Current status and future prospects of yellow fever vaccines

被引:62
作者
Beck, Andrew S. [1 ]
Barrett, Alan D. T. [1 ,2 ,3 ]
机构
[1] Univ Texas Med Branch, Dept Pathol, Galveston, TX 77555 USA
[2] Univ Texas Med Branch, Sealy Ctr Vaccine Dev, Galveston, TX 77555 USA
[3] Univ Texas Med Branch, WHO, Collaborating Ctr Vaccine Res Evaluat & Training, Galveston, TX 77555 USA
基金
美国国家卫生研究院;
关键词
empiric; empiric vaccine; flavivirus; live-attenuated; primary seed; rational vaccine; recombinant vaccine; secondary seed; vaccine; viral diversity; yellow fever virus; INDIAN RHESUS MACAQUES; T-CELL RESPONSES; VISCEROTROPIC DISEASE; VIRAL DISSEMINATION; VIRUS-VACCINE; DOUBLE-BLIND; PHASE-III; 17D; IMMUNOGENICITY; SAFETY;
D O I
10.1586/14760584.2015.1083430
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Yellow fever 17D vaccine is one of the oldest live-attenuated vaccines in current use that is recognized historically for its immunogenic and safe properties. These unique properties of 17D are presently exploited in rationally designed recombinant vaccines targeting not only flaviviral antigens but also other pathogens of public health concern. Several candidate vaccines based on 17D have advanced to human trials, and a chimeric recombinant Japanese encephalitis vaccine utilizing the 17D backbone has been licensed. The mechanism(s) of attenuation for 17D are poorly understood; however, recent insights from large in silico studies have indicated particular host genetic determinants contributing to the immune response to the vaccine, which presumably influences the considerable durability of protection, now in many cases considered to be lifelong. The very rare occurrence of severe adverse events for 17D is discussed, including a recent fatal case of vaccine-associated viscerotropic disease.
引用
收藏
页码:1479 / 1492
页数:14
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