El Naggar Heba M, Anwar Mona M, Khayyal Amira E, Abdelhameed Reda M, Barakat Ashraf M, Sadek Sabry A S, Elashkar Ayman M
Department of Medical Parasitology, Faculty of Medicine, Ain Shams University, Cairo, Egypt.
Department of Applied Organic Chemistry, Chemical Industries Research Division, National Research Centre, Giza, Egypt.
J Parasit Dis. 2023 Sep;47(3):591-607. doi: 10.1007/s12639-023-01602-w. Epub 2023 Jun 7.
is an opportunistic intracellular protozoon which may cause severe disease in the immunocompromised patients. Unfortunately, the majority of treatments on the market work against tachyzoites in the acute infection but can't affect tissue cysts in the chronic phase. So, this study aimed to evaluate the effect of bee venom (BV) loaded metal organic frameworks (MOFs) nanoparticles (NPs) for the treatment of chronic murine toxoplasmosis. Ninety laboratory Swiss Albino mice were divided into 9 groups (10 mice each); GI (negative control), GII (infected control), GIII-GXI (infected with Me49 strain of and treated); GIII (MOFs-NPs), GIV and GV (BV alone and loaded on MOFs-NPs), GVI and GVII (spiramycin alone and loaded on MOFs-NPs), GVIII and GIX (ciprofloxacin alone and loaded on MOFs-NPs). Parasitological examination of brain cyst count, histopathological study of brain, retina, liver, and kidney tissue sections and immunohistochemical (IHC) evaluation of liver was performed. Counting of brain cysts showed high statistically significant difference between the infected treated groups and GII. GV showed the least count of brain cysts; mean ± SD (281 ± 29.5). Histopathological examination revealed a marked ameliorative effect of BV administration when used alone or loaded MOFs-NPs. It significantly reduced tissue inflammation, degeneration, and fibrosis. IHC examination of liver sections revealed high density CD8 infiltration in GII, low density CD8 infiltration in GIII, GVI, GVII, GVIII, and GIX while GIV and GV showed intermediate density CD8 infiltration. BV is a promising Apitherapy against chronic toxoplasmosis. This effect is markedly enhanced by MOFs-NPs.
是一种机会性细胞内原生动物,可在免疫功能低下的患者中引起严重疾病。不幸的是,市面上的大多数治疗方法针对急性感染中的速殖子起作用,但对慢性期的组织囊肿无效。因此,本研究旨在评估负载蜂毒(BV)的金属有机框架(MOF)纳米颗粒(NP)对慢性小鼠弓形虫病的治疗效果。90只实验室瑞士白化小鼠分为9组(每组10只);GI(阴性对照),GII(感染对照),GIII - GXI(感染Me49株并接受治疗);GIII(MOF - NP),GIV和GV(单独的BV以及负载在MOF - NP上的BV),GVI和GVII(单独的螺旋霉素以及负载在MOF - NP上的螺旋霉素),GVIII和GIX(单独的环丙沙星以及负载在MOF - NP上的环丙沙星)。进行了脑囊肿计数的寄生虫学检查、脑、视网膜、肝和肾组织切片的组织病理学研究以及肝脏的免疫组织化学(IHC)评估。脑囊肿计数显示,感染治疗组与GII之间存在高度统计学显著差异。GV显示的脑囊肿计数最少;平均值±标准差(281±29.5)。组织病理学检查显示,单独使用BV或负载MOF - NP时,BV给药具有明显的改善作用。它显著减轻了组织炎症、变性和纤维化。肝脏切片的IHC检查显示,GII中CD8浸润密度高,GIII、GVI、GVII、GVIII和GIX中CD8浸润密度低,而GIV和GV显示中等密度的CD8浸润。BV是一种有前途的抗慢性弓形虫病的蜂疗药物。MOF - NP可显著增强这种效果。