人脑实质外神经囊虫病小鼠模型的长期神经影像学表现。

IF 3.8 2区 医学 Q2 CHEMISTRY, MEDICINAL
Alejandro Méndez, Agnes Fleury, Roger Carrillo-Mezo, Juan A. Hernández-Aceves, Montserrat Mejía-Hernández, Nelly Villalobos, Marisela Hernández, Raúl Bobes, Luis Concha, Juan J. Ortiz-Retana, Marta Romano, Pedro Tadao Hamamoto Filho, Gladis Fragoso, José Alejandro Espinosa-Cerón* and Edda Sciutto*, 
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引用次数: 0

摘要

神经囊虫病是由猪带绦虫在中枢神经系统的建立引起的。肺实质外形式(ExP-NCC)是最严重的临床表现,可能多年无症状。目前的治疗包括使用灭囊药物(阿苯达唑和/或吡喹酮)联合糖皮质激素来控制相关的神经炎症;然而,只有约30%的患者有效反应。这突出了改进治疗策略的必要性。本文对人类ExP-NCC实验小鼠模型进行了进一步的表征,以提高其在测试新疗法中的实用性。在人类中,囊肿在蛛网膜下腔的基底池中生长缓慢,患者在感染数年后出现症状。因此,使用磁共振成像(MRI)进行了长期随访,序列允许进行体积分析。MRI证实77%的受感染大鼠有NCC,均表现为肝实质外定位和持续升高的HP10水平,HP10是活囊虫的标志。成像也可以精确定位囊肿和估计寄生虫占据的体积。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Long-Term Neuroimaging Findings in a Murine Model of Human Extraparenchymal Neurocysticercosis

Neurocysticercosis is caused by the establishment of Taenia solium cysticerci in the central nervous system. The extraparenchymal form (ExP-NCC) is the most severe clinical presentation that may remain asymptomatic for years. Current treatment involves cysticidal drugs (albendazole and/or praziquantel) combined with glucocorticoids to manage the associated neuroinflammation; however, only ∼30% of patients respond effectively. This highlights the need to improve therapeutic strategies. Herein, the experimental murine model of human ExP-NCC was further characterized to improve its usefulness in testing new therapies. In humans, cysts grow slowly in the basal cisterns of the subarachnoid space, and patients become symptomatic years after the infection. Thus, a long-term follow-up was performed by using magnetic resonance imaging (MRI) with sequences allowing volumetric analysis. MRI confirmed NCC in 77% of infected rats, all exhibiting extraparenchymal localization and persistently elevated levels of HP10, a marker of viable cysticerci. Imaging also enabled precise cyst localization and estimation of the parasite-occupied volume.

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来源期刊
ACS Infectious Diseases
ACS Infectious Diseases CHEMISTRY, MEDICINALINFECTIOUS DISEASES&nb-INFECTIOUS DISEASES
CiteScore
9.70
自引率
3.80%
发文量
213
期刊介绍: ACS Infectious Diseases will be the first journal to highlight chemistry and its role in this multidisciplinary and collaborative research area. The journal will cover a diverse array of topics including, but not limited to: * Discovery and development of new antimicrobial agents — identified through target- or phenotypic-based approaches as well as compounds that induce synergy with antimicrobials. * Characterization and validation of drug target or pathways — use of single target and genome-wide knockdown and knockouts, biochemical studies, structural biology, new technologies to facilitate characterization and prioritization of potential drug targets. * Mechanism of drug resistance — fundamental research that advances our understanding of resistance; strategies to prevent resistance. * Mechanisms of action — use of genetic, metabolomic, and activity- and affinity-based protein profiling to elucidate the mechanism of action of clinical and experimental antimicrobial agents. * Host-pathogen interactions — tools for studying host-pathogen interactions, cellular biochemistry of hosts and pathogens, and molecular interactions of pathogens with host microbiota. * Small molecule vaccine adjuvants for infectious disease. * Viral and bacterial biochemistry and molecular biology.
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