Evidence map›Paper›PMID 30415924›Full record

ArticleCell metabolism2019

Interleukin-17 Drives Interstitial Entrapment of Tissue Lipoproteins in Experimental Psoriasis.

Li-Hao Huang, Bernd H Zinselmeyer, Chih-Hao Chang, Brian T Saunders, Andrew Elvington, Osamu Baba, Thomas J Broekelmann, Lina Qi, Joseph S Rueve, Melody A Swartz and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell metabolism, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.5field-weighted citation impact, top 10% 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

35 citing papers in PubMed, 49 citations in OpenAlex.

  1. Review
  2. Article
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  4. Article
  5. Review
  6. Article
  7. A Bibliometric Analysis of Global Research Trends in Psoriasis and Metabolic Syndrome.Clinical, cosmetic and investigational dermatology · 2024
    Article
  8. Review
  9. Article
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  11. Review
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  13. Review
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  18. Article
  19. Article
  20. Psoriasis: Comorbidities.The Journal of dermatology · 2021
    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

16 authors at 4 institutions in 2 countries.

Li-Hao HuangDepartment of Pathology & Immunology, Washington University, St Louis, MO 63110, USA.
Bernd H ZinselmeyerDepartment of Pathology & Immunology, Washington University, St Louis, MO 63110, USA.
Chih-Hao ChangDepartment of Pathology & Immunology, Washington University, St Louis, MO 63110, USA.
Brian T SaundersDepartment of Pathology & Immunology, Washington University, St Louis, MO 63110, USA.
Andrew ElvingtonDepartment of Pathology & Immunology, Washington University, St Louis, MO 63110, USA.
Osamu BabaDepartment of Pathology & Immunology, Washington University, St Louis, MO 63110, USA.
Thomas J BroekelmannDepartment of Cell Biology, Washington University, St Louis, MO 63110, USA.
Lina QiDepartment of Pathology & Immunology, Washington University, St Louis, MO 63110, USA.
Joseph S RueveDepartment of Pathology & Immunology, Washington University, St Louis, MO 63110, USA.
Melody A SwartzDivision of Dermatology, Department of Medicine, Washington University, St Louis, MO 63110, USA.
Brian S KimInstitute for Molecular Engineering, University of Chicago, Chicago, IL 60637, USA.
Robert P MechamDepartment of Cell Biology, Washington University, St Louis, MO 63110, USA.
Helge WiigDepartment of Biomedicine, University of Bergen, Jonas Lies vei 91, Bergen 5009, Norway.
Michael J ThomasDepartment of Pharmacology and Toxicology, Medical College of Wisconsin, Milwaukee, WI 53226, USA.
Mary G Sorci-ThomasDepartment of Medicine, Division of Endocrinology, Pharmacology and Toxicology, and Blood Research Institute, Medical College of Wisconsin, Milwaukee, WI 53226, USA.
Gwendalyn J RandolphDepartment of Pathology & Immunology, Washington University, St Louis, MO 63110, USA. Electronic address: gjrandolph@wustl.edu.
Washington University in St. Louis · USMedical College of Wisconsin · USUniversity of Bergen · NOUniversity of Chicago · US

Funding

Washington University Nutrition Obesity Research CenterP30DK056341 · NIDDK · WASHINGTON UNIVERSITY · PI Dominic N Reeds · 1999 to 2026
$30.2M
TRAINING PROGRAM IN IMMUNOLOGY AND IMMUNOGENETICST32AI007163 · NIAID · WASHINGTON UNIVERSITY · PI Kenneth M Murphy, Kodi S Ravichandran · 1985 to 2026
$14.8M
PRINCIPLES IN CARDIVASCULAR RESEARCH TRAINING PROGRAMT32HL007081 · NHLBI · WASHINGTON UNIVERSITY · PI Abhinav Diwan, Karen Ellen Joynt Maddox · 1985 to 2026
$10.6M
DIFFERENTIATION AND FUNCTION OF MONOCYTES AND MACROPHAGESR37AI049653 · NIAID · WASHINGTON UNIVERSITY · PI RANDOLPH, GWENDALYN J · 2016 to 2025
$4.3M
INTEGRATING CELL & LIPOPROTEIN TRAFFICKING WITH VASCULAR BIOLOGY IN HUMAN IBDDP1DK109668 · NIDDK · WASHINGTON UNIVERSITY · PI RANDOLPH, GWENDALYN J · 2015 to 2019
$3.8M
T Regulatory Lymphocytes, HDL Function, and AtherosclerosisR01HL112276 · NHLBI · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI HEDRICK, CATHERINE C, SORCI-THOMAS, MARY G · 2013 to 2016
$2.8M
Biogenesis of HDL Through Cholesterol Efflux and ApoA-I Structural ReorganizationR01HL127649 · NHLBI · MEDICAL COLLEGE OF WISCONSIN · PI SORCI-THOMAS, MARY G · 2015 to 2018
$2.2M
VEGF-C/VEGFR3 AND LYMPHATIC TRANSPORT OF CHOLESTEROL FROM ATHEROSCLEROTIC PLAQUER01HL118206 · NHLBI · WASHINGTON UNIVERSITY · PI RANDOLPH, GWENDALYN J · 2014 to 2017
$1.5M
NHLBI NIH HHS R01 HL112276NHLBI NIH HHS R01 HL118206NHLBI NIH HHS R01 HL127649NHLBI NIH HHS T32 HL007081NIAID NIH HHS R37 AI049653NIAID NIH HHS T32 AI007163NIDDK NIH HHS DP1 DK109668NIDDK NIH HHS P30 DK056341
6 · The paper itself

Abstract

Lipoproteins trapped in arteries drive atherosclerosis. Extravascular low-density lipoprotein undergoes receptor uptake, whereas high-density lipoprotein (HDL) interacts with cells to acquire cholesterol and then recirculates to plasma. We developed photoactivatable apoA-I to understand how HDL passage through tissue is regulated. We focused on skin and arteries of healthy mice versus those with psoriasis, which carries cardiovascular risk in man. Our findings suggest that psoriasis-affected skin lesions program interleukin-17-producing T cells in draining lymph nodes to home to distal skin and later to arteries. There, these cells mediate thickening of the collagenous matrix, such that larger molecules including lipoproteins become entrapped. HDL transit was rescued by depleting CD4

Indexed as

AnimalsApolipoprotein A-IAtherosclerosisBiological TransportCD4-Positive T-LymphocytesDisease Models, AnimalHEK293 CellsHumansInterleukin-17Lipoproteins, HDLMiceMice, Inbred C57BLMice, KnockoutProtein-Lysine 6-OxidasePsoriasisSkinApolipoprotein A-IInterleukin-17Lipoproteins, HDLProtein-Lysine 6-Oxidasearteryatherosclerosisautoimmunitycollagencytokinesextracellular matrixfibrosisinterstitial transportskinTh17 immunity

Identifiers

PMID30415924
PMCPMC6365189
OpenAlexW2900284252

What OpenQuestion holds

Textmetadata
LicenceTDM
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.