Avaliação da função macrofágica na hanseníase virchowiana: marcadores de superfície, receptores TLR e NLR e mediadores inflamatórios

• Autor(a) principal: Gigliotti, Patrícia [UNESP]
• Data de Publicação: 2014
• Tipo de documento: Dissertação
• Idioma: por
• Título da fonte: Repositório Institucional da UNESP
• Texto Completo: http://hdl.handle.net/11449/113895
• topic: Hanseniase; Macrofagos; Mycobacterium leprae; Receptores Toll-like; Inflamassomos; Citocinas; Sistema imune

Macrophages play a major role in the elimination of M. leprae (ML). These cells participate in pathogen recognition and activation of the immune system. However in the lepromatous leprosy macrophages become targets, serving as habitat for the bacillus that protects itself from the action of the immune system. This study aimed to evaluate the macrophage function in lepromatous leprosy patients (LLP) in term of surface molecules expression and cytokine and H2O2 production. Moreover, considering the possible involvement of inflammasome complex in macrophage response against ML, inflammasome genes expression was evaluated. ML induced surface expression of activation markers CD40 and ICAM in healthy controls (HC) and LLP macrophages in a similar way, as well as TLRs involved in ML recognition (TLR1 and TLR2). Pro-inflammatory cytokines TNF and IL-1β showed a different behavior. ML was able to induce TNF in HC and LLP, but not IL-1β. Similarly, ML induced significant production of H2O2 in HC but not in LLP macrophages. No difference was found in the production of anti-inflammatory molecules IL-10 and IL1RA in HC and LLP macrophages stimulated with ML. When inflammasome genes expression was analyzed an up-regulation of IL1B gene was observed in both HC and LLP macrophages stimulated with ML. Together, our data indicate that the deficiency in the production of IL-1β and H2O2 in lepromatous leprosy patients combined with IL1B gene expression induction by M. leprae suggested that even if surface recognition of ML and general activation of macrophages are apparently normal, the bacteria is able to inhibits the pathways leading to I IL-1β and H2O2 production, possibly affecting inflammasome activation