Immunogenicity of the Inactivated Japanese Encephalitis Virus Vaccine IXIARO in Children From a Japanese Encephalitis Virus-endemic Region

被引:12
作者
Dubischar, Katrin L. [1 ]
Kadlecek, Vera [1 ]
Sablan, Benjamin [2 ]
Borja-Tabora, Charissa Fay [3 ]
Gatchalian, Salvacion [4 ,5 ]
Eder-Lingelbach, Susanne [1 ]
Kiermayr, Sigrid [1 ]
Spruth, Martin [1 ]
Westritschnig, Kerstin [1 ]
机构
[1] Valneva Austria Gmbh, Campus Vicuna Bioctr 3, A-1030 Vienna, Austria
[2] Univ Philippines, Dept Pediat, Manila, Philippines
[3] Res Inst Trop Med, Dept Hlth, Manila, Philippines
[4] Univ Philippines, Sect Infect & Trop Dis, Dept Pediat, Coll Med,Philippine Gen Hosp, Manila, Philippines
[5] Res Inst Trop Med, Dept Hlth, Muntinlupa, Philippines
关键词
Japanese encephalitis vaccine; immunogenicity; children; IXI-ARO; IC51; SAFETY; BLIND;
D O I
10.1097/INF.0000000000001615
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: Japanese encephalitis (JE) is a major public health concern in Asia and poses a small but potentially fatal threat to travelers from nonendemic countries, including children. No JE vaccine for pediatric use has been available in Europe and the United States. Methods: Age-stratified cohorts of children between 2 months and 17 years received 2 doses of Vero cell-derived inactivated JE virus vaccine (IXIARO; Valneva Austria GmbH, Vienna, Austria) administered 28 days apart [< 3 years, 0.25 mL (half adult dose); >= 3 years, 0.5 mL (full adult dose)]. Immunogenicity endpoints were seroconversion rate, 4-fold increase in JE neutralizing antibody titer and geometric mean titer assessed 56 days and 7 months after the first vaccination in 496 subjects of the intent-to-treat population. The immune response to JE virus at both time points was also analyzed according to prevaccination JE virus and dengue virus serostatus. Results: At day 56, seroconversion was attained in >= 99.2% of subjects with age-appropriate dosing, 4-fold increases in titer were reported for 77.4%100% in various age groups, and geometric mean titers ranged from 176 to 687, with younger children having the strongest immune response. At month 7, seroconversion was maintained in 85.5%-100% of subjects. Pre-existing JE virus immunity did not impact on immune response at day 56; however, it led to a better persistence of protective antibody titers at month 7. Conclusions: IXIARO is highly immunogenic at both doses tested in the pediatric population, leading to protective antibody titers at day 56 in > 99% of subjects who received the age-appropriate dose.
引用
收藏
页码:898 / 904
页数:7
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