Heterotypic Dengue Infection with Live Attenuated Monotypic Dengue Virus Vaccines: Implications for Vaccination of Populations in Areas Where Dengue Is Endemic

被引:39
作者
Durbin, Anna P. [1 ]
Schmidt, Alexander [2 ]
Elwood, Dan [1 ]
Wanionek, Kimberli A. [1 ]
Lovchik, Janece [1 ]
Thumar, Bhavin [1 ]
Murphy, Brian R. [2 ]
Whitehead, Stephen S. [1 ]
机构
[1] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Int Hlth, Ctr Immunizat Res, Baltimore, MD USA
[2] NIAID, Infect Dis Lab, Bethesda, MD 20892 USA
基金
美国国家卫生研究院;
关键词
HEMORRHAGIC-FEVER; NAIVE ADULTS; ANTIBODY; ENHANCEMENT; CANDIDATE; VIREMIA; VOLUNTEERS; SEVERITY; DISEASE; GREECE;
D O I
10.1093/infdis/jiq059
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Because infection with any of the 4 Dengue virus serotypes may elicit both protective neutralizing antibodies and nonneutralizing antibodies capable of enhancing subsequent heterotypic Dengue virus infections, the greatest risk for severe dengue occurs during a second, heterotypic Dengue virus infection. It remains unclear whether the replication of live attenuated vaccine viruses will be similarly enhanced when administered to Dengue-immune individuals. Methods. We recruited 36 healthy adults who had previously received a monovalent live Dengue virus vaccine 0.6-7.4 years earlier. Participants were assigned to 1 of 4 cohorts and were randomly chosen to receive placebo or a heterotypic vaccine. The level of replication, safety, and immunogenicity of the heterotypic vaccine virus was compared with that of Dengue virus immunologically naive vaccinees. Results. Vaccine virus replication and reactogenicity after monovalent Dengue virus vaccination in naive and heterotypically immune vaccinees was similar. In contrast to naive vaccinees, the antibody response in heterotypically immune vaccinees was broadly neutralizing and mimicked the response observed by natural secondary Dengue virus infection. Conclusions. Enhanced replication of these live attenuated Dengue virus vaccines was minimal in heterotypically immune vaccinees and suggests that the further evaluation of these candidate vaccines in populations with preexisting DENV immunity can proceed safely.
引用
收藏
页码:327 / 334
页数:8
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