Evidence map›Paper›PMID 39640269›Full record

ArticleFrontiers in immunology2024

PTX3 is expressed in terminal lymphatics and shapes their organization and function.

Andrea Doni, Marina Sironi, Annalisa Del Prete, Fabio Pasqualini, Sonia Valentino, Ivan Cuccovillo, Raffaella Parente, Michela Calvi, Antonella Tosoni, Gianluca Vago and 5 more

Abstract read
In one paragraph

Article in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Review
  2. Article
  3. Review
  4. Normal cardiac lymphatics and their mimics.American journal of physiology. Heart and circulatory physiology · 2026
    Article
  5. Review
  6. 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

15 authors.

Andrea Doni *Unit of Multiscale and Nanostructural Imaging, IRCCS Humanitas Research Hospital, Milan, Italy.
Marina Sironi *Cellular and Humoral Innate Immunity Lab, IRCCS Humanitas Research Hospital, Milan, Italy.
Annalisa Del PreteCellular and Humoral Innate Immunity Lab, IRCCS Humanitas Research Hospital, Milan, Italy.
Fabio PasqualiniCellular and Humoral Innate Immunity Lab, IRCCS Humanitas Research Hospital, Milan, Italy.
Sonia ValentinoCellular and Humoral Innate Immunity Lab, IRCCS Humanitas Research Hospital, Milan, Italy.
Ivan CuccovilloCellular and Humoral Innate Immunity Lab, IRCCS Humanitas Research Hospital, Milan, Italy.
Raffaella ParenteUnit of Multiscale and Nanostructural Imaging, IRCCS Humanitas Research Hospital, Milan, Italy.
Michela CalviClinical and Experimental Immunology Lab, IRCCS Humanitas Research Hospital, Milan, Italy.
Antonella TosoniPathology Unit, L. Sacco Hospital, Department of Biomedical and Clinical Sciences, University of Milan, Milan, Italy.
Gianluca VagoPathology Unit, L. Sacco Hospital, Department of Biomedical and Clinical Sciences, University of Milan, Milan, Italy.
Manuela NebuloniPathology Unit, L. Sacco Hospital, Department of Biomedical and Clinical Sciences, University of Milan, Milan, Italy.
Cecilia GarlandaExperimental Immunopathology Lab, IRCCS Humanitas Research Hospital, Milan, Italy.
Annunciata VecchiCellular and Humoral Innate Immunity Lab, IRCCS Humanitas Research Hospital, Milan, Italy.
Barbara BottazziCellular and Humoral Innate Immunity Lab, IRCCS Humanitas Research Hospital, Milan, Italy.
Alberto MantovaniCellular and Humoral Innate Immunity Lab, IRCCS Humanitas Research Hospital, Milan, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The lymphatic system is a multifaceted regulator of tissue homeostasis and an integral part of immune responses. Previous studies had shown that subsets of lymphatic endothelial cells (LEC) express Methods: In the present study using whole-mount imaging and image-based morphometric quantifications, Results: We found that PTX3 is localized in the extracellular matrix (ECM) surrounding human and murine lymphatic vessels (LV). In murine tissues, PTX3 was localized in the ECM close to LV terminals and sprouting. Discussion: Thus, PTX3 is strategically localized in the ECM of specialized LV, playing an essential role in their structural organization and immunological function.

Indexed as

Endothelial CellsLymphatic VesselsMice, KnockoutAnimalsC-Reactive ProteinDendritic CellsExtracellular MatrixHumansMiceMice, Inbred C57BLPentraxinsSerum Amyloid P-ComponentC-Reactive ProteinPentraxinsSerum Amyloid P-Componentextracellular matrixinnate immunitylymphatic systempattern recognition moleculetissue homeostasis

Identifiers

PMID39640269
PMCPMC11617523

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Registered trials

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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.