Evidence map›Paper›PMID 37986877›Full record

ArticlebioRxiv : the preprint server for biology2023

A spatial human thymus cell atlas mapped to a continuous tissue axis.

Nadav Yayon, Veronika R Kedlian, Lena Boehme, Chenqu Suo, Brianna Wachter, Rebecca T Beuschel, Oren Amsalem, Krzysztof Polanski, Simon Koplev, Elizabeth Tuck and 35 more

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed, 19 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

45 authors at 11 institutions in 4 countries.

Nadav YayonWellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.ORCID 0000-0002-7034-0524
Veronika R KedlianWellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.ORCID 0000-0001-6563-0829
Lena BoehmeGhent University, Department of Diagnostic Sciences, Ghent, Belgium.ORCID 0000-0001-7593-7533
Chenqu SuoWellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.ORCID 0000-0002-8813-0875
Brianna WachterNational Institute of Allergy and Infectious Diseases, National Institutes of Health (NIH), Laboratory of Clinical Immunology and Microbiology, Division of Intramural Research, Bethesda, MD, United States.ORCID 0000-0002-2950-2683
Rebecca T BeuschelNational Institute of Allergy and Infectious Diseases, NIH, Lymphocyte Biology Section and Center for Advanced Tissue Imaging, Bethesda, MD, United States.ORCID 0000-0002-3882-457X
Oren AmsalemBeth Israel Deaconess Medical Center, Harvard Medical School, Division of Endocrinology, Diabetes and Metabolism, Boston, MA, United States.ORCID 0000-0002-8070-0378
Krzysztof PolanskiWellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.ORCID 0000-0002-2586-9576
Simon KoplevWellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.ORCID 0000-0002-8586-5614
Elizabeth TuckWellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.
Emma DannWellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.ORCID 0000-0002-7400-7438
Jolien Van HulleGhent University, Department of Diagnostic Sciences, Ghent, Belgium.ORCID 0000-0001-8844-3700
Shani PereraWellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.ORCID 0000-0001-8021-2078
Tom PuttemanGhent University, Department of Diagnostic Sciences, Ghent, Belgium.ORCID 0000-0001-5098-4317
Alexander V PredeusWellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.ORCID 0000-0002-2750-1599
Monika DabrowskaWellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.
Laura RichardsonWellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.
Catherine TudorWellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.ORCID 0000-0003-2093-9683
Alexandra Y KreinsGreat Ormond Street Hospital for Children NHS Foundation Trust, Department of Immunology and Gene Therapy, London, United Kingdom.ORCID 0000-0001-8748-5837
Justin EngelbertNewcastle University, Biosciences Institute, Faculty of Medical Sciences, Newcastle upon Tyne, United Kingdom.
Emily StephensonNewcastle University, Biosciences Institute, Faculty of Medical Sciences, Newcastle upon Tyne, United Kingdom.ORCID 0000-0002-4244-4019
Vitalii KleshchevnikovWellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.ORCID 0000-0001-9110-7441
Fabrizio De RitaFreeman Hospital, Department of Adult Congenital Heart Disease and Paediatric Cardiology/Cardiothoracic Surgery, Newcastle upon Tyne, United Kingdom.
David CrosslandFreeman Hospital, Department of Adult Congenital Heart Disease and Paediatric Cardiology/Cardiothoracic Surgery, Newcastle upon Tyne, United Kingdom.
Marita BosticardoNational Institute of Allergy and Infectious Diseases, National Institutes of Health (NIH), Laboratory of Clinical Immunology and Microbiology, Division of Intramural Research, Bethesda, MD, United States.ORCID 0000-0002-1771-4523
Francesca PalaNational Institute of Allergy and Infectious Diseases, National Institutes of Health (NIH), Laboratory of Clinical Immunology and Microbiology, Division of Intramural Research, Bethesda, MD, United States.
Elena PrigmoreWellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.
Nana-Jane ChipampeWellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.
Martin PreteWellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.ORCID 0000-0002-5946-821X
Lijiang FeiWellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.
Ken ToWellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.ORCID 0000-0001-9262-7190
Roger A BarkerUniversity of Cambridge, John van Geest Centre for Brain Repair, Department of Clinical Neurosciences and Wellcome-MRC Cambridge Stem Cell Institute, Cambridge, United Kingdom.
Xiaoling HeUniversity of Cambridge, John van Geest Centre for Brain Repair, Department of Clinical Neurosciences and Wellcome-MRC Cambridge Stem Cell Institute, Cambridge, United Kingdom.
Filip Van NieuwerburghGhent University, Laboratory of Pharmaceutical Biotechnology, Ghent, Belgium.ORCID 0000-0001-8815-5485
Omer BayraktarWellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.
Minal PatelWellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.
Graham E DaviesGreat Ormond Street Hospital for Children NHS Foundation Trust, Department of Immunology and Gene Therapy, London, United Kingdom.
Muzlifah A HaniffaWellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.ORCID 0000-0002-3927-2084
Virginie UhlmannEuropean Molecular Biology Laboratory, European Bioinformatics Institute, Cambridge, United Kingdom.ORCID 0000-0002-2859-9241
Luigi D NotarangeloNational Institute of Allergy and Infectious Diseases, National Institutes of Health (NIH), Laboratory of Clinical Immunology and Microbiology, Division of Intramural Research, Bethesda, MD, United States.ORCID 0000-0002-8335-0262
Ronald N GermainNational Institute of Allergy and Infectious Diseases, NIH, Lymphocyte Biology Section and Center for Advanced Tissue Imaging, Bethesda, MD, United States.
Andrea J RadtkeNational Institute of Allergy and Infectious Diseases, NIH, Lymphocyte Biology Section and Center for Advanced Tissue Imaging, Bethesda, MD, United States.ORCID 0000-0003-4379-8967
John C MarioniEuropean Molecular Biology Laboratory, European Bioinformatics Institute, Cambridge, United Kingdom.ORCID 0000-0001-9092-0852
Tom TaghonGhent University, Department of Diagnostic Sciences, Ghent, Belgium.ORCID 0000-0002-5781-0288
Sarah A TeichmannWellcome Sanger Institute, Cellular Genetics, Cambridge, United Kingdom.ORCID 0000-0002-6294-6366
Wellcome Sanger Institute · GBNational Institutes of Health · USGhent University Hospital · BEEuropean Bioinformatics Institute · GBFreeman Hospital · GBGreat Ormond Street Hospital for Children NHS Foundation Trust · GBNewcastle University · GBWellcome/MRC Cambridge Stem Cell Institute · GBBeth Israel Deaconess Medical Center · USGhent University · BEUniversity of Cambridge · GB

Funding

Wellcome Trust
6 · The paper itself

Abstract

T cells develop from circulating precursors, which enter the thymus and migrate throughout specialised sub-compartments to support maturation and selection. This process starts already in early fetal development and is highly active until the involution of the thymus in adolescence. To map the micro-anatomical underpinnings of this process in pre- vs. post-natal states, we undertook a spatially resolved analysis and established a new quantitative morphological framework for the thymus, the Cortico-Medullary Axis. Using this axis in conjunction with the curation of a multimodal single-cell, spatial transcriptomics and high-resolution multiplex imaging atlas, we show that canonical thymocyte trajectories and thymic epithelial cells are highly organised and fully established by post-conception week 12, pinpoint TEC progenitor states, find that TEC subsets and peripheral tissue genes are associated with Hassall's Corpuscles and uncover divergence in the pace and drivers of medullary entry between CD4 vs. CD8 T cell lineages. These findings are complemented with a holistic toolkit for spatial analysis and annotation, providing a basis for a detailed understanding of T lymphocyte development.

Identifiers

PMID37986877
PMCPMC10659407
OpenAlexW4387998733

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.