Pigs Immunized with the Virus-like Particle Vaccine Are Protected against the Hepatitis E-3 Virus

被引:8
作者
Go, Hyeon-Jeong [1 ]
Park, Byung-Joo [1 ]
Ahn, Hee-Seop [1 ]
Kim, Dong-Hwi [1 ]
Kim, Da-Yoon [1 ]
Kim, Jae-Hyeong [1 ]
Lee, Joong-Bok [1 ]
Park, Seung-Yong
Song, Chang-Seon [1 ]
Lee, Sang-Won [1 ]
Choi, Yang-Kyu [2 ]
Choi, In-Soo [1 ]
机构
[1] Konkuk Univ, Dept Infect Dis, Coll Vet Med, 120 Neundong Ro, Seoul 05029, South Korea
[2] Konkuk Univ, Dept Lab Anim Med, Coll Vet Med, 120 Neundong Ro, Seoul 05029, South Korea
关键词
Hepatitis E virus; virus-like particle; 239 amino acids; viremia; fecal viral shedding; liver fibrosis; baculovirus expression system; EXPRESSION; SEQUENCES; EFFICACY; SAFETY;
D O I
10.3390/vaccines9111265
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In this study, we generated the HEV virus-like particle (VLP) vaccine expressing 239 amino acids (367-605 aa) of the HEV-3 ORF2 using the baculovirus expression system. The HEV-3-239-VLP vaccine efficacy was evaluated by dividing 12 pathogen-free pigs into four groups: negative control, positive control, 100 mu g VLP-, and 200 mu g VLP-vaccinated groups for 10 weeks. The pigs in either of the vaccinated groups were administered the corresponding first and booster doses on weeks 0 and 2. At week 4, the positive control and two vaccinated groups were challenged with 10(6) HEV-3 genomic equivalent copies; viremia and fecal shedding of the virus were identified in pigs in the positive control and 100 mu g VLP-vaccinated pigs showed transient viremia and fecal viral shedding. However, no viruses were detected in the serum or fecal samples of the 200 mu g VLP-vaccinated pigs. The 100 and 200 mu g VLP-vaccinated pigs had significantly higher (p < 0.01) anti-HEV antibodies than the negative control pigs from weeks 6-10 with normal levels of liver enzymes. The 200 mu g VLP-vaccinated pigs showed statistically less liver tissue fibrosis (p < 0.05) than that of the positive control pigs. Thus, the novel baculovirus expression system-generated VLP vaccine dose-dependently protects against HEV-3 challenge and may be useful in other animal species, including humans.
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页数:12
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