Evidence map›Paper›PMID 36543915›Full record

ArticleNature genetics2023

A spatially resolved atlas of the human lung characterizes a gland-associated immune niche.

Elo Madissoon, Amanda J Oliver, Vitalii Kleshchevnikov, Anna Wilbrey-Clark, Krzysztof Polanski, Nathan Richoz, Ana Ribeiro Orsi, Lira Mamanova, Liam Bolt, Rasa Elmentaite and 30 more

Open access · hybridAbstract read
In one paragraph

Article in Nature genetics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 157 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
157citing papers in PubMed, 1 pooled it
15.9field-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

157 citing papers in PubMed, 1 synthesis or guideline pooled it, 207 citations in OpenAlex.

  1. Pooled it
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  3. Article
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  5. Article
  6. Accurately Predicting Cell Type Abundance from Spatial Histology Image Through HPCell.Interdisciplinary sciences, computational life sciences · 2026
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97 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

40 authors at 8 institutions in 4 countries.

Elo Madissoon *Wellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.
Amanda J Oliver *Wellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.ORCID http://orcid.org/0000-0003-1690-9027
Vitalii KleshchevnikovWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.
Anna Wilbrey-ClarkWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.
Krzysztof PolanskiWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.ORCID http://orcid.org/0000-0002-2586-9576
Nathan RichozMolecular Immunity Unit, University of Cambridge Department of Medicine, MRC Laboratory of Molecular Biology, Francis Crick Ave, Cambridge, UK.
Ana Ribeiro OrsiWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.ORCID http://orcid.org/0000-0002-4939-1423
Lira MamanovaWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.ORCID http://orcid.org/0000-0003-1463-8622
Liam BoltWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.
Rasa ElmentaiteWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.ORCID http://orcid.org/0000-0001-7366-5466
J Patrick PettWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.ORCID http://orcid.org/0000-0002-5249-444X
Ni HuangWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.
Chuan XuWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.
Peng HeWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.ORCID http://orcid.org/0000-0002-2457-3554
Monika DabrowskaWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.
Sophie PritchardWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.
Liz TuckWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.ORCID http://orcid.org/0000-0002-1837-7549
Elena PrigmoreWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.ORCID http://orcid.org/0000-0001-8870-0316
Shani PereraWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.
Andrew KnightsWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.
Agnes OszlancziWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.
Adam HunterWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.
Sara F VieiraWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.ORCID http://orcid.org/0000-0002-1021-3021
Minal PatelWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.
Rik G H LindeboomWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.ORCID http://orcid.org/0000-0002-3660-504X
Lia S CamposWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.
Kazuhiko MatsuoKindai University Faculty of Pharmacy, Higashi-osaka, Japan.
Takashi NakayamaKindai University Faculty of Pharmacy, Higashi-osaka, Japan.ORCID http://orcid.org/0000-0002-8493-899X
Masahiro YoshidaUCL Respiratory, Division of Medicine, University College London Hospitals NHS Foundation Trust, London, UK.ORCID http://orcid.org/0000-0002-3521-5322
Kaylee B WorlockUCL Respiratory, Division of Medicine, University College London Hospitals NHS Foundation Trust, London, UK.ORCID http://orcid.org/0000-0002-5656-7634
Marko Z NikolićUCL Respiratory, Division of Medicine, University College London Hospitals NHS Foundation Trust, London, UK.ORCID http://orcid.org/0000-0001-6304-6848
Nikitas GeorgakopoulosDepartment of Surgery, University of Cambridge, and Cambridge NIHR Biomedical Research Centre, Cambridge, UK.ORCID http://orcid.org/0000-0002-1879-6583
Krishnaa T MahbubaniDepartment of Surgery, University of Cambridge, and Cambridge NIHR Biomedical Research Centre, Cambridge, UK.ORCID http://orcid.org/0000-0002-1327-2334
Kourosh Saeb-ParsyDepartment of Surgery, University of Cambridge, and Cambridge NIHR Biomedical Research Centre, Cambridge, UK.ORCID http://orcid.org/0000-0002-0633-3696
Omer Ali BayraktarWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.ORCID http://orcid.org/0000-0001-6055-277X
Menna R ClatworthyWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.
Oliver StegleWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.
Natsuhiko KumasakaWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK.ORCID http://orcid.org/0000-0002-3557-0375
Sarah A TeichmannWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK. st9@sanger.ac.uk.ORCID http://orcid.org/0000-0002-6294-6366
Kerstin B MeyerWellcome Sanger Institute, Wellcome Genome Campus, Cambridge, UK. km16@sanger.ac.uk.ORCID http://orcid.org/0000-0001-5906-1498
Wellcome Sanger Institute · GBUniversity of Cambridge · GBUniversity College London Hospitals NHS Foundation Trust · GBEuropean Bioinformatics Institute · GBKindai University · JPMRC Laboratory of Molecular Biology · GBGerman Cancer Research Center · DEUniversidade de São Paulo · BR

Funding

Medical Research Council MR/5005579/1Medical Research Council MR/S005579/1Medical Research Council MR/W00111X/1Wellcome Trust 206194Wellcome Trust 211276Wellcome Trust WT211276/Z/18/Z
6 · The paper itself

Abstract

Single-cell transcriptomics has allowed unprecedented resolution of cell types/states in the human lung, but their spatial context is less well defined. To (re)define tissue architecture of lung and airways, we profiled five proximal-to-distal locations of healthy human lungs in depth using multi-omic single cell/nuclei and spatial transcriptomics (queryable at lungcellatlas.org ). Using computational data integration and analysis, we extend beyond the suspension cell paradigm and discover macro and micro-anatomical tissue compartments including previously unannotated cell types in the epithelial, vascular, stromal and nerve bundle micro-environments. We identify and implicate peribronchial fibroblasts in lung disease. Importantly, we discover and validate a survival niche for IgA plasma cells in the airway submucosal glands (SMG). We show that gland epithelial cells recruit B cells and IgA plasma cells, and promote longevity and antibody secretion locally through expression of CCL28, APRIL and IL-6. This new 'gland-associated immune niche' has implications for respiratory health.

Indexed as

LungRespiratory MucosaB-LymphocytesEpithelial CellsHumansImmunoglobulin AImmunoglobulin A

Identifiers

PMID36543915
PMCPMC9839452
OpenAlexW4312094540

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.