Gonçalves Amanda Costa, Maia Danielle Cardoso Geraldo, Ferreira Lucas Souza, Monnazzi Luis Gustavo Silva, Alegranci Pâmela, Placeres Marisa Campos Polesi, Batista-Duharte Alexander, Carlos Iracilda Zeppone
Department of Clinical Analyses, Faculty of Pharmaceutical Sciences, São Paulo State University, Rua Expedicionários do Brasil, 1621, Araraquara, São Paulo, 14801-902, Brazil.
Mycopathologia. 2015 Feb;179(1-2):21-30. doi: 10.1007/s11046-014-9810-0. Epub 2014 Sep 10.
Sporotrichosis is a chronic infection caused by the dimorphic fungus Sporothrix schenckii, involving all layers of skin and the subcutaneous tissue. The role of innate immune toll-like receptors 2 and 4 in the defense against this fungus has been reported, but so far, there were no studies on the effect of cell wall major components over the cytosolic oligo-merization domain (NOD)-like receptors, important regulators of inflammation and responsible for the maturation of IL-1β and IL-18, whose functions are dependents of the caspase-1 activation, that can participate of inflammasome. It was evaluated the percentage of activation of caspase-1, the production of IL-1β, IL-18, IL-17, IFN-γ and nitric oxide in a Balb/c model of S. schenckii infection. It was observed a decreased activity of caspase-1 during the fourth and sixth weeks of infection accompanied by reduced secretion of the cytokines IL-1β, IL-18 and IL-17 and high production of nitric oxide. IFN-γ levels were elevated during the entire time course of infection. This temporal reduction in caspase-1 activity coincides exactly with the reported period of fungal burden associated with a transitory immunosuppression induced by this fungus and detected in similar infection models. These results indicate the importance of interaction between caspase-1, cytokines IL-1β and IL-18 in the host defense against S. schenckii infection, suggesting a participation the inflammasome in this response.
孢子丝菌病是由双相真菌申克孢子丝菌引起的一种慢性感染,累及皮肤全层和皮下组织。已有报道称天然免疫Toll样受体2和4在抵御这种真菌中发挥作用,但迄今为止,尚未有关于细胞壁主要成分对胞质寡聚化结构域(NOD)样受体影响的研究,NOD样受体是炎症的重要调节因子,负责白细胞介素-1β(IL-1β)和白细胞介素-18(IL-18)的成熟,其功能依赖于半胱天冬酶-1的激活,而半胱天冬酶-1可参与炎性小体的形成。本研究评估了在申克孢子丝菌感染的Balb/c模型中半胱天冬酶-1的激活百分比、IL-1β、IL-18、IL-17、干扰素-γ(IFN-γ)和一氧化氮的产生情况。结果发现,在感染的第四周和第六周,半胱天冬酶-1的活性降低,同时伴有细胞因子IL-1β、IL-18和IL-17分泌减少以及一氧化氮的高产量。在整个感染过程中,IFN-γ水平均升高。半胱天冬酶-1活性的这种暂时降低与报道的真菌负荷期完全一致,该时期与这种真菌诱导的短暂免疫抑制相关,并且在类似的感染模型中也能检测到。这些结果表明半胱天冬酶-1、细胞因子IL-1β和IL-18之间的相互作用在宿主抵御申克孢子丝菌感染中具有重要作用,提示炎性小体参与了这一反应。