Evidence map›Paper›PMID 32010143›Full record

ReviewFrontiers in immunology2019

IL-17A in Psoriasis and Beyond: Cardiovascular and Metabolic Implications.

Esther von Stebut, Wolf-Henning Boehncke, Kamran Ghoreschi, Tommaso Gori, Ziya Kaya, Diamant Thaci, Andreas Schäffler

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 102 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
102citing papers in PubMed, 3 pooled it
9.8field-weighted citation impact, top 1% 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

102 citing papers in PubMed, 3 syntheses or guidelines pooled it, 194 citations in OpenAlex.

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  6. DYRK kinases phosphorylate IL-17RA at S801.Serican journal of medicine · 2026
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42 more citing papers are in PubMed but not listed here.

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 at 7 institutions in 2 countries.

Esther von StebutDepartment of Dermatology, University of Cologne, Cologne, Germany.
Wolf-Henning BoehnckeDivision of Dermatology and Venereology, Geneva University Hospitals, Geneva, Switzerland.
Kamran GhoreschiDepartment of Dermatology, Venereology and Allergology, Charité-Universitätsmedizin Berlin, Berlin, Germany.
Tommaso GoriCenter of Cardiology-Cardiology I, University Medical Center Mainz, Mainz, Germany.
Ziya KayaDepartment of Internal Medicine III, University of Heidelberg, Heidelberg, Germany.
Diamant ThaciInstitute and Comprehensive Center of Inflammation Medicine, University of Lübeck, Lübeck, Germany.
Andreas SchäfflerDepartment of Internal Medicine III, Giessen University Hospital, Giessen, Germany.
Charité - Universitätsmedizin Berlin · DEHeidelberg University · DEJohannes Gutenberg University Mainz · DEUniversitätsklinikum Gießen und Marburg · DEUniversity Hospital of Geneva · CHUniversity of Cologne · DEUniversity of Lübeck · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Interleukin 17A (IL-17A) is one of the currently known six members of the IL-17 cytokine family and is implicated in immune responses to infectious pathogens and in the pathogenesis of inflammatory autoimmune diseases like psoriasis. Psoriatic skin is characterized by high expression of IL-17A and IL-17F, which act on immune and non-immune cell types and strongly contribute to tissue inflammation. In psoriatic lesions, IL-17A, IL-17E, and IL-17F are involved in neutrophil accumulation, followed by the formation of epidermal micro abscesses. IL-17A together with other Th17 cytokines also upregulates the production of several chemokines that are implicated in psoriasis pathogenesis. IL17A-targeting antibodies show an impressive clinical efficacy in patients with psoriasis. Studies have reported an improvement of at least 75% as measured by the psoriasis area and severity index (PASI) in >80% of patients treated with anti-IL-17A therapy. Psoriasis skin manifestations, cardiovascular as well as metabolic disease in psoriasis appear to share pathogenic mechanisms evolving around IL-17A and its proinflammatory role. Thus, anti-IL-17A therapy not only improves skin manifestations of psoriasis, but also cardiovascular inflammation as well as metabolic factors and different domains of psoriatic arthritis (PsA) including peripheral arthritis, enthesitis, dactylitis, and axial involvement. This review summarizes the biological role of IL-17A, before reviewing currently available data on its role in the physiology and pathophysiology of the skin, as well as the cardiovascular and the metabolic system. In conclusion, clinical recommendations for patients with moderate to severe psoriasis based on the current available data are given.

Indexed as

Arthritis, PsoriaticCardiovascular DiseasesHumansInterleukin-17Metabolic DiseasesTh17 CellsIL17A protein, humanIL17F protein, humanIL25 protein, humanInterleukin-17cardiovascularcomorbiditiesdiabetesIL-17Apsoriasis

Identifiers

PMID32010143
PMCPMC6974482
OpenAlexW2999565226

What OpenQuestion holds

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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.