Evidence map›Paper›PMID 35549406›Full record

ArticleScience (New York, N.Y.)2022

Cross-tissue immune cell analysis reveals tissue-specific features in humans.

C Domínguez Conde, C Xu, L B Jarvis, D B Rainbow, S B Wells, T Gomes, S K Howlett, O Suchanek, K Polanski, H W King and 31 more

Open access · bronzeAbstract read
In one paragraph

Article in Science (New York, N.Y.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 721 papers.

0numbers the graph read from it
0cells of the map it votes in
721citing papers in PubMed
86.5field-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

721 citing papers in PubMed, 1,068 citations in OpenAlex.

  1. Trial
  2. B-Cell Aware Analysis of Single-Cell Transcriptomics Data.Methods in molecular biology (Clifton, N.J.) · 2027
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  17. celltypeEnrich: a consensus-based scRNA-seq cluster annotation tool.bioRxiv : the preprint server for biology · 2026
    Article
  18. Article
  19. A Gene-Program Architecture of Mouse T cells.bioRxiv : the preprint server for biology · 2026
    Article
  20. Article

661 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

41 authors at 7 institutions in 2 countries.

C Domínguez Conde *Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.ORCID 0000-0002-8684-4655
C Xu *Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.ORCID 0000-0002-6265-999X
L B Jarvis *Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.ORCID 0000-0002-5760-0125
D B Rainbow *Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.ORCID 0000-0003-4931-3289
S B Wells *Department of Systems Biology, Columbia University Irving Medical Center, New York, NY, USA.ORCID 0000-0001-5428-0683
T GomesWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.ORCID 0000-0003-1333-0191
S K HowlettDepartment of Clinical Neurosciences, University of Cambridge, Cambridge, UK.ORCID 0000-0003-0504-4937
O SuchanekMolecular Immunity Unit, Department of Medicine, University of Cambridge, Cambridge, UK.
K PolanskiWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.ORCID 0000-0002-2586-9576
H W KingCentre for Immunobiology, Blizard Institute, Queen Mary University of London, London, UK.ORCID 0000-0001-5972-8926
L MamanovaWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.ORCID 0000-0003-1463-8622
N HuangWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.ORCID 0000-0001-8849-038X
P A SzaboDepartment of Microbiology and Immunology, Columbia University Irving Medical Center, New York, NY, USA.ORCID 0000-0003-1603-761X
L RichardsonWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.ORCID 0000-0001-9064-1271
L BoltWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.ORCID 0000-0001-7293-0774
E S FasouliWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.ORCID 0000-0003-1621-3396
K T MahbubaniDepartment of Surgery, University of Cambridge and NIHR Cambridge Biomedical Research Centre, Cambridge, UK.ORCID 0000-0002-1327-2334
M PreteWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.ORCID 0000-0002-5946-821X
L TuckWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.ORCID 0000-0002-1837-7549
N RichozMolecular Immunity Unit, Department of Medicine, University of Cambridge, Cambridge, UK.
Z K TuongWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.ORCID 0000-0002-6735-6808
L CamposWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.ORCID 0000-0003-2445-7120
H S MousaDepartment of Clinical Neurosciences, University of Cambridge, Cambridge, UK.ORCID 0000-0002-8327-7114
E J NeedhamDepartment of Clinical Neurosciences, University of Cambridge, Cambridge, UK.ORCID 0000-0001-7042-7462
S PritchardWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.
T LiWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.ORCID 0000-0002-8240-4476
R ElmentaiteWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.ORCID 0000-0001-7366-5466
J ParkWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.ORCID 0000-0002-1687-2423
E RahmaniCenter for Computational Biology, University of California, Berkeley, Berkeley, CA, USA.
D ChenDepartment of Systems Biology, Columbia University Irving Medical Center, New York, NY, USA.ORCID 0000-0002-9710-1857
D K MenonDepartment of Anaesthesia, University of Cambridge, Cambridge, UK.ORCID 0000-0002-3228-9692
O A BayraktarWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.
L K JamesCentre for Immunobiology, Blizard Institute, Queen Mary University of London, London, UK.ORCID 0000-0002-2252-4636
K B MeyerWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.ORCID 0000-0001-5906-1498
N YosefCenter for Computational Biology, University of California, Berkeley, Berkeley, CA, USA.ORCID 0000-0001-9004-1225
M R ClatworthyWellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.ORCID 0000-0002-3340-9828
P A SimsDepartment of Systems Biology, Columbia University Irving Medical Center, New York, NY, USA.ORCID 0000-0002-3921-4837
D L FarberDepartment of Microbiology and Immunology, Columbia University Irving Medical Center, New York, NY, USA.ORCID 0000-0001-8236-9183
K Saeb-Parsy *Department of Surgery, University of Cambridge and NIHR Cambridge Biomedical Research Centre, Cambridge, UK.ORCID 0000-0002-0633-3696
J L Jones *Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK.ORCID 0000-0003-4974-1371
S A Teichmann *Wellcome Sanger Institute, Wellcome Genome Campus, Hinxton, Cambridge, UK.ORCID 0000-0002-6294-6366
Wellcome Sanger Institute · GBUniversity of Cambridge · GBColumbia University Irving Medical Center · USQueen Mary University of London · GBRagon Institute of MGH, MIT and Harvard · USUniversity of California, Berkeley · USWest Suffolk NHS Foundation Trust · GB

Funding

Transcriptomics and Repertoire ProfilingP01AI106697 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Donna L. Farber · 2013 to 2026
$31.3M
Viral Assays CoreU19AI128949 · NIAID · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Donna L. Farber, Peter Alan Sims · 2017 to 2026
$26.4M
The Organoid and Cell Culture CoreP30DK132710 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Robert F. Schwabe · 2022 to 2026
$7.2M
Immunobiology and alveolar physiology of the aging lungU01HL145547 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI BHATTACHARYA, JAHAR, FARBER, DONNA L. · 2019 to 2022
$2.6M
Impact of CD8+ T cell functionality on HIV viral escapeK22AI066976 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI BETTS, MICHAEL R · 2005 to 2006
$270k
Cancer Research UK 10208European Research Council 646794NHLBI NIH HHS U01 HL145547NIAID NIH HHS K22 AI066976NIAID NIH HHS P01 AI106697NIAID NIH HHS U19 AI128949NIDDK NIH HHS P30 DK132710Wellcome Trust 105924Wellcome Trust 206194
6 · The paper itself

Abstract

Despite their crucial role in health and disease, our knowledge of immune cells within human tissues remains limited. We surveyed the immune compartment of 16 tissues from 12 adult donors by single-cell RNA sequencing and VDJ sequencing generating a dataset of ~360,000 cells. To systematically resolve immune cell heterogeneity across tissues, we developed CellTypist, a machine learning tool for rapid and precise cell type annotation. Using this approach, combined with detailed curation, we determined the tissue distribution of finely phenotyped immune cell types, revealing hitherto unappreciated tissue-specific features and clonal architecture of T and B cells. Our multitissue approach lays the foundation for identifying highly resolved immune cell types by leveraging a common reference dataset, tissue-integrated expression analysis, and antigen receptor sequencing.

Indexed as

B-LymphocytesMachine LearningSequence Analysis, RNASingle-Cell AnalysisT-LymphocytesTranscriptomeCells, CulturedHumansOrgan Specificity

Identifiers

PMID35549406
PMCPMC7612735
OpenAlexW4280596398

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.