DNA vaccine encoding central conserved region of G protein induces Th1 predominant immune response and protection from RSV infection in mice

被引:10
|
作者
Hua, Ying [1 ]
Jiao, Yue-Ying [1 ]
Ma, Yao [1 ]
Peng, Xiang-Lei [1 ]
Fu, Yuan-Hui [1 ]
Zheng, Yan-Peng [1 ]
Hong, Tao [1 ]
He, Jin-Sheng [1 ]
机构
[1] Beijing Jiaotong Univ, Coll Life Sci & Bioengn, 3 Shangyuan Cun, Beijing 100044, Peoples R China
关键词
RSV; G glycoprotein; CX3C; DNA vaccine; RESPIRATORY SYNCYTIAL VIRUS; G FUSION PROTEIN; ENHANCED DISEASE; G-GLYCOPROTEIN; INTRANASAL IMMUNIZATION; BALB/C MICE; CHALLENGE; BBG2NA; ANTIBODIES; PATHOLOGY;
D O I
10.1016/j.imlet.2016.09.011
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Human respiratory syncytial virus (RSV) can cause serious infection in the lower respiratory tract, especially in infants, young children, the elderly and the immunocompromised population worldwide. Previous study demonstrated the polypeptide (amino acids 148-198) of RSV attachment (G) glycoprotein, corresponding to the central conserved region and encompassing CX3C chemokine motif, could induce antibodies and protection from RSV challenge in mice [1,2]. In this study, we evaluated the immune efficacy of the recombinant DNA vaccine of pVAX1/3G(148-198) encoding RSV G protein polypeptide. RSV specific serum IgG antibodies with neutralizing activity were stimulated following prime-boost immunization of pVAX1/3G(148-198) intramuscularly, and the ratio of IgG2a/IgG1 was 4.93, indicating a Th1 biased immune response. After challenged intranasally with RSV Long, the vaccinated mice showed both decreased lung RSV titers, pulmonary inflammation and body weight loss. The results suggest that pVAX1/3G(148-198) DNA vaccine may be an effective RSV vaccine candidate, and deserves further exploration. (C) 2016 European Federation of Immunological Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:95 / 101
页数:7
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