Rosalie Fabian, Eleanor G Bentley, Adam Kirby, Parul Sharma, James P Stewart, Anja Kipar
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These showed that systemic OvHV-2 infection is associated with T cell and macrophage dominated mononuclear infiltrates and vasculitis in various organs. Both T cells and monocytes/macrophages harbor the virus, and infected leukocytes are abundant in the infiltrates. The results also indicate that OvHV-2 has a broader target cell spectrum, including vascular endothelial cells and selected squamous epithelia. The former supports the interpretation that the inflammatory processes develop due to circulating activated, infected T cells and monocytes that home to tissues and emigrate from vessels prone to leukocyte emigration, possibly with direct interaction between virus infected leukocytes and endothelial cells. The latter supports the hypothesis of a graft versus host disease scenario, without viral cytopathic effect on epithelial cells but infiltration of the mucosa by infected T cells and macrophages. 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引用次数: 0
摘要
恶性卡他热(MCF)是一种由γ疱疹病毒引起的反刍动物疾病,通常是致命的,在全球范围内都有影响。绵羊γ疱疹病毒-2(OvHV-2)以绵羊为宿主,是导致易感物种发生恶性卡他热的主要原因。尽管对该疾病的分子方面进行了广泛研究,但对其发病机理尚未完全了解。本研究重新将叙利亚金色仓鼠(Mesocricetus auratus)作为MCF的动物模型,并采用互补的原位方法证实了最近在自然疾病中的发现,从而为MCF的发病机制提供了新的线索。这些研究结果表明,全身性 OvHV-2 感染与 T 细胞和巨噬细胞主导的单核浸润以及各器官的血管炎有关。T 细胞和单核/巨噬细胞都携带病毒,浸润区中有大量受感染的白细胞。研究结果还表明,OvHV-2 的靶细胞谱更广,包括血管内皮细胞和特定的鳞状上皮细胞。前者支持这样的解释,即炎症过程的发生是由于循环中活化的、受感染的 T 细胞和单核细胞进入组织并从容易发生白细胞移出的血管中移出,可能是受病毒感染的白细胞与内皮细胞直接相互作用所致。后者支持移植物对宿主疾病的假设,即病毒对上皮细胞没有细胞病理效应,但受感染的 T 细胞和巨噬细胞会浸润粘膜。在疾病过程中,有证据表明淋巴组织和骨髓中的 T 细胞区和单核细胞/巨噬细胞池扩大。
The golden Syrian hamster (Mesocricetus auratus) as a model to decipher relevant pathogenic aspects of sheep-associated malignant catarrhal fever
Malignant catarrhal fever (MCF) is an often fatal sporadic gammaherpesvirus-induced disease of ruminants with global relevance. Ovine gammaherpesvirus-2 (OvHV-2), with sheep as reservoir host, is a major cause of MCF in susceptible species. Despite extensive research on the molecular aspects of the disease, its pathogenesis is not yet fully understood. The present study re-established the Syrian golden hamster (Mesocricetus auratus) as amenable animal model of MCF and applied complementary in situ approaches to confirm recent findings in natural disease that could shed new light on pathogenetic aspects of MCF. These showed that systemic OvHV-2 infection is associated with T cell and macrophage dominated mononuclear infiltrates and vasculitis in various organs. Both T cells and monocytes/macrophages harbor the virus, and infected leukocytes are abundant in the infiltrates. The results also indicate that OvHV-2 has a broader target cell spectrum, including vascular endothelial cells and selected squamous epithelia. The former supports the interpretation that the inflammatory processes develop due to circulating activated, infected T cells and monocytes that home to tissues and emigrate from vessels prone to leukocyte emigration, possibly with direct interaction between virus infected leukocytes and endothelial cells. The latter supports the hypothesis of a graft versus host disease scenario, without viral cytopathic effect on epithelial cells but infiltration of the mucosa by infected T cells and macrophages. The disease processes are accompanied by evidence of expansion of the T cell compartments and the monocyte/macrophage pool in lymphatic tissues and bone marrow.