4.6 Article

Role of Genetic Polymorphism Present in Macrophage Activation Syndrome Pathway in Post Mortem Biopsies of Patients with COVID-19

Journal

VIRUSES-BASEL
Volume 14, Issue 8, Pages -

Publisher

MDPI
DOI: 10.3390/v14081699

Keywords

SARS-CoV-2; secondary hemophagocytic lymphohistiocytosis; macrophage; immunohistochemistry; polymorphisms

Categories

Funding

  1. CNPq [304356/2018-2]
  2. BRDE-PUCPR (Banco Regional de Desenvolvimento do Extremo Sul)

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This study analyzed lung tissue samples from COVID-19, H1N1, and control groups and found that perforin expression was higher in COVID-19 patients, CD8+ expression was higher in the H1N1 group, and CD57+ expression was higher in the control group. In addition, two genes related to the cytolytic pathway showed associations, and PRF1 rs350947132 was associated with increased immune tissue expression for perforin in the COVID-19 group. The genotype approach can help identify more susceptible patients.
COVID-19 is a viral disease associated with an intense inflammatory response. Macrophage Activation Syndrome (MAS), the complication present in secondary hemophagocytic lymphohistiocytosis (sHLH), shares many clinical aspects observed in COVID-19 patients, and investigating the cytolytic function of the responsible cells for the first line of the immune response is important. Formalin-fixed paraffin-embedded lung tissue samples obtained by post mortem necropsy were accessed for three groups (COVID-19, H1N1, and CONTROL). Polymorphisms in MAS cytolytic pathway (PRF1; STX11; STXBP2; UNC13D and GZMB) were selected and genotyping by TaqMan (R) assays (Thermo Fisher Scientific, MA, USA) using Real-Time PCR (Applied Biosystems, MA USA). Moreover, immunohistochemistry staining was performed with a monoclonal antibody against perforin, CD8+ and CD57+ proteins. Histopathological analysis showed high perforin tissue expression in the COVID-19 group; CD8+ was high in the H1N1 group and CD57+ in the CONTROL group. An association could be observed in two genes related to the cytolytic pathway (PRF1 rs885822 G/A and STXBP2 rs2303115 G/A). Furthermore, PRF1 rs350947132 was associated with increased immune tissue expression for perforin in the COVID-19 group. The genotype approach could help identify patients that are more susceptible, and for this reason, our results showed that perforin and SNPs in the PRF1 gene can be involved in this critical pathway in the context of COVID-19.

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