Apoptotic cell death in response to dengue virus infection: the pathogenesis of dengue haemorrhagic fever revisited

Philippe Marianneau, Marie Flamand, Vincent Deubel, Philippe Desprès
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引用次数: 58

Abstract

Background: Dengue virus infection may be asymptomatic or lead to undifferentiated febrile illness or dengue haemorrhagic fever and dengue shock syndrome (DHF/DSS). The major clinical manifestations of DHF/DSS are high fever, haemorrhage, hepatomegaly and circulatory failure.

Objectives: The relatively high level of viraemia only a few days after infection may reflect a large number of replication sites. However, the degree of cell injury in fatal cases of DHF/DSS is not sufficient to explain death and suggests metabolic disturbance rather than tissue destruction. This theory was investigated in this study.

Results: We demonstrated that replication of dengue virus in infected cells induces stress leading to apoptotic cell death in vitro and in vivo.

Conclusions: The elimination of apoptotic bodies by phagocytic cells is a previously unsuspected pathway of dengue virus clearance from infected tissues. However, the mechanisms of host defence involving apoptosis and phagocytic cell activation may cause local tissue injury or transient homeostasis imbalance and may trigger further deleterious events.

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对登革病毒感染的细胞凋亡反应:登革出血热的发病机制
背景:登革热病毒感染可能无症状或导致未分化的发热性疾病或登革出血热和登革休克综合征(DHF/DSS)。DHF/DSS的主要临床表现为高热、出血、肝肿大和循环衰竭。目的:在感染后几天内相对较高的病毒血症水平可能反映了大量的复制位点。然而,致死性DHF/DSS病例的细胞损伤程度不足以解释死亡,提示代谢紊乱而非组织破坏。本研究对这一理论进行了研究。结果:在体外和体内实验中,我们证明了登革热病毒在感染细胞中的复制可诱导应激导致凋亡细胞死亡。结论:吞噬细胞清除凋亡小体是一种以前未被怀疑的登革热病毒从感染组织中清除的途径。然而,涉及凋亡和吞噬细胞活化的宿主防御机制可能导致局部组织损伤或短暂的稳态失衡,并可能引发进一步的有害事件。
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