Evidence map›Paper›PMID 40371466›Full record

ArticleArteriosclerosis, thrombosis, and vascular biology2025

IL-19 Is a Novel Lymphangiocrine Factor Inducing Lymphangiogenesis and Lymphatic Junctional Regulation.

Amanda M Peluzzo, Amanda St Paul, Cali B Corbett, Sheri E Kelemen, Silvia Fossati, Xiaolei Liu, Michael V Autieri

Abstract read
In one paragraph

Article in Arteriosclerosis, thrombosis, and vascular biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Translational cancer research · 2026
    Article
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

7 authors.

Amanda M PeluzzoLemole Center for Integrated Lymphatics and Vascular Research, Lewis Katz School of Medicine at Temple University, Philadelphia, PA (A.M.P., A.S.P., C.B.C., S.E.K., X.L., M.V.A.).
Amanda St PaulLemole Center for Integrated Lymphatics and Vascular Research, Lewis Katz School of Medicine at Temple University, Philadelphia, PA (A.M.P., A.S.P., C.B.C., S.E.K., X.L., M.V.A.).
Cali B CorbettLemole Center for Integrated Lymphatics and Vascular Research, Lewis Katz School of Medicine at Temple University, Philadelphia, PA (A.M.P., A.S.P., C.B.C., S.E.K., X.L., M.V.A.).
Sheri E KelemenLemole Center for Integrated Lymphatics and Vascular Research, Lewis Katz School of Medicine at Temple University, Philadelphia, PA (A.M.P., A.S.P., C.B.C., S.E.K., X.L., M.V.A.).
Silvia FossatiAlzheimer's Center at Temple, Lewis Katz School of Medicine at Temple University, Philadelphia, PA (S.F.).ORCID 0000-0002-2047-222X
Xiaolei LiuLemole Center for Integrated Lymphatics and Vascular Research, Lewis Katz School of Medicine at Temple University, Philadelphia, PA (A.M.P., A.S.P., C.B.C., S.E.K., X.L., M.V.A.).ORCID 0000-0002-6881-3716
Michael V AutieriLemole Center for Integrated Lymphatics and Vascular Research, Lewis Katz School of Medicine at Temple University, Philadelphia, PA (A.M.P., A.S.P., C.B.C., S.E.K., X.L., M.V.A.).ORCID 0000-0003-1039-7577

Funding

Integrative Cardiovascular PathophysiologyT32HL091804 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI ELROD, JOHN WILLIAM · 2008 to 2024
$4.5M
miRNA-mediated reduction of VSMC foam cell formationR01HL117724 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI AUTIERI, MICHAEL V · 2013 to 2022
$3.8M
Targeting carbonic anhydrases in Alzheimer's diseaseR01AG062572 · NIA · TEMPLE UNIV OF THE COMMONWEALTH · PI FOSSATI, SILVIA · 2019 to 2023
$2.3M
Attenuation of atherosclerosis by regulation of VSMC inflammatory gene mRNA stabilityR01HL141108 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI AUTIERI, MICHAEL V · 2018 to 2021
$2.0M
Dissecting the functional roles of cardiac lymphatics in ischemic heart diseaseR01HL163269 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI XIAOLEI LIU · 2023 to 2026
$1.9M
Mechanisms of Th2 interleukin-driven angiogenesisR01HL115575 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI AUTIERI, MICHAEL V · 2013 to 2016
$1.5M
IL-19 Modifies Lymphatic Flux During HyperlipidemiaF30HL172580 · NHLBI · TEMPLE UNIV OF THE COMMONWEALTH · PI Amanda Peluzzo · 2024 to 2026
$125k
NHLBI NIH HHS F30 HL172580NHLBI NIH HHS R01 HL115575NHLBI NIH HHS R01 HL117724NHLBI NIH HHS R01 HL141108NHLBI NIH HHS R01 HL163269NHLBI NIH HHS T32 HL091804NIA NIH HHS R01 AG062572
6 · The paper itself

Abstract

backgroundThe lymphatic system functions by removing fluid, macromolecules, and immune cells to maintain tissue homeostasis. The structural organization of junctional protein complexes is vital to lymphatic function where initial lymphatics have permeable button junctions and collecting lymphatics have relatively impermeable zipper junctions. During inflammation, this junctional morphology appears to reverse, contributing to overall lymphatic malfunction. Little is known about the effects of immunomodulatory cytokines on lymphatic vessel formation and function during inflammation. The purpose of this study is to test the hypothesis that IL (interleukin)-19 promotes lymphangiogenesis and proper lymphatic function during inflammation.

methodsWe used cultured human dermal lymphatic endothelial cells to determine IL-19 expression and its effects on lymphangiogenesis assays. Immunocytochemistry and electric cell-substrate impedance sensing determined effects on junctional morphology as it relates to permeability in vitro. RNA sequencing determined the effects of IL-19 on gene expression.

resultsEndogenous IL-19 expression is induced by exogenous IL-19 and VEGF (vascular endothelial growth factor) C stimulation. IL-19 is lymphangiogenic, increasing human dermal lymphatic endothelial cell migration, network formation, and proliferation. IL-19 induces expression of transcription factors and permeability-associated genes. IL-19 induces rapid VE-cadherin (vascular endothelial cadherin) phosphorylation, increases permeability of human dermal lymphatic endothelial cell monolayers, and mitigates oxidized low-density lipoprotein-associated decrease in human dermal lymphatic endothelial cell permeability. In vivo,

conclusionsTaken together, these data show that IL-19 has potent effects on lymphatic vessel formation and function in vitro and that IL-19 regulates lymphatic drainage in vivo. IL-19 may represent an immunomodulatory cytokine with therapeutic potential for improving impaired lymphatic function consequent to inflammation.

Indexed as

Endothelial CellsIntercellular JunctionsInterleukinsLymphangiogenesisLymphatic VesselsAnimalsAntigens, CDCadherin 5CadherinsCell MovementCells, CulturedHumansMiceMice, Inbred C57BLMice, KnockoutSignal TransductionAntigens, CDCadherin 5CadherinsIL19 protein, humanInterleukinsVascular Endothelial Growth Factor Ccell proliferationhomeostasisinterleukinslipoproteins, LDLlymphatic vessels

Identifiers

PMID40371466
PMCPMC12974107

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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.