Kurane Ichiro
Department of Virology 1, National Institute of Infectious Diseases, 1-23-1 Toyama, Shinjuku-ku, Tokyo 162-8640, Japan.
Comp Immunol Microbiol Infect Dis. 2007 Sep;30(5-6):329-40. doi: 10.1016/j.cimid.2007.05.010. Epub 2007 Jul 23.
Dengue virus infections are a serious cause of morbidity and mortality in most tropical and subtropical areas of the world; Southeast and South Asia, Central and South America, and the Caribbean. Dengue virus infection can be asymptomatic or causes two forms of illness, dengue fever (DF) and dengue hemorrhagic fever (DHF), which is the severe form of dengue illness and often fatal. Pathogenesis of DHF has been analyzed, and two mechanisms are considered to be responsible. These include dengue serotype cross-reactive immune responses and virulence of the virus. The immunopathological mechanisms include a complex series of immune responses. Rapid increase in the levels of cytokines, especially TNF-alpha, and chemical mediators play a key role in inducing unique clinical manifestations of DHF such as plasma leakage, shock, and hemorrhagic manifestations. It is understood that the process is initiated by infection with a virulent dengue virus, often in the presence of antibodies that enhance dengue virus infection in secondary infection, and then triggered by rapidly elevated cytokines and chemical mediators that were produced by intense immune activation. However, complete understanding of the entire pathological mechanism is far from complete, and further studies are still needed.
登革病毒感染是世界上大多数热带和亚热带地区(东南亚、南亚、中美洲、南美洲及加勒比地区)发病和死亡的一个重要原因。登革病毒感染可以没有症状,或者引发两种疾病形式,即登革热(DF)和登革出血热(DHF),后者是登革疾病的严重形式,且往往致命。登革出血热的发病机制已得到分析,有两种机制被认为与之相关。这包括登革病毒血清型交叉反应性免疫应答和病毒的毒力。免疫病理机制包括一系列复杂的免疫应答。细胞因子尤其是肿瘤坏死因子-α水平的迅速升高以及化学介质在引发登革出血热的独特临床表现(如血浆渗漏、休克和出血表现)中起关键作用。据了解,该过程由感染强毒力登革病毒引发,通常是在继发感染时存在增强登革病毒感染的抗体的情况下,然后由强烈免疫激活产生的细胞因子和化学介质迅速升高所触发。然而,对整个病理机制的完全理解还远未完成,仍需要进一步研究。