人类真菌感染的细胞外囊泡:免疫反应的关键参与者

Caroline P. de Rezende, Patrick W. S. Santos, Renan A. Piraine, Virgínia C. Silvestrini, Julio C. J. Barbosa, Fabiana C. P. Valera, Edwin Tamashiro, Guilherme G. Podolski-Gondim, Silvana M. Quintana, Rodrigo Calado, Roberto Martinez, Taicia P. Fill, Márcio L. Rodrigues, Fausto Almeida
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引用次数: 0

摘要

真菌感染每年造成约160万人死亡。诊断和治疗真菌感染是困难的,因为获得诊断测试的机会有限,抗真菌药物耐药性上升。细胞外囊泡(EVs)促进真菌细胞与宿主之间的相互作用,显著影响病原体与宿主的关系。由于真菌EVs的复杂性和缺乏对其在人类感染中的作用的临床研究,我们分析了白色念珠菌、新型隐球菌和巴西副球虫感染患者的血清和尿液样本中的EVs,以确定它们的作用。通过质谱分析,我们鉴定出甾醇、鞘脂和脂肪酸是ev中的关键代谢物。我们量化了胆固醇和麦角甾醇,证实在临床样本中存在宿主和真菌EVs。我们的研究探讨了这些ev是否可以调节宿主的免疫反应。我们在小鼠和人巨噬细胞中观察到促炎反应,其特征是细胞因子增加,如肿瘤坏死因子-α、干扰素-γ和白细胞介素-6,以及诱导型一氧化氮合酶基因(M1巨噬细胞反应的标志)的表达升高。因此,真菌感染患者循环EVs可能在疾病病理生理中发挥作用。这些发现增强了我们对真菌感染中EVs的理解,提示了系统性真菌病的潜在治疗靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Extracellular Vesicles From Fungal Infection in Humans: A Key Player in Immunological Responses

Extracellular Vesicles From Fungal Infection in Humans: A Key Player in Immunological Responses

Extracellular Vesicles From Fungal Infection in Humans: A Key Player in Immunological Responses

Extracellular Vesicles From Fungal Infection in Humans: A Key Player in Immunological Responses

Fungal infections cause approximately 1.6 million deaths annually. Diagnosing and treating fungal infections is difficult due to limited access to diagnostic tests and rising antifungal resistance. Extracellular vesicles (EVs) facilitate interactions between fungal cells and hosts, significantly influencing the pathogen-host relationship. Owing to the complexity of fungal EVs and the lack of clinical studies on their roles in human infections, we analysed EVs from serum and urine samples of patients with infections caused by Candida albicans, Cryptococcus neoformans, and Paracoccidioides brasiliensis to determine their roles. Using mass spectrometry, we identified sterols, sphingolipids, and fatty acids as key metabolites in the EVs. We quantified cholesterol and ergosterol, confirming the presence of both host and fungal EVs in clinical samples. Our research investigated whether these EVs could modulate the host immune response. We observed a proinflammatory response in murine and human macrophages, characterized by increased cytokines, such as tumour necrosis factor-α, interferon-γ, and interleukin-6, and elevated expression of the inducible nitric oxide synthase gene, a marker of M1 macrophage response. Thus, circulating EVs in patients with fungal infections likely play a role in disease pathophysiology. These findings enhance our understanding of EVs in fungal infections, suggesting potential therapeutic targets for systemic mycoses.

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