Evidence map›Paper›PMID 27415420›Full record

ArticlePLoS biology2016

Topological Small-World Organization of the Fibroblastic Reticular Cell Network Determines Lymph Node Functionality.

Mario Novkovic, Lucas Onder, Jovana Cupovic, Jun Abe, David Bomze, Viviana Cremasco, Elke Scandella, Jens V Stein, Gennady Bocharov, Shannon J Turley and 1 more

Open access · goldAbstract read
In one paragraph

Article in PLoS biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed, 2 pooled it
8.2field-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

63 citing papers in PubMed, 2 syntheses or guidelines pooled it, 121 citations in OpenAlex.

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  16. Protective fibroblastic niches in secondary lymphoid organs.The Journal of experimental medicine · 2024
    Review
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  19. PI16Nature immunology · 2023
    Article
  20. Article

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

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

11 authors at 4 institutions in 3 countries.

Mario NovkovicInstitute of Immunobiology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Lucas OnderInstitute of Immunobiology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Jovana CupovicInstitute of Immunobiology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Jun AbeTheodor Kocher Institute, University of Bern, Bern, Switzerland.
David BomzeInstitute of Immunobiology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Viviana CremascoNovartis Institutes for Biomedical Research, Cambridge, Massachusetts, United States of America.
Elke ScandellaInstitute of Immunobiology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Jens V SteinTheodor Kocher Institute, University of Bern, Bern, Switzerland.
Gennady BocharovInstitute of Numerical Mathematics, Russian Academy of Sciences, Moscow, Russia.ORCID 0000-0002-5049-0656
Shannon J TurleyDepartment of Cancer Immunology, Genentech, South San Francisco, California, United States of America.
Burkhard LudewigInstitute of Immunobiology, Kantonsspital St. Gallen, St. Gallen, Switzerland.
Kantonsspital St. Gallen · CHUniversity of Bern · CHNovartis (United States) · USRussian Academy of Sciences · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fibroblastic reticular cells (FRCs) form the cellular scaffold of lymph nodes (LNs) and establish distinct microenvironmental niches to provide key molecules that drive innate and adaptive immune responses and control immune regulatory processes. Here, we have used a graph theory-based systems biology approach to determine topological properties and robustness of the LN FRC network in mice. We found that the FRC network exhibits an imprinted small-world topology that is fully regenerated within 4 wk after complete FRC ablation. Moreover, in silico perturbation analysis and in vivo validation revealed that LNs can tolerate a loss of approximately 50% of their FRCs without substantial impairment of immune cell recruitment, intranodal T cell migration, and dendritic cell-mediated activation of antiviral CD8+ T cells. Overall, our study reveals the high topological robustness of the FRC network and the critical role of the network integrity for the activation of adaptive immune responses.

Indexed as

AnimalsCD8-Positive T-LymphocytesCell CommunicationCell CountCell MovementChemokine CCL19Dendritic CellsFibroblastsLymph NodesMice, Inbred C57BLMice, TransgenicMicroscopy, ConfocalModels, ImmunologicalReceptors, Antigen, T-Cell, alpha-betaT-LymphocytesChemokine CCL19Receptors, Antigen, T-Cell, alpha-beta

Identifiers

PMID27415420
PMCPMC4945005
OpenAlexW2470185571

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.