The pre-existing cellular immunity to Japanese encephalitis virus heterotypically protects mice from Zika virus infection

被引:10
|
作者
Zhang, Weihong [1 ,2 ,7 ]
Xu, Yongfen [2 ]
Zhao, Fanfan [2 ,7 ]
Tarbe, Marion [2 ]
Zhou, Shuru [1 ,2 ]
Wang, Weihong [3 ,7 ]
Zhang, Shengyuan [3 ,7 ]
Zhang, Wei [2 ]
Xu, Qiuping [2 ,7 ]
Shi, Lina [2 ,7 ]
Yuan, Feng [2 ,7 ]
Lin, Xinwen [2 ,7 ]
Liu, Shuai [2 ,7 ]
Sun, Jing [4 ]
Zhao, Jincun [4 ]
Yang, Yaling [5 ]
Liang, Xiaozhen [2 ]
Zhong, Jin [2 ]
Long, Gang [2 ]
Qin, Chengfeng [6 ]
Leng, Qibin [2 ,4 ]
Tang, Hong [1 ,2 ]
机构
[1] Chinese Acad Sci, Wuhan Inst Virol, State Key Lab Virol, Wuhan 430071, Peoples R China
[2] Chinese Acad Sci, Inst Pasteur Shanghai, CAS Key Lab Mol Virol & Immunol, Shanghai 200031, Peoples R China
[3] Chinese Acad Sci, Inst Biophys, CAS Key Lab Infect & Immun, Beijing 100101, Peoples R China
[4] Guangzhou Med Univ, Affiliated Canc Hosp & Inst, State Key Lab Resp Dis, Guangzhou 510095, Peoples R China
[5] Fudan Univ, Shanghai Publ Hlth Clin Ctr, Shanghai 201508, Peoples R China
[6] Beijing Inst Microbiol & Epidemiol, Dept Virol, State Key Lab Pathogen & Biosecur, Beijing 100071, Peoples R China
[7] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
关键词
Japanese encephalitis virus; Zika virus; CD8(+) T; Cross protection; ANTIBODY-DEPENDENT ENHANCEMENT; DENGUE VIRUS; CROSS-REACTIVITY; FEVER;
D O I
10.1016/j.scib.2019.11.006
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Zika virus (ZIKV) and Japanese encephalitis virus (JEV) are closely related flaviviruses, ZIKV circulates in the population that has been JEV vaccinated in Southeast Asian countries. This alerts that a pre-existing immunity to JEV would impact ZIKV infection and/or pathogenesis. Herein we showed that the preexisting immunity to JEV SA14-14-2 vaccination provided an ample protection against non-lethal or lethal dose of ZIKV infection in mice. This was in sharp contrast to the passive immunization of JEV antibodies, which failed to affect ZIKV infection or pathogenesis in mice, albeit these antibodies exhibited cross-reactivity and antibody dependent enhancement (ADE) of ZIKV infection in vitro. Furthermore, we determined that JEV vaccine-elicited CD8(+) T cells were required to mediate the heterotypic protection of ZIKV infection, which cross-reacted to ZIKV E and NS5 antigens (E294-302 and NS5(2839-2848)). Adoptive transfer of these CD8(+) T cells could partially protect the mice from ZIKV challenge. Therefore, although short of epidemiological evidence, these results suggested that cross-reactive CD8(+) T cells activated by JEV vaccination could protect potential ZIKV infection in human populations. (C) 2019 Science China Press. Published by Elsevier B.V. and Science China Press. All rights reserved.
引用
收藏
页码:402 / 409
页数:8
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