Evidence map›Paper›PMID 24655295›Full record

ReviewAnnual review of immunology2014

Immunology of psoriasis.

Michelle A Lowes, Mayte Suárez-Fariñas, James G Krueger

Registry-linked trialOpen access · bronzeAbstract readReview
In one paragraph

Review in Annual review of immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06050330 (CD4+ T Cells and S100A7 Epression in Normal and Psoriatic Skin), which is not on this map. Cited by 804 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
804citing papers in PubMed, 3 pooled it
42.8field-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.

NCT06050330 nacompletednot on this mapstarted 2023, after this paper: background citation

CD4+ T Cells and S100A7 Epression in Normal and Psoriatic Skin: A Histological and Histochemical Study

TypeinterventionalSponsorSohag UniversityRan2023 to 2024Enrolled40ConditionsPsoriasisArmsskin biopsy
3 · Its place in the literature

Who cites it

804 citing papers in PubMed, 3 syntheses or guidelines pooled it, 1,570 citations in OpenAlex.

  1. Pooled it
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  20. Pink lotus flower (Biomedical reports · 2026
    Article

744 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

3 authors at 1 institution in 1 country.

Michelle A LowesLaboratory for Investigative Dermatology, The Rockefeller University, New York, NY 10065; email: lowesm@rockefeller.edu , farinam@rockefeller.edu , jgk@rockefeller.edu.
Mayte Suárez-Fariñas
James G Krueger
Rockefeller University · US

Funding

Transforming Translational Science and Education to Benefit Human HealthUL1TR000043 · NCATS · ROCKEFELLER UNIVERSITY · PI COLLER, BARRY · 2012 to 2015
$26.8M
Origin and Function of Inflammatory Dendritic Cells in Psoriasis.R01AR060222 · NIAMS · ROCKEFELLER UNIVERSITY · PI LOWES, MICHELLE A · 2011 to 2013
$1.1M
NIAMS NIH HHS 1R01AR060222NIAMS NIH HHS R01 AR060222
6 · The paper itself

Abstract

The skin is the front line of defense against insult and injury and contains many epidermal and immune elements that comprise the skin-associated lymphoid tissue (SALT). The reaction of these components to injury allows an effective cutaneous response to restore homeostasis. Psoriasis vulgaris is the best-understood and most accessible human disease that is mediated by T cells and dendritic cells. Inflammatory myeloid dendritic cells release IL-23 and IL-12 to activate IL-17-producing T cells, Th1 cells, and Th22 cells to produce abundant psoriatic cytokines IL-17, IFN-γ, TNF, and IL-22. These cytokines mediate effects on keratinocytes to amplify psoriatic inflammation. Therapeutic studies with anticytokine antibodies have shown the importance of the key cytokines IL-23, TNF, and IL-17 in this process. We discuss the genetic background of psoriasis and its relationship to immune function, specifically genetic mutations, key PSORS loci, single nucleotide polymorphisms, and the skin transcriptome. The association between comorbidities and psoriasis is reviewed by correlating the skin transcriptome and serum proteins. Psoriasis-related cytokine-response pathways are considered in the context of the transcriptome of different mouse models. This approach offers a model for other inflammatory skin and autoimmune diseases.

Indexed as

AnimalsComorbidityDisease Models, AnimalGenetic Predisposition to DiseaseHumansMicePsoriasisSkinSkin Physiological Phenomena

Identifiers

PMID24655295
PMCPMC4229247
OpenAlexW2107432039

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.