Limonta Daniel, Capó Virginia, Torres Griselda, Pérez Ana B, Guzmán María G
Virology Department, PAHO/WHO Collaborating Center for the Study of Dengue and its Vector, Havana, Cuba.
J Clin Virol. 2007 Sep;40(1):50-4. doi: 10.1016/j.jcv.2007.04.024. Epub 2007 Aug 10.
Apoptosis, or programmed cell death, has been implicated in dengue hemorrhagic fever/dengue shock syndrome (DHF/DSS) pathogenesis.
To determine the in vivo apoptosis contribution to the pathogenesis of fatal DHF/DSS during a Cuban dengue epidemic.
We detected apoptosis by the TdT-mediated dUTP Nick-End Labeling (TUNEL) technique and dengue virus (DENV) antigens by an immunohistochemical assay in different tissues from six individuals who died of DHF/DSS during the Santiago de Cuba DENV-2 epidemic in 1997.
DENV antigens were immunolocalized mainly in hepatocytes. Apoptotic cells were found in five of the six cases studied. Apoptosis was demonstrated in liver, brain, intestinal and lung tissues. Severe brain hypoxia and ischemia in the studied subjects during DHF/DSS probably might induce apoptosis in cerebral cells. Apoptotic microvascular endothelial cells (ECs) in pulmonary and intestinal tissues, a finding only previously reported in vitro, are likely related to vascular plasma leakage manifested by the individuals.
Apoptosis was demonstrated in cerebral cells, white blood cells, intestinal and pulmonary microvascular ECs from Cuban fatal cases of DHF/DSS. As far as we know, these findings have not been previously reported in DHF/DSS. Our results indicate there is very likely an in vivo contribution of apoptosis to the pathophysiological mechanisms of DHF/DSS.
细胞凋亡,即程序性细胞死亡,与登革出血热/登革休克综合征(DHF/DSS)的发病机制有关。
确定在古巴登革热流行期间,体内细胞凋亡对致命性DHF/DSS发病机制的作用。
我们采用TdT介导的dUTP缺口末端标记(TUNEL)技术检测细胞凋亡,并通过免疫组织化学分析检测1997年圣地亚哥德古巴登革热病毒2型流行期间死于DHF/DSS的6名个体不同组织中的登革热病毒(DENV)抗原。
DENV抗原主要定位于肝细胞。在所研究的6例病例中,有5例发现了凋亡细胞。在肝脏、脑、肠道和肺组织中均证实有细胞凋亡。DHF/DSS期间所研究对象的严重脑缺氧和缺血可能会诱导脑细胞凋亡。肺和肠道组织中凋亡的微血管内皮细胞(ECs),这一发现此前仅在体外有报道,可能与个体表现出的血管血浆渗漏有关。
在古巴致命性DHF/DSS病例的脑细胞、白细胞、肠道和肺微血管ECs中均证实有细胞凋亡。据我们所知,这些发现此前在DHF/DSS中尚未见报道。我们的结果表明,细胞凋亡很可能在体内对DHF/DSS的病理生理机制有影响。