Use este identificador para citar ou linkar para este item: http://higia.imip.org.br/handle/123456789/804
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dc.contributor.authorSilva, Mauro César da-
dc.contributor.authorMedeiros, Fernanda Silva-
dc.contributor.authorSilva, Neila Caroline Henrique da-
dc.contributor.authorPaiva, Larissa Albuquerque-
dc.contributor.authorGomes, Fabiana Oliveira dos Santos-
dc.contributor.authorSilva, Matheus Costa e-
dc.contributor.authorGomes, Thailany Thays-
dc.contributor.authorPeixoto, Christina Alves-
dc.contributor.authorRygaard, Maria Carolina Valença-
dc.contributor.authora Menezes, Maria Luiza Bezerr-
dc.contributor.authorWelkovic, Stefan-
dc.contributor.authorDonadi, Eduardo Antônio-
dc.contributor.authorLucena-Silva, Norma-
dc.date.accessioned2022-07-01T15:25:33Z-
dc.date.available2022-07-01T15:25:33Z-
dc.date.issued2021-
dc.identifier.urihttp://higia.imip.org.br/handle/123456789/804-
dc.description.abstractThe high-risk oncogenic human papillomavirus (HPV) has developed mechanisms for evasion of the immune system, favoring the persistence of the infection. The chronic inflammation further contributes to the progression of tissue injury to cervical cancer. The programmed cell death protein (PD-1) after contacting with its ligands (PD-L1 and PD-L2) exerts an inhibitory effect on the cellular immune response, maintaining the balance between activation, tolerance, and immune cell-dependent lesion. We evaluated 295 patients exhibiting or not HPV infection, stratified according to the location (injured and adjacent non-injured areas) and severity of the lesion (benign, pre-malignant lesions). Additionally, we investigated the role of the promoter region PDCD1 -606G>A polymorphism (rs36084323) on the studied variables. PD-1 and PDCD1 expression were evaluated by immunohistochemistry and qPCR, respectively, and the PDCD1 polymorphism was evaluated by nucleotide sequencing. Irrespective of the severity of the lesion, PD-1 levels were increased compared to adjacent uninjured areas. Additionally, in cervical intraepithelial neoplasia (CIN) I, the presence of HPV was associated with increased (P = 0.0649), whereas in CIN III was associated with decreased (P = 0.0148) PD-1 levels, compared to the uninjured area in absence of HPV infection. The PDCD1 -606A allele was rare in our population (8.7%) and was not associated with the risk for development of HPV infection, cytological and histological features, and aneuploidy. In contrast, irrespective of the severity of the lesion, patients exhibiting the mutant PDCD1 -606A allele at single or double doses exhibited increased protein and gene expression when compared to the PDCD1 -606GG wild type genotype. Besides, the presence of HPV was associated with the decrease in PDCD1 expression and PD-1 levels in carriers of the -606 A allele presenting severe lesions, suggesting that other mediators induced during the HPV infection progression may play an additional role. This study showed that increased PD-1 levels are influenced by the -606G>A nucleotide variation, particularly in low-grade lesions, in which the A allele favors increased PDCD1 expression, contributing to HPV immune system evasion, and in the high-grade lesion, by decreasing tissue PD-1 levels.pt_BR
dc.language.isoenpt_BR
dc.subjectPapillomaviridaept_BR
dc.subjectNeoplasiaspt_BR
dc.subjectReceptor de morte celular programada 1pt_BR
dc.titleIncreased PD-1 level in severe cervical injury is associated with the rare programmed cell death 1 (PDCD1) rs36084323 a allele in a dominant modelpt_BR
dc.higia.programArtigos científicos colaboradores IMIPpt_BR
dc.higia.tipoArtigo Científicopt_BR
dc.higia.pages13 p.pt_BR
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