Laboratório de Imunofarmacologia, Departamento de Bioquímica e Imunologia, Instituto de Ciências Biológicas (ICB), Universidade Federal de Minas Gerais (UFMG), Av. Antonio Carlos, 6627, Belo Horizonte, Brazil,
Mycopathologia. 2013 Oct;176(3-4):191-9. doi: 10.1007/s11046-013-9679-3. Epub 2013 Jul 23.
Paracoccidioidomycosis is the most important systemic mycosis in South America. In the last decades, it was observed that central nervous system involvement is frequent, occurring in 12.5 % of the cases. The aim of this study was to report the early inflammatory changes associated with an experimental model of neuroparacoccidioidomycosis (NPCM).
C57BL/6 mice were infected by intracranial route with 10(6) yeast cells of PB18 strain of Paracoccidioides brasiliensis. Leukocyte-endothelium interactions were assessed by intravital microscopy 1, 2, 4, and 8 weeks post-infection (p.i.). Chemokine/cytokine levels in the brain and histopathological changes were assessed 4 and 8 weeks p.i..
Intravital microscopy analysis revealed a progressive increase in leukocyte recruitment in the vessels of pia mater with a peak 4 weeks p.i. The chemokine CXCL9 was increased at 4 and 8 weeks p.i., while CCL2, CCL3, and CCL5 were increased at 8 weeks p.i. Histopathological analysis revealed the infiltration of inflammatory cells and the development of progressive granulomatous meningoencephalitis. CCL3 levels correlated with clinical manifestations of disease, as measured by the SHIRPA battery.
The experimental model of NPCM showed increased leukocyte recruitment associated with increased expression of chemokines and nervous tissue inflammation which correlated with clinical manifestations of disease.
球孢子菌病是南美的最重要的系统性真菌病。在过去几十年中,观察到中枢神经系统受累很常见,占病例的 12.5%。本研究的目的是报告与神经球孢子菌病(NPCM)实验模型相关的早期炎症变化。
C57BL/6 小鼠经颅内途径用 10(6)个酵母细胞的巴西副球孢子菌 PB18 株感染。在感染后 1、2、4 和 8 周通过活体显微镜评估白细胞-内皮相互作用。在感染后 4 和 8 周评估脑内趋化因子/细胞因子水平和组织病理学变化。
活体显微镜分析显示,在脑膜血管中的白细胞募集呈渐进性增加,在 4 周时达到峰值。趋化因子 CXCL9 在感染后 4 和 8 周时增加,而 CCL2、CCL3 和 CCL5 在感染后 8 周时增加。组织病理学分析显示炎症细胞浸润和进行性肉芽肿性脑膜脑炎的发展。CCL3 水平与 SHIRPA 电池测量的疾病临床表现相关。
NPCM 的实验模型显示白细胞募集增加,与趋化因子表达增加和神经组织炎症相关,与疾病的临床表现相关。