Evidence map›Paper›PMID 36991561›Full record

ArticleEuropean journal of immunology2023

Fibroblastic reticular cells provide a supportive niche for lymph node-resident macrophages.

Joshua D'Rozario, Konstantin Knoblich, Mechthild Lütge, Christian Pérez Shibayama, Hung-Wei Cheng, Yannick O Alexandre, David Roberts, Joana Campos, Emma E Dutton, Muath Suliman and 7 more

Open access · hybridAbstract read
In one paragraph

Article in European journal of immunology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

16 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. CXCR4 coordinates adhesion, migration, and development of human NK cells.bioRxiv : the preprint server for biology · 2026
    Article
  4. Article
  5. Article
  6. Article
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  8. Review
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  10. Article
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  12. Review
  13. Protective fibroblastic niches in secondary lymphoid organs.The Journal of experimental medicine · 2024
    Review
  14. Review
  15. Article
  16. Review
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 9 institutions in 6 countries.

Joshua D'RozarioDepartment of Biochemistry and Molecular Biology, and Monash Biomedicine Discovery Institute, Monash University, Clayton, Australia.
Konstantin KnoblichDepartment of Biochemistry and Molecular Biology, and Monash Biomedicine Discovery Institute, Monash University, Clayton, Australia.
Mechthild LütgeInstitute of Immunobiology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Christian Pérez ShibayamaInstitute of Immunobiology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Hung-Wei ChengInstitute of Immunobiology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Yannick O AlexandreDepartment of Microbiology and Immunology, The Peter Doherty Institute for Infection and Immunity, The University of Melbourne, VIC, Melbourne, Australia.
David RobertsInstitute of Immunology and Immunotherapy, University of Birmingham, Birmingham, UK.
Joana CamposInstitute of Inflammation and Ageing, University of Birmingham, Birmingham, UK.
Emma E DuttonInstitute of Immunology and Immunotherapy, University of Birmingham, Birmingham, UK.
Muath SulimanInstitute of Immunology and Immunotherapy, University of Birmingham, Birmingham, UK.
Alice E DentonDepartment of Immunology and Inflammation, Imperial College London, London, UK.
Shannon J TurleyDepartment of Cancer Immunology, Genentech Inc., South San Francisco, CA, USA.
Richard L BoydCartherics Pty Ltd, Hudson Institute for Medical Research, Clayton, Australia.
Scott N MuellerDepartment of Microbiology and Immunology, The Peter Doherty Institute for Infection and Immunity, The University of Melbourne, VIC, Melbourne, Australia.ORCID 0000-0002-3838-3989
Burkhard LudewigInstitute of Immunobiology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Tracy S P Heng *Department of Anatomy and Developmental Biology, Monash Biomedicine Discovery Institute, Monash University, Clayton, Australia.
Anne L Fletcher *Department of Biochemistry and Molecular Biology, and Monash Biomedicine Discovery Institute, Monash University, Clayton, Australia.ORCID 0000-0003-1534-1142
Kantonsspital St. Gallen · CHDiscovery Institute · USNIHR Birmingham Biomedical Research Centre · GBThe University of Melbourne · AUCancer Research Institute · USHudson Institute of Medical Research · AUImperial College London · GBUniversity of Birmingham · GBUniversity of Cologne · DE

Funding

Wellcome TrustWellcome Trust 109783/Z/15/Z
6 · The paper itself

Abstract

The lymph node (LN) is home to resident macrophage populations that are essential for immune function and homeostasis, but key factors controlling this niche are undefined. Here, we show that fibroblastic reticular cells (FRCs) are an essential component of the LN macrophage niche. Genetic ablation of FRCs caused rapid loss of macrophages and monocytes from LNs across two in vivo models. Macrophages co-localized with FRCs in human LNs, and murine single-cell RNA-sequencing revealed that FRC subsets broadly expressed master macrophage regulator CSF1. Functional assays containing purified FRCs and monocytes showed that CSF1R signaling was sufficient to support macrophage development. These effects were conserved between mouse and human systems. These data indicate an important role for FRCs in maintaining the LN parenchymal macrophage niche.

Indexed as

FibroblastsSignal TransductionAnimalsHumansLymph NodesMacrophagesMiceCSF1Fibroblastic reticular cellsHuman lymph nodesLymph node stromal cellsMacrophages

Identifiers

PMID36991561
PMCPMC10947543
OpenAlexW4361277495

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.