Immunogenicity and Protective Efficacy of Aerosolized Live-Attenuated Yellow Fever 17D Vaccine in Mice

被引:0
作者
Zhu, Feng [1 ,2 ]
Sun, Meng-Xu [2 ]
Zhao, Suo-Qun [2 ]
Qin, Cheng-Feng [2 ]
Wang, Jin-Hua [1 ]
Deng, Yong-Qiang [2 ]
机构
[1] Southwest Forestry Univ, Sch Life Sci, Kunming 650224, Peoples R China
[2] Beijing Inst Microbiol & Epidemiol, State Key Lab Pathogen & Biosecur, AMMS, Beijing 100071, Peoples R China
关键词
yellow fever virus; aerosol; immunization route; immunogenicity; protective efficacy; DELIVERY;
D O I
10.3390/vaccines12080856
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Yellow fever (YF), caused by the yellow fever virus (YFV), continually spreads and causes epidemics worldwide, posing a great threat to human health. The live-attenuated YF 17D vaccine (YF-17D) has been licensed for preventing YFV infection and administrated via the intramuscular (i.m.) route. In this study, we sought to determine the immunogenicity and protective efficacy of aerosolized YF-17D via the intratracheal (i.t.) route in mice. YF-17D stocks in liquids were successfully aerosolized into particles of 6 mu m. Further in vitro phenotype results showed the aerosolization process did not abolish the infectivity of YF-17D. Meanwhile, a single i.t. immunization with aerosolized YF-17D induced robust humoral and cellular immune responses in A129 mice, which is comparable to that received i.p. immunization. Notably, the aerosolized YF-17D also triggered specific secretory IgA (SIgA) production in bronchoalveolar lavage. Additionally, all immunized animals survived a lethal dose of YFV challenge in mice. In conclusion, our results support further development of aerosolized YF-17D in the future.
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页数:11
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