Evidence map›Paper›PMID 31484769›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

Phenotypically distinct neutrophils patrol uninfected human and mouse lymph nodes.

Laurence S C Lok, Thomas W Dennison, Krishnaa M Mahbubani, Kourosh Saeb-Parsy, Edwin R Chilvers, Menna R Clatworthy

Open access · hybridAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
5.1field-weighted citation impact, top 4% 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

59 citing papers in PubMed, 91 citations in OpenAlex.

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  7. Humanization of CD47 enables development of functional human neutrophils via postirradiation remodeling of the bone marrow.Proceedings of the National Academy of Sciences of the United States of America · 2025
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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

6 authors at 1 institution in 1 country.

Laurence S C LokMolecular Immunity Unit, Department of Medicine, University of Cambridge, Cambridge CB2 0QH, United Kingdom.ORCID 0000-0002-9364-4213
Thomas W DennisonMolecular Immunity Unit, Department of Medicine, University of Cambridge, Cambridge CB2 0QH, United Kingdom.
Krishnaa M MahbubaniDepartment of Surgery, University of Cambridge, Cambridge CB2 0QQ, United Kingdom.
Kourosh Saeb-ParsyDepartment of Surgery, University of Cambridge, Cambridge CB2 0QQ, United Kingdom.
Edwin R ChilversDepartment of Medicine, University of Cambridge, Cambridge CB2 0QQ, United Kingdom; e.chilvers@imperial.ac.uk mrc38@medschl.cam.ac.uk.
Menna R ClatworthyMolecular Immunity Unit, Department of Medicine, University of Cambridge, Cambridge CB2 0QH, United Kingdom; e.chilvers@imperial.ac.uk mrc38@medschl.cam.ac.uk.
University of Cambridge · GB

Funding

Department of Health RP-2017-08-ST2-002Medical Research Council MR/N024907/1Wellcome TrustWellcome Trust 104384/Z/14/Z
6 · The paper itself

Abstract

Neutrophils play a key role in innate immunity. As the dominant circulating phagocyte, they are rapidly recruited from the bloodstream to sites of infection or injury to internalize and destroy microbes. More recently, neutrophils have been identified in uninfected organs, challenging the classical view of their function. Here we show that neutrophils were present in lymph nodes (LNs) in homeostasis. Using flow cytometry and confocal imaging, we identified neutrophils within LNs in naive, unchallenged mice, including LNs draining the skin, lungs, and gastrointestinal tract. Neutrophils were enriched within specific anatomical regions, in the interfollicular zone, a site of T cell activation. Intravital two-photon microscopy demonstrated that LN neutrophils were motile, trafficked into LNs from both blood and tissues via high endothelial venules and afferent lymphatics, respectively, and formed interactions with dendritic cells in LNs. Murine and human LN neutrophils had a distinct phenotype compared with circulating neutrophils, with higher major histocompatibility complex II (MHCII) expression, suggesting a potential role in CD4 T cell activation. Upon ex vivo stimulation with IgG immune complex (IC), neutrophils up-regulated expression of MHCII and costimulatory molecules and increased T cell activation. In vivo, neutrophils were capable of delivering circulating IC to LNs, suggesting a broader functional remit. Overall, our data challenge the perception that neutrophil patrol is limited to the circulation in homeostasis, adding LNs to their routine surveillance territory.

Indexed as

AnimalsCD4-Positive T-LymphocytesCell MovementDendritic CellsFemaleHistocompatibility Antigens Class IIHumansInterferon-gammaLymphatic VesselsLymph NodesLymphocyte ActivationMiceMice, Inbred C57BLNeutrophilsPhenotypeHistocompatibility Antigens Class IIInterferon-gammahomeostasislymph nodeneutrophils

Identifiers

PMID31484769
PMCPMC6754587
OpenAlexW2971859264

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.