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

Priscilla Stela Santana de OliveiraMichelly Cristiny PereiraSimão Kalebe Silva de PaulaEmerson Vasconcelos Andrade LimaMariana Modesto de Andrade LimaRodrigo Gomes de ArrudaWagner Luís Mendes de OliveiraÂngela Luzia Branco Pinto DuarteIvan da Rocha PittaMoacyr Jesus Barreto de Melo RêgoMaira Galdino da Rocha Pitta
Published in: Mediators of inflammation (2016)
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.
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