Innate immune response during DENV-2 infection of monocytes/macrophages

ABSTRACT: The pathogenesis of DENV infection is characterized by a dysregulated inflammatory response and a transient increase in endothelial permeability. Monocytes and macrophages play an essential role during innate immune response against DENV infection, as they are innate sentinels and contribute to viral clearance. Nevertheless, they also contribute to systemic inflammation by producing high levels of soluble factors. This thesis aimed to dissect the role of some innate immune sensors in DENV sensing and induction of inflammatory response of monocytes/macrophages and how this response can be modulated by immunomodulators such as VitD3 and LL-37. By sorting monocyte subsets from PBMCs, we found that TLR2 mediated DENV-2 replication and inflammatory response in classical monocytes, while DENV-2 infection and immune response in non-classical monocytes was mediated by other receptors. Also, TLR2-mediated inflammatory response mediated endothelial dysfunction, underlying the role of classical monocyte in DENV pathogenesis. Vitamin D (VitD3) is known to regulate inflammation and increase antimicrobial peptides expression. Therefore, we evaluated the regulation of innate immune response by VitD3 in monocyte-derived macrophages (MDMs). Differentiation of MDMs in the presence of VitD3 down-regulated the expression of IL-6, TNF-α, RIG-I, TLR3, TLR7, TLR9 and ROS. Furthermore, VitD3 increased the baseline levels of antimicrobial peptide LL-37, which showed antiviral and immunoregulatory functions during in vitro DENV-2 infection of MDMs. Finally, we described that VitD3 can also regulate expression of some miRNAs that have been associated with inflammatory diseases. Overall, our results show two key messages. First, TLR2 has a key role in DENV-2 infection and immune response only in classical monocytes. Secondly, VitD3 and LL-37 have potential as therapeutic candidates as they show both antiviral and immunomodulatory effects against DENV-2 infection in human primary cells.

• Autores: Castillo Ramírez, Jorge Andrés
• Tipo de recurso: Doctoral thesis
• Fecha de publicación: 2022
• Institución: Universidad de Antioquia
• Repositorio: Repositorio UdeA
• Idioma: eng
• OAI Identifier: oai:bibliotecadigital.udea.edu.co:10495/28814
• Acceso en línea: http://hdl.handle.net/10495/28814
• Palabra clave: Virus del dengue; Respuesta inmune; Vitamina D; Macrofagos; Monocitos; Dengue virus; Immunity; Macrophages; Monocytes; Vitamin D; https://id.nlm.nih.gov/mesh/D003716; https://id.nlm.nih.gov/mesh/D007109; https://id.nlm.nih.gov/mesh/D008264; https://id.nlm.nih.gov/mesh/D009000; https://id.nlm.nih.gov/mesh/D014807
• Rights: openAccess
• License: http://purl.org/coar/access_right/c_abf2