphoid cell development in mice and humans.

Geraldine M Jowett, Emily Read, Luke B Roberts, Diana Coman, Marta Vilà González, Tomasz Zabinski, Umar Niazi, Rita Reis, Tung-Jui Trieu, Davide Danovi and 5 more

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

24 citing papers in PubMed, 33 citations in OpenAlex.

  1. Review
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  4. New developments and applications of human organoids.Nature reviews. Molecular cell biology · 2026
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  19. Group 3 innate lymphoid cells in intestinal health and disease.Nature reviews. Gastroenterology & hepatology · 2024
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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 at 3 institutions in 1 country.

Geraldine M JowettSchool for Immunology and Microbial Sciences, King's College London, London SE1 9RT, UK; Centre for Host Microbiome Interactions, King's College London, London SE1 9RT, UK; Centre for Craniofacial and Regenerative Biology, King's College London, London SE1 9RT, UK; Centre for Gene Therapy & Regenerative Medicine, King's College London, London SE1 9RT, UK; Wellcome Trust Cell Therapies and Regenerative Medicine Ph.D. Programme, London SE1 9RT, UK.
Emily ReadSchool for Immunology and Microbial Sciences, King's College London, London SE1 9RT, UK; Centre for Host Microbiome Interactions, King's College London, London SE1 9RT, UK; Centre for Gene Therapy & Regenerative Medicine, King's College London, London SE1 9RT, UK.
Luke B RobertsSchool for Immunology and Microbial Sciences, King's College London, London SE1 9RT, UK.
Diana ComanCentre for Host Microbiome Interactions, King's College London, London SE1 9RT, UK.
Marta Vilà GonzálezWellcome and MRC Cambridge Stem Cell Institute, Puddicombe Way, Cambridge CB2 0AW, UK; Department of Surgery, University of Cambridge and NIHR Cambridge Biomedical Research Centre, Hills Road, Cambridge CB2 0QQ, UK.
Tomasz ZabinskiSchool for Immunology and Microbial Sciences, King's College London, London SE1 9RT, UK.
Umar NiaziGuy's and St. Thomas' National Health Service Foundation Trust and King's College London National Institute for Health and Care Research Biomedical Research Centre Translational Bioinformatics Platform, Guy's Hospital, London SE1 9RT, UK.
Rita ReisSchool for Immunology and Microbial Sciences, King's College London, London SE1 9RT, UK.
Tung-Jui TrieuCentre for Host Microbiome Interactions, King's College London, London SE1 9RT, UK; Centre for Craniofacial and Regenerative Biology, King's College London, London SE1 9RT, UK.
Davide DanoviCentre for Craniofacial and Regenerative Biology, King's College London, London SE1 9RT, UK; bit.bio, Babraham Research Campus, The Dorothy Hodgkin Building, Cambridge CB22 3FH, UK.
Eileen GentlemanCentre for Craniofacial and Regenerative Biology, King's College London, London SE1 9RT, UK.
Ludovic VallierWellcome and MRC Cambridge Stem Cell Institute, Puddicombe Way, Cambridge CB2 0AW, UK; Department of Surgery, University of Cambridge and NIHR Cambridge Biomedical Research Centre, Hills Road, Cambridge CB2 0QQ, UK.
Michael A CurtisCentre for Host Microbiome Interactions, King's College London, London SE1 9RT, UK.
Graham M LordSchool for Immunology and Microbial Sciences, King's College London, London SE1 9RT, UK; Faculty of Biology, Medicine and Health, University of Manchester, Oxford Road, Manchester M13 9PL, UK.
Joana F NevesSchool for Immunology and Microbial Sciences, King's College London, London SE1 9RT, UK; Centre for Host Microbiome Interactions, King's College London, London SE1 9RT, UK. Electronic address: joana.pereira_das_neves@kcl.ac.uk.
King's College London · GBWellcome/MRC Cambridge Stem Cell Institute · GBNational Health Service · GB

Funding

Department of HealthMedical Research Council MC_PC_17230Medical Research Council MR/K002996/1Medical Research Council MR/M003493/1Medical Research Council MR/R024812/1Wellcome TrustWellcome Trust 091009Wellcome Trust 108874/B/15/ZWellcome Trust 204394/Z/16/Z
6 · The paper itself

Abstract

Organoid-based models of murine and human innate lymphoid cell precursor (ILCP) maturation are presented. First, murine intestinal and pulmonary organoids are harnessed to demonstrate that the epithelial niche is sufficient to drive tissue-specific maturation of all innate lymphoid cell (ILC) groups in parallel, without requiring subset-specific cytokine supplementation. Then, more complex human induced pluripotent stem cell (hiPSC)-based gut and lung organoid models are used to demonstrate that human epithelial cells recapitulate maturation of ILC from a stringent systemic human ILCP population, but only when the organoid-associated stromal cells are depleted. These systems offer versatile and reductionist models to dissect the impact of environmental and mucosal niche cues on ILC maturation. In the future, these could provide insight into how ILC activity and development might become dysregulated in chronic inflammatory diseases.

Indexed as

Induced Pluripotent Stem CellsOrganoidsAnimalsCell DifferentiationHumansImmunity, InnateImmunotherapyLymphocytesMiceCP: Developmental biologyCP: Immunologyepithelial organoidsinnate lymphoid cell developmentmucosal co-culturesstromal cells

Identifiers

PMID36044863
PMCPMC9638027
OpenAlexW4293574553

What OpenQuestion holds

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LicenceCC BY
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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.