系统性硬化症患者单细胞/巨细胞的炎症反应
Tatiana V Kirichenko1,2, Anastasia I Bogatyreva1,3, Elena V Gerasimova3
1Laboratory of Cellular and Molecular Pathology of Cardiovascular System, Petrovsky National Research Center of Surgery, 119435 Moscow, Russia.
Frontiers in bioscience (Landmark edition)
|July 31, 2024
概括
系统性硬化症 (SSc) 患者表现出高度的炎症反应和单细胞/巨细胞的免疫耐受性受损. 单细胞化学吸引蛋白-1 (MCP-1) 的失调可能导致SSc的慢性炎症.
科学领域:
- 免疫学 免疫学 免疫学
- 类风湿病学 类风湿病学
- 细胞生物学 细胞生物学
背景情况:
- 自身免疫性疾病的研究重点是免疫细胞的炎症反应.
- 系统性硬化症 (SSc) 涉及复杂的免疫系统失调.
- 调查SSc中的单细胞/巨细胞炎症状态至关重要.
研究的目的:
- 评估SSc患者单细胞/巨细胞的炎症状态.
- 评估SSc单细胞/巨细胞中的细胞因子分泌概况.
- 为了确定SSc相关炎症的潜在生物标志物.
主要方法:
- 与酶相关的免疫吸收试验 (ELISA) 测量了细胞因子分泌 (TNF-α,IL-1β,MCP-1,IL-8,IL-6).
- 使用了35名SSc患者和25名健康对照组的初级单细胞/巨细胞培养物.
- 脂聚糖 (LPS) 刺激和再刺激评估了免疫反应和耐受性.
主要成果:
- SSc患者的基础和刺激分泌的炎症性细胞因子显著增加.
- 免疫耐受性受损,特别是在单细胞化学吸引蛋白-1 (MCP-1) 分泌中,在31%的SSc患者中观察到.
- 年轻的SSc患者具有较高的抗Scl70抗体水平显示免疫耐受性受损.
结论:
- 在SSc患者中,单细胞/巨细胞表现出促炎激活和免疫耐受性受损.
- MCP-1失调与SSc慢性炎症的发展有关.
- MCP-1代表了SSc治疗的潜在治疗标.
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