Evidence map›Paper›PMID 28042206›Full record

ArticleMediators of inflammation2016

Increased IL17A, IFNG, and FOXP3 Transcripts in Moderate-Severe Psoriasis: A Major Influence Exerted by IL17A in Disease Severity.

Priscilla Stela Santana de Oliveira, Michelly Cristiny Pereira, Simão Kalebe Silva de Paula, Emerson Vasconcelos Andrade Lima, Mariana Modesto de Andrade Lima, Rodrigo Gomes de Arruda, Wagner Luís Mendes de Oliveira, Ângela Luzia Branco Pinto Duarte, Ivan da Rocha Pitta, Moacyr Jesus Melo Barreto Rêgo and 1 more

Open access · goldAbstract read
In one paragraph

Article in Mediators of inflammation, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 35% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

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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

11 authors at 2 institutions in 1 country.

Priscilla Stela Santana de OliveiraLaboratório de Imunomodulação e Novas Abordagens Terapêuticas (LINAT), Núcleo de Pesquisa em Inovação Terapêutica Suely Galdino (NUPIT-SG), Universidade Federal de Pernambuco (UFPE), Recife, PE, Brazil.
Michelly Cristiny PereiraLaboratório de Imunomodulação e Novas Abordagens Terapêuticas (LINAT), Núcleo de Pesquisa em Inovação Terapêutica Suely Galdino (NUPIT-SG), Universidade Federal de Pernambuco (UFPE), Recife, PE, Brazil.
Simão Kalebe Silva de PaulaLaboratório de Imunomodulação e Novas Abordagens Terapêuticas (LINAT), Núcleo de Pesquisa em Inovação Terapêutica Suely Galdino (NUPIT-SG), Universidade Federal de Pernambuco (UFPE), Recife, PE, Brazil.
Emerson Vasconcelos Andrade LimaHospital das Clínicas, Universidade Federal de Pernambuco (UFPE), Recife, PE, Brazil.
Mariana Modesto de Andrade LimaHospital das Clínicas, Universidade Federal de Pernambuco (UFPE), Recife, PE, Brazil.
Rodrigo Gomes de ArrudaFaculdade Nova Roma, Recife, PE, Brazil.
Wagner Luís Mendes de OliveiraLaboratório de Imunomodulação e Novas Abordagens Terapêuticas (LINAT), Núcleo de Pesquisa em Inovação Terapêutica Suely Galdino (NUPIT-SG), Universidade Federal de Pernambuco (UFPE), Recife, PE, Brazil.ORCID 0000-0001-8555-4093
Ângela Luzia Branco Pinto DuarteHospital das Clínicas, Universidade Federal de Pernambuco (UFPE), Recife, PE, Brazil.
Ivan da Rocha PittaLaboratório de Imunomodulação e Novas Abordagens Terapêuticas (LINAT), Núcleo de Pesquisa em Inovação Terapêutica Suely Galdino (NUPIT-SG), Universidade Federal de Pernambuco (UFPE), Recife, PE, Brazil.
Moacyr Jesus Melo Barreto RêgoLaboratório de Imunomodulação e Novas Abordagens Terapêuticas (LINAT), Núcleo de Pesquisa em Inovação Terapêutica Suely Galdino (NUPIT-SG), Universidade Federal de Pernambuco (UFPE), Recife, PE, Brazil.ORCID 0000-0002-1883-6012
Maira Galdino da Rocha PittaLaboratório de Imunomodulação e Novas Abordagens Terapêuticas (LINAT), Núcleo de Pesquisa em Inovação Terapêutica Suely Galdino (NUPIT-SG), Universidade Federal de Pernambuco (UFPE), Recife, PE, Brazil.ORCID 0000-0001-5881-0338
Universidade Federal de Pernambuco · BRHospital das Clínicas da Universidade Federal de Pernambuco · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Psoriasis is a chronic and recurrent dermatitis, mediated by keratinocytes and T cells. Several proinflammatory cytokines contribute to formation and maintenance of psoriatic plaque. The Th1/Th17 pathways and some of IL-1 family members were involved in psoriasis pathogenesis and could contribute to disease activity. Therefore, we sought to analyse skin transcript levels of IL17A, IL22, RORC, IL8, IFNG, IL33, IL36A, FOXP3, and IL10 and correlate with clinic of patients with plaque-type psoriasis. In order to conduct that, we collected punch biopsies from lesional skin and obtained tissue RNA. After reverse transcription, qRT-PCR quantified the relative mRNA expression. The main results revealed increased transcripts levels of IL17A, IFNG, and FOXP3 in moderate-severe patients. Despite this, only IL17A can increase the chance to worsen disease severity. We also observed many significant positive correlations between each transcript. In conclusion, IL17A is elevated in lesional skin from psoriasis patients and plays crucial role in disease severity.

Indexed as

AdultAgedBrazilCohort StudiesComorbidityCytokinesDermatologyFemaleForkhead Transcription FactorsHumansInterferon-gammaInterleukin-17MaleMiddle AgedPsoriasisSkinCytokinesForkhead Transcription FactorsFOXP3 protein, humanIFNG protein, humanIL17A protein, humanInterferon-gammaInterleukin-17

Identifiers

PMID28042206
PMCPMC5155088
OpenAlexW2557957744

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.