Evidence map›Paper›PMID 38177282›Full record

ArticleNature immunology2024

Multimodal profiling reveals site-specific adaptation and tissue residency hallmarks of γδ T cells across organs in mice.

Anastasia du Halgouet, Kerstin Bruder, Nina Peltokangas, Aurélie Darbois, David Obwegs, Marion Salou, Robert Thimme, Maike Hofmann, Olivier Lantz, Sagar

Open access · hybridAbstract read
In one paragraph

Article in Nature immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
8.9field-weighted citation impact, top 2% 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

28 citing papers in PubMed, 37 citations in OpenAlex.

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  16. Ageing, immune fitness and cancer.Nature reviews. Cancer · 2025
    Review
  17. HEB collaborates with TCR signaling to upregulatebioRxiv : the preprint server for biology · 2025
    Article
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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

10 authors at 3 institutions in 3 countries.

Anastasia du HalgouetInstitut National de la Santé et de la Recherche Médicale U932, PSL University, Institut Curie, Paris, France.ORCID http://orcid.org/0000-0001-8013-3716
Kerstin BruderDepartment of Medicine II (Gastroenterology, Hepatology, Endocrinology, and Infectious Diseases), Freiburg University Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Nina PeltokangasMax Planck Institute of Immunobiology and Epigenetics, Freiburg, Germany.
Aurélie DarboisInstitut National de la Santé et de la Recherche Médicale U932, PSL University, Institut Curie, Paris, France.ORCID http://orcid.org/0000-0003-3022-8981
David ObwegsDepartment of Medicine II (Gastroenterology, Hepatology, Endocrinology, and Infectious Diseases), Freiburg University Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
Marion SalouInstitut National de la Santé et de la Recherche Médicale U932, PSL University, Institut Curie, Paris, France.ORCID http://orcid.org/0000-0003-3546-0886
Robert ThimmeDepartment of Medicine II (Gastroenterology, Hepatology, Endocrinology, and Infectious Diseases), Freiburg University Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.ORCID http://orcid.org/0000-0003-1417-4135
Maike HofmannDepartment of Medicine II (Gastroenterology, Hepatology, Endocrinology, and Infectious Diseases), Freiburg University Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany.ORCID http://orcid.org/0000-0001-8410-8833
Olivier LantzInstitut National de la Santé et de la Recherche Médicale U932, PSL University, Institut Curie, Paris, France.ORCID http://orcid.org/0000-0003-3161-7719
SagarDepartment of Medicine II (Gastroenterology, Hepatology, Endocrinology, and Infectious Diseases), Freiburg University Medical Center, Faculty of Medicine, University of Freiburg, Freiburg, Germany. sagar@uniklinik-freiburg.de.ORCID http://orcid.org/0000-0002-8657-4704
University of Freiburg · DEInserm · FRNational Institutes of Health · US

Funding

Agence Nationale de la Recherche (French National Research Agency) ANR-20-CE15-0028-01Deutsche Forschungsgemeinschaft (German Research Foundation) 256073931Deutsche Forschungsgemeinschaft (German Research Foundation) 491676693EC | EU Framework Programme for Research and Innovation H2020 | H2020 Priority Excellent Science | H2020 European Research Council (H2020 Excellent Science - European Research Council) ERC-2019-AdG-885435Fondation pour la Recherche Médicale (Foundation for Medical Research in France) FDT202106013036
6 · The paper itself

Abstract

γδ T cells perform heterogeneous functions in homeostasis and disease across tissues. However, it is unclear whether these roles correspond to distinct γδ subsets or to a homogeneous population of cells exerting context-dependent functions. Here, by cross-organ multimodal single-cell profiling, we reveal that various mouse tissues harbor unique site-adapted γδ subsets. Epidermal and intestinal intraepithelial γδ T cells are transcriptionally homogeneous and exhibit epigenetic hallmarks of functional diversity. Through parabiosis experiments, we uncovered cellular states associated with cytotoxicity, innate-like rapid interferon-γ production and tissue repair functions displaying tissue residency hallmarks. Notably, our observations add nuance to the link between interleukin-17-producing γδ T cells and tissue residency. Moreover, transcriptional programs associated with tissue-resident γδ T cells are analogous to those of CD8

Indexed as

Receptors, Antigen, T-Cell, gamma-deltaT-Lymphocyte SubsetsAnimalsMiceReceptors, Antigen, T-Cell, gamma-delta

Identifiers

PMID38177282
PMCPMC10834366
OpenAlexW4390581929

What OpenQuestion holds

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LicenceCC BY
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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.