Pugachev Konstantin V, Guirakhoo Farshad, Monath Thomas P
Acambis Inc., 38 Sidney Street, Cambridge, MA 02139, USA.
Curr Opin Infect Dis. 2005 Oct;18(5):387-94. doi: 10.1097/01.qco.0000178823.28585.ad.
Here we review recent epidemiological trends in flavivirus diseases, findings related to existing vaccines, and new directions in flavivirus vaccine research. We emphasize the need for stepped-up efforts to stop further spread and intensification of these infections worldwide.
Although the incidence and geographic distribution of flavivirus diseases have increased in recent years, human vaccines are available only for yellow fever, Japanese encephalitis, tick-borne encephalitis and Kyasanur forest disease. Factors contributing to resurgence include insufficient supplies of available vaccines, incomplete vaccination coverage and relaxation in vector control. Research has been underway for 60 years to develop effective vaccines against dengue, and recent progress is encouraging. The development of vaccines against West Nile, virus recently introduced to North America, has been initiated. In addition, there is considerable interest in improving existing vaccines with respect to increasing safety (e.g. eliminating the newly recognized syndrome of yellow fever vaccine-associated viscerotropic adverse disease), and to reducing the cost and number of doses required for effective immunization.
Traditional approaches to flavivirus vaccines are still employed, while recent advancements in biotechnology produced new approaches to vaccine design, such as recombinant live virus, subunit and DNA vaccines. Live chimeric vaccines against dengue, Japanese encephalitis and West Nile based on yellow fever 17D virus (ChimeriVax) are in phase I/II trials, with encouraging results. Other chimeric dengue, tick-borne encephalitis and West Nile virus candidates were developed based on attenuated dengue backbones. To further reduce the impact of flavivirus diseases, vaccination policies and vector control programs in affected countries require revision.
在此,我们综述黄病毒疾病的近期流行病学趋势、与现有疫苗相关的研究结果以及黄病毒疫苗研究的新方向。我们强调需要加大力度,以阻止这些感染在全球范围内进一步传播和加剧。
尽管近年来黄病毒疾病的发病率和地理分布有所增加,但人类疫苗仅可用于黄热病、日本脑炎、蜱传脑炎和基孔肯雅森林病。导致疫情复发的因素包括现有疫苗供应不足、疫苗接种覆盖率不完整以及病媒控制有所放松。针对登革热研发有效疫苗的研究已经进行了60年,近期取得的进展令人鼓舞。针对最近传入北美的西尼罗河病毒的疫苗研发已经启动。此外,人们对改进现有疫苗也有着浓厚兴趣,旨在提高安全性(例如消除新发现的黄热病疫苗相关内脏嗜性不良反应综合征),并降低有效免疫所需的成本和剂量数量。
黄病毒疫苗仍采用传统方法,而生物技术的最新进展产生了新的疫苗设计方法,如重组活病毒、亚单位和DNA疫苗。基于黄热病17D病毒的登革热、日本脑炎和西尼罗河嵌合活疫苗(ChimeriVax)正处于I/II期试验阶段,结果令人鼓舞。其他基于减毒登革热主干研发的登革热、蜱传脑炎和西尼罗河病毒嵌合候选疫苗也已问世。为了进一步减轻黄病毒疾病的影响,受影响国家的疫苗接种政策和病媒控制计划需要修订。