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Differential onset of apoptosis in avian influenza H5N1 and seasonal H1N1 virus infected human bronchial and alveolar epithelial cells: an in vitro and ex vivo study

机译:禽流感H5N1和季节性H1N1病毒感染的人支气管和肺泡上皮细胞凋亡的不同发作:体外和离体研究

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Human disease caused by highly pathogenic avian influenza (HPAI) H5N1 virus is associated with fulminant viral pneumonia and mortality rates in excess of 60%. Cytokine dysre-gulation is thought to contribute to its pathogenesis. We previously found delayed onset of apoptosis in H5N1 infected human macrophages and, therefore, a longer survival time of the target cells for prolonged virus replication and cytokine and chemokine secretion, which may contribute to the pathogenesis of H5N1 disease in humans.As bronchial and alveolar epithelial cells are target cells of influenza virus because of their proximal physiological location and interaction with macrophages, we further investigated if the differential onset of apoptosis could be found in influenza H5N1 and seasonal influenza H1N1 infected human respiratory epithelia. We dissected the apoptotic pathways triggered by influenza virus infection.
机译:高致病性禽流感(HPAI)H5N1病毒引起的人类疾病与暴发性病毒性肺炎有关,死亡率超过60%。细胞因子失调被认为是其发病机理的原因。我们先前发现被H5N1感染的人类巨噬细胞凋亡的延迟发生,因此靶细胞的存活时间延长,从而延长了病毒复制以及细胞因子和趋化因子的分泌,这可能与人类H5N1疾病的发病机理有关。上皮细胞由于其近端生理位置和与巨噬细胞的相互作用而成为流感病毒的靶细胞,我们进一步研究了是否在H5N1流感和季节性H1N1流感感染的人类呼吸道上皮细胞中发现了凋亡的差异性发作。我们解剖了由流感病毒感染触发的凋亡途径。

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