Evidence map›Paper›PMID 32298648›Full record

ArticleImmunity2020

Visualization of T Cell Migration in the Spleen Reveals a Network of Perivascular Pathways that Guide Entry into T Zones.

Anne Chauveau, Gabriela Pirgova, Hung-Wei Cheng, Angelina De Martin, Felix Y Zhou, Sarah Wideman, Jens Rittscher, Burkhard Ludewig, Tal I Arnon

Open access · hybridAbstract read
In one paragraph

Article in Immunity, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing papers in PubMed
2.9field-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

37 citing papers in PubMed, 68 citations in OpenAlex.

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  13. Erythroid progenitor cell-mediated spleen-tumor interaction deteriorates cancer immunity.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  14. Review
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  18. Protective fibroblastic niches in secondary lymphoid organs.The Journal of experimental medicine · 2024
    Review
  19. Splenic stromal niches in homeostasis and immunity.Nature reviews. Immunology · 2023
    Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 3 institutions in 2 countries.

Anne ChauveauUniversity of Oxford, Kennedy Institute of Rheumatology, OX3 7FY Oxford, UK.
Gabriela PirgovaUniversity of Oxford, Kennedy Institute of Rheumatology, OX3 7FY Oxford, UK.
Hung-Wei ChengInstitute of Immunobiology, Kantonsspital St. Gallen, 9007 St. Gallen, Switzerland.
Angelina De MartinInstitute of Immunobiology, Kantonsspital St. Gallen, 9007 St. Gallen, Switzerland.
Felix Y ZhouUniversity of Oxford, Ludwig Institute for Cancer Research, OX3 7DQ Oxford, UK.
Sarah WidemanUniversity of Oxford, Kennedy Institute of Rheumatology, OX3 7FY Oxford, UK.
Jens RittscherUniversity of Oxford, Ludwig Institute for Cancer Research, OX3 7DQ Oxford, UK; University of Oxford, Institute of Biomedical Engineering, OX3 7DQ Oxford, UK; University of Oxford, Big Data Institute, Li Ka Shing Centre for Health Information and Discovery, OX3 7XP Oxford, UK.
Burkhard LudewigInstitute of Immunobiology, Kantonsspital St. Gallen, 9007 St. Gallen, Switzerland.
Tal I ArnonUniversity of Oxford, Kennedy Institute of Rheumatology, OX3 7FY Oxford, UK. Electronic address: tal.arnon@kennedy.ox.ac.uk.
University of Oxford · GBKantonsspital St. Gallen · CHLudwig Cancer Research · GB

Funding

Wellcome TrustWellcome Trust 106245/Z/14/Z
6 · The paper itself

Abstract

Lymphocyte homeostasis and immune surveillance require that T and B cells continuously recirculate between secondary lymphoid organs. Here, we used intravital microscopy to define lymphocyte trafficking routes within the spleen, an environment of open blood circulation and shear forces unlike other lymphoid organs. Upon release from arterioles into the red pulp sinuses, T cells latched onto perivascular stromal cells in a manner that was independent of the chemokine receptor CCR7 but sensitive to Gi protein-coupled receptor inhibitors. This latching sheltered T cells from blood flow and enabled unidirectional migration to the bridging channels and then to T zones, entry into which required CCR7. Inflammatory responses modified the chemotactic cues along the perivascular homing paths, leading to rapid block of entry. Our findings reveal a role for vascular structures in lymphocyte recirculation through the spleen, indicating the existence of separate entry and exit routes and that of a checkpoint located at the gate to the T zone.

Indexed as

AnimalsB-LymphocytesCell MovementHumansImmunologic SurveillanceIntravital MicroscopyLuminescent ProteinsLymphocytesMice, Inbred C57BLMice, TransgenicReceptors, CCR7Signal TransductionSpleenT-LymphocytesLuminescent ProteinsReceptors, CCR7bridging channelsGPCRsintravital imaginglymphocyte traffickingspleenT cellsvascular-guided migration

Identifiers

PMID32298648
PMCPMC7237890
OpenAlexW3013408868

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.