Department of Immunobiology, University of Lausanne, Epalinges, Switzerland.
Department of Oncology, Ludwig Institute for Cancer Research Lausanne, Lausanne University Hospital and University of Lausanne, Lausanne, Switzerland.
Front Cell Infect Microbiol. 2022 Aug 12;12:941860. doi: 10.3389/fcimb.2022.941860. eCollection 2022.
The lymphatic system plays a crucial role in mounting immune response against intracellular pathogens, and recent studies have documented its role in facilitating tumor dissemination linked largely with cancer cells. However, in mucocutaneous leishmaniasis (MCL) caused by subgenus showing infectious metastasis and resulting in severe distant secondary lesions, the route of escape of these parasites to secondary sites has not yet been investigated in detail. Our results demonstrated that when infection was associated with inflammation and additionally exacerbated by the presence of dsRNA viral endosymbiont (LRV1), lymphatic vessels could serve as efficient routes for infected cells to egress from the primary site and colonize distant organs. We challenged this hypothesis by using the intracellular protozoan parasites associated with or without a dsRNA viral endosymbiont, exacerbating the infection and responsible for a strong inflammatory response, and favoring metastasis of the infection. We analyzed possible cargo cells and the routes of dissemination through flow cytometry, histological analysis, and imaging in our metastatic model to show that parasites disseminated not only intracellularly but also as free extracellular parasites using migrating immune cells, lymph nodes (LNs), and lymph vessels, and followed intricate connections of draining and non-draining lymph node to finally end up in the blood and in distant skin, causing new lesions.
淋巴系统在针对细胞内病原体的免疫反应中起着至关重要的作用,最近的研究记录了其在促进与癌细胞密切相关的肿瘤扩散中的作用。然而,在由亚属引起的粘膜皮肤利什曼病(MCL)中,这些寄生虫逃避到次级部位的途径尚未得到详细研究。我们的研究结果表明,当感染与炎症相关联,并且 dsRNA 病毒内共生体(LRV1)的存在进一步加重时,淋巴管可以成为感染细胞从原发性部位逸出并定植到远处器官的有效途径。我们通过使用与 dsRNA 病毒内共生体相关或不相关的细胞内原生动物寄生虫来挑战这一假设,从而加剧了感染并引发强烈的炎症反应,从而促进了感染的转移。我们通过流式细胞术、组织学分析和转移性模型中的成像分析来分析可能的载体细胞和传播途径,以表明寄生虫不仅在细胞内传播,而且还可以利用迁移免疫细胞、淋巴结(LN)和淋巴管传播,形成游离的外寄生虫,遵循引流和非引流淋巴结的复杂连接,最终进入血液并到达远处皮肤,引发新的病变。