Limonta Daniel, Torrentes-Carvalho Amanda, Marinho Cíntia Ferreira, de Azeredo Elzinandes Leal, de Souza Luiz José, Motta-Castro Ana Rita C, da Cunha Rivaldo Venâncio, Kubelka Claire Fernandes, Nogueira Rita Maria Ribeiro, de-Oliveira-Pinto Luzia Maria
Laboratório de Imunologia Viral, Instituto Oswaldo Cruz (IOC), FIOCRUZ, Rio de Janeiro, Brasil; Laboratório de Flavivírus, Instituto Oswaldo Cruz (IOC), FIOCRUZ, Rio de Janeiro, Brasil.
J Med Virol. 2014 Aug;86(8):1437-47. doi: 10.1002/jmv.23832. Epub 2013 Oct 29.
Despite being the most significant arboviral disease worldwide, dengue has no antiviral treatment or reliable severity predictors. It has been shown that apoptotic cells from blood and tissues may be involved in the complex pathogenesis of dengue. However, very little is known about the interplay between proapoptotic and antiapoptotic mediators in this disease. Therefore, plasma levels of the three proapoptotic mediators Fas ligand (FasL), tumor necrosis factor-α (TNF-α), and TNF-related apoptosis-inducing ligand (TRAIL) were measured in dengue patients. Patients were classified according to the World Health Organization classification of dengue revised in 2009. Additionally, inhibitors of apoptosis protein (IAPs) were determined in plasma (Survivin) and peripheral blood mononuclear cells (PBMCs) lysates (cIAP-1, cIAP-2, XIAP). Levels of apoptotic proteins in plasma were correlated with counts of blood cells. FasL and TRAIL levels were elevated in dengue patients without warning signs when compared to patients with severe dengue and controls. Dengue patients with warning signs showed decreased levels of Survivin compared to patients with severe dengue and controls. TRAIL was inversely correlated with counts of lymphocyte subsets. In contrast, Survivin was positively correlated with leukocyte counts. There was a trend of elevated IAPs levels in PBMCs of patients with severe dengue. The results suggest a likely antiviral effect of TRAIL in dengue. It appears that TRAIL might be involved with apoptosis induction of lymphocytes, whereas IAPs might participate in protecting leukocytes from apoptosis. Further research is needed to explore the interactions between pro and antiapoptotic molecules and their implications in dengue pathogenesis.
尽管登革热是全球最重要的虫媒病毒病,但目前尚无抗病毒治疗方法或可靠的病情严重程度预测指标。已有研究表明,血液和组织中的凋亡细胞可能参与登革热复杂的发病机制。然而,对于该疾病中促凋亡和抗凋亡介质之间的相互作用,我们知之甚少。因此,我们检测了登革热患者血浆中三种促凋亡介质Fas配体(FasL)、肿瘤坏死因子-α(TNF-α)和TNF相关凋亡诱导配体(TRAIL)的水平。患者根据世界卫生组织2009年修订的登革热分类标准进行分类。此外,还测定了血浆中凋亡抑制蛋白(IAPs)(生存素)以及外周血单个核细胞(PBMCs)裂解物中(细胞凋亡抑制蛋白-1、细胞凋亡抑制蛋白-2、X连锁凋亡抑制蛋白)的水平。血浆中凋亡蛋白水平与血细胞计数相关。与重症登革热患者和对照组相比,无预警信号的登革热患者FasL和TRAIL水平升高。有预警信号的登革热患者与重症登革热患者和对照组相比,生存素水平降低。TRAIL与淋巴细胞亚群计数呈负相关。相反,生存素与白细胞计数呈正相关。重症登革热患者PBMCs中IAPs水平有升高趋势。结果表明TRAIL在登革热中可能具有抗病毒作用。似乎TRAIL可能参与淋巴细胞的凋亡诱导,而IAPs可能参与保护白细胞免于凋亡。需要进一步研究来探索促凋亡和抗凋亡分子之间的相互作用及其在登革热发病机制中的意义。