Details

Autor(en) / Beteiligte

• da Silva, Mauro César
• Medeiros, Fernanda Silva
• da Silva, Neila Caroline Henrique
• Paiva, Larissa Albuquerque
• Gomes, Fabiana Oliveira Dos Santos
• Costa E Silva, Matheus
• Gomes, Thailany Thays
• Peixoto, Christina Alves
• Rygaard, Maria Carolina Valença
• Menezes, Maria Luiza Bezerra
• Welkovic, Stefan
• Donadi, Eduardo Antônio
• Lucena-Silva, Norma

Titel

Increased PD-1 Level in Severe Cervical Injury Is Associated With the Rare Programmed Cell Death 1 ( PDCD1 ) rs36084323 A Allele in a Dominant Model

Ist Teil von

• Frontiers in cellular and infection microbiology, 2021-07, Vol.11, p.587932-587932

Ort / Verlag

Switzerland: Frontiers Media S.A

Erscheinungsjahr

2021

Quelle

Elektronische Zeitschriftenbibliothek (Open access)

Beschreibungen/Notizen

• The 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 -606G>A polymorphism (rs36084323) on the studied variables. PD-1 and expression were evaluated by immunohistochemistry and qPCR, respectively, and the 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 ( = 0.0649), whereas in CIN III was associated with decreased ( = 0.0148) PD-1 levels, compared to the uninjured area in absence of HPV infection. The -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 -606A allele at single or double doses exhibited increased protein and gene expression when compared to the -606GG wild type genotype. Besides, the presence of HPV was associated with the decrease in 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 expression, contributing to HPV immune system evasion, and in the high-grade lesion, by decreasing tissue PD-1 levels.