Advances in Dengue Vaccine: A Review Study

A. Yaro
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Abstract

Dengue virus (DENV) is a vector-borne viral disease that cause more human morbidity and mortality worldwide than any other arthropod-borne virus. It is estimated that 3.97 billion people living in 128 countries are at risk of dengue, 400 million infections annually, and 96 million asymptomatic cases occurring every year [1-4]. Four closely related dengue serotypes cause the disease: DENV-1 to -4. Serotype specific differences in clinical manifestations have been reported. In a cross-sectional study, Balmaseda et al. [5] reported that among hospitalized children in Nicaragua over 3 years period DENV-2 was associated with more shock and internal hemorrhage while DENV-1 was associated with increased vascular permeability. Furthermore, DENV-1 was associated with more hospitalized primary dengue cases and more primary DENV infection with severe manifestations. Others reported that DENV-2 and DENV-3 may cause more severe diseases than the other serotypes and that DENV-4 is associated with milder illness [6-12]. Certain genotypes within particular serotypes are associated with epidemics of dengue hemorrhagic fever (DHF) vs. classic dengue [11,13]. Aedes aegypt mosquitoes are the primary vectors of DENV throughout the tropics [14]. DENV infection is categorized as asymptomatic infection, subclinical infection, undifferentiated fever, dengue fever, DHF with or without dengue shock syndrome (DSS) and other severe forms of dengue. DHF is characterized by fever, bleeding diathesis, and a tendency to develop a potentially fatal shock syndrome. Clinical manifestations of dengue infection range from mild dengue fever to severe plasma leakage with hemorrhagic manifestations. Thrombocytopenia is an important finding in patients with dengue. A study reported that platelet count of dengue patients can be normal or abnormally high or low. This should be used for future diagnosis [15-17]. Management of dengue patient is to have good fluid replacement therapy until recovery of platelet. Multiple factors have been suggested to contribute to severe dengue such as secondary infections, age, viral load and infecting serotype and genotype [6-8]. Dengue infection is spreading at an alarming rate around the globe and statistics shows that the disease has increased dramatically since 1980, with epidemics occurring in both eastern and western Africa [18,19]. The WHO statistics indicates that 2.4% of the global burden of dengue hemorrhagic fever is in Africa and one-fifth of the populations are at risk [17].
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登革热疫苗研究进展综述
登革热病毒(DENV)是一种媒介传播的病毒性疾病,在世界范围内引起的人类发病率和死亡率高于任何其他节肢动物传播的病毒。据估计,生活在128个国家的39.7亿人面临登革热风险,每年有4亿人感染登革热,每年发生9600万无症状病例[1-4]。四种密切相关的登革热血清型可引起该病:DENV-1至-4。临床表现的血清型特异性差异已有报道。Balmaseda等人在一项横断面研究中报道,在尼加拉瓜3年住院儿童中,DENV-2与更多休克和内出血相关,而DENV-1与血管通透性增加相关。此外,DENV-1与更多住院原发性登革热病例和更多具有严重症状的原发性登革热感染有关。也有报道称,DENV-2和DENV-3可能比其他血清型引起更严重的疾病,而DENV-4与较轻的疾病相关[6-12]。特定血清型中的某些基因型与登革出血热(DHF)与经典登革热的流行相关[11,13]。在整个热带地区,埃及伊蚊是登革热病毒的主要传播媒介。登革出血热感染分为无症状感染、亚临床感染、未分化热、登革热、登革出血热伴或不伴登革休克综合征(DSS)和其他严重形式的登革热。DHF的特点是发热,出血,并有发展为潜在致命休克综合征的倾向。登革热感染的临床表现从轻度登革热到严重的血浆漏出并伴有出血性表现。血小板减少症是登革热患者的一个重要发现。一项研究报道,登革热患者的血小板计数可正常或异常高或低。这应该用于未来的诊断[15-17]。对登革热患者的处理是进行良好的补液治疗,直至血小板恢复。继发性感染、年龄、病毒载量、感染血清型和基因型等多种因素被认为是导致重症登革热的因素[6-8]。登革热感染正以惊人的速度在全球蔓延,统计数据显示,自1980年以来,该疾病急剧增加,在东非和西非都发生了流行[18,19]。世卫组织的统计数据表明,全球登革热出血热负担的2.4%在非洲,五分之一的人口处于危险之中。
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