Evidence map›Paper›PMID 33724364›Full record

ArticleThe Journal of experimental medicine2021

ILC3s control splenic cDC homeostasis via lymphotoxin signaling.

Matthias Vanderkerken, Antonio P Baptista, Marco De Giovanni, Satoshi Fukuyama, Robin Browaeys, Charlotte L Scott, Paula S Norris, Gerard Eberl, James P Di Santo, Eric Vivier and 7 more

Open access · greenAbstract read
In one paragraph

Article in The Journal of experimental medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.7field-weighted citation impact, top 35% 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

15 citing papers in PubMed, 19 citations in OpenAlex.

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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

17 authors at 7 institutions in 4 countries.

Matthias Vanderkerken *Laboratory of Immunoregulation and Mucosal Immunology, VIB-UGhent Center for Inflammation Research, Ghent, Belgium.
Antonio P Baptista *Laboratory of Immunoregulation and Mucosal Immunology, VIB-UGhent Center for Inflammation Research, Ghent, Belgium.
Marco De Giovanni *Howard Hughes Medical Institute and Department of Microbiology and Immunology, University of California, San Francisco, San Francisco, CA.
Satoshi FukuyamaDivision of Virology, Department of Microbiology and Immunology, Institute of Medical Science, University of Tokyo, Tokyo, Japan.
Robin BrowaeysData Mining and Modeling for Biomedicine, VIB Center for Inflammation Research, Ghent, Belgium.
Charlotte L ScottLaboratory of Myeloid Cell Ontogeny and Functional Specialization, VIB Center for Inflammation Research, Ghent, Belgium.
Paula S NorrisInfectious and Inflammatory Diseases Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA.
Gerard EberlInstitut Pasteur, Microenvironment and Immunity Unit, Paris, France.
James P Di SantoInstitut Pasteur, Innate Immunity Unit, Department of Immunology, Paris, France.
Eric VivierInnate Pharma Research Laboratories, Innate Pharma, Marseille, France.
Yvan SaeysData Mining and Modeling for Biomedicine, VIB Center for Inflammation Research, Ghent, Belgium.
Hamida HammadLaboratory of Immunoregulation and Mucosal Immunology, VIB-UGhent Center for Inflammation Research, Ghent, Belgium.
Jason G CysterHoward Hughes Medical Institute and Department of Microbiology and Immunology, University of California, San Francisco, San Francisco, CA.
Carl F WareInfectious and Inflammatory Diseases Center, Sanford Burnham Prebys Medical Discovery Institute, La Jolla, CA.
Alexei V Tumanov *Department of Microbiology, Immunology and Molecular Genetics, University of Texas Health Science Center at San Antonio, San Antonio, TX.
Carl De Trez *Laboratory of Cellular and Molecular Immunology, Vrij Universiteit Brussel, Brussels, Belgium.
Bart N Lambrecht *Laboratory of Immunoregulation and Mucosal Immunology, VIB-UGhent Center for Inflammation Research, Ghent, Belgium.
Ghent University Hospital · BEGhent University · BEInserm · FRHoward Hughes Medical Institute · USSanford Burnham Prebys Medical Discovery Institute · USThe University of Texas Health Science Center at San Antonio · USVrije Universiteit Brussel · BE

Funding

Innate lymphoid cells in Campylobacter-induced colitisR21AI135574 · NIAID · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI TUMANOV, ALEXEI V · 2018 to 2019
$419k
European Research Council 789384European Research Council 851908NIAID NIH HHS R21 AI135574
6 · The paper itself

Abstract

The spleen contains a myriad of conventional dendritic cell (cDC) subsets that protect against systemic pathogen dissemination by bridging antigen detection to the induction of adaptive immunity. How cDC subsets differentiate in the splenic environment is poorly understood. Here, we report that LTα1β2-expressing Rorgt+ ILC3s, together with B cells, control the splenic cDC niche size and the terminal differentiation of Sirpα+CD4+Esam+ cDC2s, independently of the microbiota and of bone marrow pre-cDC output. Whereas the size of the splenic cDC niche depended on lymphotoxin signaling only during a restricted time frame, the homeostasis of Sirpα+CD4+Esam+ cDC2s required continuous lymphotoxin input. This latter property made Sirpα+CD4+Esam+ cDC2s uniquely susceptible to pharmacological interventions with LTβR agonists and antagonists and to ILC reconstitution strategies. Together, our findings demonstrate that LTα1β2-expressing Rorgt+ ILC3s drive splenic cDC differentiation and highlight the critical role of ILC3s as perpetual regulators of lymphoid tissue homeostasis.

Indexed as

Immunity, InnateAnimalsCell Adhesion MoleculesDendritic CellsFemaleLymphoid TissueLymphotoxin-alphaLymphotoxin beta ReceptorMiceMice, Inbred C57BLMice, KnockoutMice, TransgenicNuclear Receptor Subfamily 1, Group F, Member 3Receptors, ImmunologicSignal TransductionSpleenCell Adhesion MoleculesEsam protein, mouseLymphotoxin-alphaLymphotoxin beta ReceptorNuclear Receptor Subfamily 1, Group F, Member 3Receptors, ImmunologicSirpa protein, mouse

Identifiers

PMID33724364
PMCPMC7970251
OpenAlexW3136577851

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.