Evidence map›Paper›PMID 29641699›Full record

ArticleAnais brasileiros de dermatologia

The potential role of Th17 lymphocytes in patients with psoriasis.

Mahnaz Mansouri, Parvine Mansouri, Abbas Ali Raze, Zohreh Jadali

Open access · goldAbstract read
In one paragraph

Article in Anais brasileiros de dermatologia. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.3field-weighted citation impact, top 22% 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

8 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Circulating CD14Evidence-based complementary and alternative medicine : eCAM · 2020
    Article
  8. Advances in Understanding the Immunological Pathways in Psoriasis.International journal of molecular sciences · 2019
    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

4 authors at 2 institutions in 1 country.

Mahnaz MansouriDepartment of Molecular Medicine, Pasteur Institute of Iran, Tehran, Iran.
Parvine MansouriDepartment of Dermatology and Laser Surgery, Skin and Stem cell Research Center, Tehran University of Medical Sciences, Tehran, Iran.
Abbas Ali RazeDepartment of Medical Biotechnology, Biotechnology Research Center (BRC), Pasteur Institute of Iran, Tehran, Iran.
Zohreh JadaliDepartment of Immunology, School of Public Health, Tehran University of Medical Sciences. Tehran, Iran.
Pasteur Institute of Iran · IRTehran University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPsoriasis is a chronic inflammatory disorder, characterized by increased keratinocyte proliferation due to abnormal differentiation of basal keratinocytes. The etiology of the disease is unclear, and according to the survey results, it is hypothesized that a combination of genetic and environmental factors prompts an abnormal immune response in patients with psoriasis. CD4+ Th cells play a multifaceted role in both immune defense and pathogenesis of certain diseases such as psoriasis. Nonetheless, the exact contribution of different subpopulations of Th cells in psoriasis is still not clear.

objectiveThe aim of present study was to determine the mRNA expression level of RORC as potential inducer of Th17 cell differentiation and expression pattern of Th17-signature cytokines (IL-17A and IL-22).

methodsTwenty patients with psoriasis and twenty-one healthy subjects were included in the study. Peripheral blood mononuclear cells (PBMCs) were separated and expression of three genes were determined by quantitative real-time reverse transcriptase PCR (qRT-PCR). Plasma levels of IL-17 and IL-22 were also evaluated by ELISA.

resultsRORC, IL-17A and IL-22 gene expression was significantly higher in patients with psoriasis compared with healthy controls (P<0.05). In addition, a marked increase in plasma IL-17A and IL-22 levels was observed in patient group compared to controls (P<0.001). STUDY LIMITATIONS: small number of patients.

conclusionThese data suggest that Th17 response may contribute to the pathogenesis of psoriasis.

Indexed as

AdolescentAdultAgedCase-Control StudiesCell DifferentiationFemaleGene ExpressionHumansInterleukin-17Interleukin-22InterleukinsKeratinocytesMaleMiddle AgedNuclear Receptor Subfamily 1, Group F, Member 3PsoriasisIL17A protein, humanInterleukin-17Interleukin-22InterleukinsNuclear Receptor Subfamily 1, Group F, Member 3RNA, MessengerRORC protein, human

Identifiers

PMID29641699
PMCPMC5871364
OpenAlexW2795667019

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.