Costa Inês, Pinto Ana Isabel, Esteves Sofia, Caldas Cátia, Osório Hugo, Santarém Nuno, Fernandez-Becerra Carmen, Cordeiro-da-Silva Anabela
Instituto de Investigação e Inovação em Saúde, Universidade do Porto, 4200-135 Porto, Portugal.
Laboratório de Microbiologia, Departamento de Ciências Biológicas, Faculdade de Farmácia, Universidade do Porto, 4200-135 Porto, Portugal.
Int J Mol Sci. 2025 Jun 13;26(12):5691. doi: 10.3390/ijms26125691.
is an intracellular protozoan parasite that causes leishmaniasis, a disease prevalent in 97 countries. Co-infection with HIV increases susceptibility to visceral leishmaniasis (VL), accelerating HIV's progression to AIDS. Managing VL in HIV-infected individuals is challenging due to atypical presentations and limited therapeutic responses, highlighting the need to develop new disease management strategies. Extracellular vesicles (EVs) hold great promise for this goal as they can be used for a higher understanding of biological processes and biomarker discovery. In this context, a proteomic analysis was carried out from plasma-EVs of an HIV/VL patient over two years and compared to HIV and healthy controls. The analysis confirmed classical EV markers but showed limited detection of proteins. However, variations in human protein abundance related to relevant immunological processes were observed. Notably, the macrophage receptor with a collagenous structure (MARCO) was consistently detected only in the patient and not in the control groups. Significantly, the relevance of MARCO as a possible VL biomarker was confirmed using a validation cohort with five VL patients and its detection by Western Blot was possible. Although MARCO warrants further investigation as a VL related biomarker, the study of EVs confirmed their promise of being a privileged window into this disease. Future studies are needed to broaden data on EVs in infections to improve clinical management.
是一种细胞内原生动物寄生虫,可导致利什曼病,这是一种在97个国家流行的疾病。与艾滋病毒合并感染会增加内脏利什曼病(VL)的易感性,加速艾滋病毒向艾滋病的进展。由于临床表现不典型和治疗反应有限,管理艾滋病毒感染个体中的VL具有挑战性,这凸显了开发新的疾病管理策略的必要性。细胞外囊泡(EVs)有望实现这一目标,因为它们可用于更深入地了解生物过程和发现生物标志物。在此背景下,对一名艾滋病毒/利什曼病患者两年多的血浆细胞外囊泡进行了蛋白质组学分析,并与艾滋病毒感染者和健康对照进行了比较。分析证实了经典的细胞外囊泡标志物,但蛋白质检测有限。然而,观察到与相关免疫过程相关的人类蛋白质丰度存在差异。值得注意的是,仅在患者中持续检测到具有胶原结构的巨噬细胞受体(MARCO),而在对照组中未检测到。重要的是,使用包含五名利什曼病患者的验证队列证实了MARCO作为可能的利什曼病生物标志物的相关性,并且可以通过蛋白质印迹法检测到它。尽管MARCO作为与利什曼病相关的生物标志物值得进一步研究,但对细胞外囊泡 的研究证实了它们有望成为了解这种疾病的特权窗口。需要开展进一步研究以拓宽感染中细胞外囊泡的数据,从而改善临床管理。