Bridging Efficacy of a Tetravalent Dengue Vaccine from Children/Adolescents to Adults in Highly Endemic Countries Based on Neutralizing Antibody Response

被引:11
|
作者
Gilbert, Peter B. [1 ,2 ,8 ]
Huang, Ying [1 ,2 ,8 ]
Juraska, Michal [1 ]
Moodie, Zoe [1 ]
Fong, Youyi [1 ,2 ,8 ]
Luedtke, Alexander [1 ]
Zhuang, Yingying [2 ]
Shao, Jason [1 ]
Carpp, Lindsay N. [1 ]
Jackson, Nicholas [3 ]
Chambonneau, Laurent [4 ]
Bouckenooghe, Alain [5 ]
Zambrano, Betzana [6 ]
Frago, Carina [5 ]
Pallardy, Sophie [4 ]
Noriega, Fernando [7 ]
机构
[1] Fred Hutchinson Canc Res Ctr, Vaccine & Infect Dis Div, 1100 Fairview Ave North, Seattle, WA 98109 USA
[2] Univ Washington, Dept Biostat, Seattle, WA 98195 USA
[3] Sanofi Pasteur, Res & Non Clin Safety, Marcy Letoile, France
[4] Sanofi Pasteur, Clin Programs, Marcy Letoile, France
[5] Sanofi Pasteur, Clin Sci, Singapore, Singapore
[6] Sanofi Pasteur, Clin Sci, Montevideo, Uruguay
[7] Sanofi Pasteur, Clin Sci, Swiftwater, PA USA
[8] Univ Washington, Fred Hutchinson Canc Res Ctr, Vaccine & Infect Dis Div, Seattle, WA 98195 USA
来源
基金
美国国家卫生研究院;
关键词
T-CELLS; HEALTHY-ADULTS; PROTECTION; SEROPREVALENCE; INFECTION; CHILDREN; CORRELATE; SAFETY; TITERS; RISK;
D O I
10.4269/ajtmh.18-0534
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
The CYD-TDV vaccine is licensed in multiple endemic countries based on vaccine efficacy (VE) against symptomatic, virologically confirmed dengue demonstrated in two phase 3 trials (CYD14, 2- to 14-year-olds, Asia; CYD15, 9- to 16-year-olds, Latin America). 50% plaque reduction neutralization test (PRNT50) titers at baseline and month 13 (post-vaccination) were associated with VE and may enable bridging VE to adults. Two phase 2 trials of CYD-TDV measured baseline and month 13 PRNT50 titers: CYD22 (9- to 45-year-olds, Vietnam) and CYD47 (18- to 45-year-olds, India). 50% plaque reduction neutralization test distributions were compared between age cohorts, and four versions of an epidemiological bridging method were used to estimate VE against any serotype (dengue virus [DENV]-Any) and against each serotype over 25 months post first vaccination in a hypothetical CYD14 + CYD15 18- to 45-year-old cohort (bridging population 1) and in the actual CYD47 18- to 45-year-old cohort (bridging population 2). Baseline and month 13 geometric mean PRNT50 titers to each serotype were significantly greater in 18- to 45-year-olds than 9- to 16-year-olds for all comparisons. The four methods estimated VE against DENV-Any at 75.3-86.0% (95% CIs spanning 52.5-100%) for bridging population 1 and 68.4-77.5% (95% CIs spanning 42.3-88.5%) for bridging population 2. The vaccine efficacy against serotype 1, 2, 3, and 4 was estimated at 56.9-76.9%, 68.3-85.8%, 91.4-95.0%, and 93.2-100% (bridging population 1) and 44.5-66.9%, 53.2-69.2%, 79.8-92.0%, and 90.6-95.0% (bridging population 2), respectively; thus, CYD-TDV would likely confer improved efficacy in adults than 9- to 16-year-olds. Using the same methods, we predicted VE against hospitalized DEN-Any over 72 months of follow-up, with estimates 59.1-73.5% (95% CIs spanning 40.9-92.2%) for bridging population 1 and 50.9-65.9% (95% CIs spanning 38.1-82.1%) for bridging population 2.
引用
收藏
页码:164 / 179
页数:16
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