Universidad de Antioquia, Medellín, Colombia.
Cell Immunol. 2010;266(1):52-60. doi: 10.1016/j.cellimm.2010.08.012. Epub 2010 Sep 21.
Decreased apoptotic cells (ACs) removal has been described as relevant in systemic lupus erythematosus (SLE) pathogenesis. Binding/phagocytosis of ACs was decreased in SLE patients. Blocking experiments suggested a role for CD36 in ACs clearance in healthy controls, not observed in SLE patients. Binding/phagocytosis of ACs induced the production of IL-6, CXCL8 and CCL22 in patients and controls and IL-1β, TNF-α and CCL3 only in healthy controls. ACs clearance induced an increase in CD80 and a decrease in CD86 expression in healthy controls and atherosclerotic patients. However, SLE patients did not up-regulate CD80 expression. The number and expression of CD36 and CD163 in monocytes was not different between the groups. ACs removal induced a down-regulation of CD36 expression in adherent HLA-DR(+) cells in SLE patients but not healthy controls. The decreased binding/phagocytosis of ACs observed in SLE patients, induces a distinct immune response compared with healthy controls.
凋亡细胞 (ACs) 的清除减少已被描述为红斑狼疮 (SLE) 发病机制中的一个重要因素。SLE 患者的 ACs 结合/吞噬作用降低。阻断实验表明 CD36 在健康对照组中对 ACs 清除起作用,但在 SLE 患者中未观察到。ACs 的结合/吞噬作用诱导了患者和对照组中 IL-6、CXCL8 和 CCL22 的产生,而仅在健康对照组中诱导了 IL-1β、TNF-α 和 CCL3 的产生。ACs 清除诱导健康对照组和动脉粥样硬化患者中 CD80 的表达增加和 CD86 的表达减少。然而,SLE 患者并未上调 CD80 的表达。单核细胞中 CD36 和 CD163 的数量和表达在各组之间没有差异。SLE 患者中,ACs 去除诱导黏附 HLA-DR(+) 细胞中 CD36 表达下调,但在健康对照组中未观察到。与健康对照组相比,SLE 患者中观察到的 ACs 结合/吞噬作用降低,诱导了不同的免疫反应。