继发性登革病毒感染中血小板凋亡和巨噬细胞对凋亡血小板的清除。
Platelet apoptosis and apoptotic platelet clearance by macrophages in secondary dengue virus infections.
机构信息
Laboratory for Clinical Research on Infectious Diseases, International Research Center for Infectious Diseases, Osaka University, Japan.
出版信息
J Infect Dis. 2012 Apr 15;205(8):1321-9. doi: 10.1093/infdis/jis180. Epub 2012 Mar 1.
BACKGROUND
The mechanisms of thrombocytopenia and platelet phagocytosis in dengue illness are not fully understood.
METHODS
A prospective hospital-based study was conducted to examine the relationships between platelet counts, serum thrombopoietin (TPO) levels, and platelet apoptosis and phagocytosis in 81 patients with secondary dengue virus (DV) infections and 38 healthy volunteers. The apoptosis and phagocytosis of cultured platelets after exposure to DV were also examined.
RESULTS
Platelet apoptosis, platelet phagocytosis, and serum TPO levels were increased significantly in patients during the acute and early convalescence phases compared with levels observed in patients during the convalescence phase and in healthy volunteers. A significant correlation between platelet apoptosis and platelet phagocytosis was also observed in these patients. Platelet phagocytosis was inhibited significantly by the D89E mutant, which carries a point mutation in the RGD motif of milk fat globule-epidermal growth factor 8, a phosphatidylserine-recognizing bridge molecule. DV-induced platelet apoptosis and increased phagocytosis of DV-induced apoptotic platelets was confirmed using in vitro assays.
CONCLUSIONS
Our data suggest an increased phagocytosis of DV-induced apoptotic platelets by macrophages via a phosphatidylserine-recognizing pathway in secondary DV infection. Accelerated platelet clearance, however, was overcome by TPO-induced enhanced thrombopoiesis in these patients.
CLINICAL TRIALS REGISTRATION
UMIN000004835.
背景
登革热疾病中血小板减少和血小板吞噬的机制尚未完全阐明。
方法
进行了一项前瞻性的基于医院的研究,以检查 81 例继发登革病毒(DV)感染患者和 38 名健康志愿者的血小板计数、血清血小板生成素(TPO)水平与血小板凋亡和吞噬之间的关系。还检查了暴露于 DV 后培养血小板的凋亡和吞噬作用。
结果
与恢复期患者和健康志愿者相比,急性和早期恢复期患者的血小板凋亡、血小板吞噬和血清 TPO 水平显著增加。这些患者中还观察到血小板凋亡与血小板吞噬之间存在显著相关性。载有乳脂肪球表皮生长因子 8 的 RGD 基序中一个点突变的 D89E 突变体显著抑制了血小板吞噬作用,乳脂肪球表皮生长因子 8 是一种识别血小板磷脂酰丝氨酸的桥分子。通过体外实验证实了 DV 诱导的血小板凋亡和对 DV 诱导的凋亡血小板吞噬作用的增加。
结论
我们的数据表明,在继发的 DV 感染中,巨噬细胞通过识别磷脂酰丝氨酸的途径吞噬 DV 诱导的凋亡血小板。然而,在这些患者中,TPO 诱导的增强的血小板生成克服了血小板清除的加速。
临床试验注册
UMIN000004835。