Japanese Encephalitis Virus Vaccination Elicits Cross-Reactive HLA-Class I-Restricted CD8 T Cell Response Against Zika Virus Infection

Japanese encephalitis virus (JEV) exposure or vaccination could elicit cross-reactive CD8 T cell immunity against heterologous flaviviruses in humans. In addition, cross-reactive CD8 T cells induced by dengue virus (DENV) have been shown to play a protective role against Zika virus (ZIKV). However,...

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Main Authors: Marion Tarbe, Wei Dong, Guang Hu, Yongfen Xu, Jing Sun, Solene Grayo, Xianyang Chen, Chengfeng Qin, Jincun Zhao, Li Liu, Xiuzhen Li, Qibin Leng
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-09-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fimmu.2020.577546/full
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author Marion Tarbe
Marion Tarbe
Wei Dong
Guang Hu
Guang Hu
Yongfen Xu
Yongfen Xu
Jing Sun
Solene Grayo
Solene Grayo
Xianyang Chen
Chengfeng Qin
Jincun Zhao
Li Liu
Li Liu
Xiuzhen Li
Xiuzhen Li
Qibin Leng
Qibin Leng
Qibin Leng
author_facet Marion Tarbe
Marion Tarbe
Wei Dong
Guang Hu
Guang Hu
Yongfen Xu
Yongfen Xu
Jing Sun
Solene Grayo
Solene Grayo
Xianyang Chen
Chengfeng Qin
Jincun Zhao
Li Liu
Li Liu
Xiuzhen Li
Xiuzhen Li
Qibin Leng
Qibin Leng
Qibin Leng
author_sort Marion Tarbe
collection DOAJ
description Japanese encephalitis virus (JEV) exposure or vaccination could elicit cross-reactive CD8 T cell immunity against heterologous flaviviruses in humans. In addition, cross-reactive CD8 T cells induced by dengue virus (DENV) have been shown to play a protective role against Zika virus (ZIKV). However, how JEV exposure or vaccination affects ZIKV infection in humans remains unclear. In this report, epitope prediction algorithms were used to predict the cross-reactive CD8 T cell epitope restricted to human HLA between JEV and ZIKV. We found that these predicted CD8 T cell epitopes are immunogenic and cross-reactive in humanized HLA transgenic mice. Moreover, JEV vaccine immunization provided cross-protection against ZIKV infection. Furthermore, CD8 T cells were involved in the protection against ZKIV infection in vivo. Our results have an important clinical implication that vaccination with JEV SA14-14-2 may provide protection against ZIKV infection in humans.
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spelling doaj.art-6e848f18e8804498bee941d87edd50d02022-12-22T01:30:19ZengFrontiers Media S.A.Frontiers in Immunology1664-32242020-09-011110.3389/fimmu.2020.577546577546Japanese Encephalitis Virus Vaccination Elicits Cross-Reactive HLA-Class I-Restricted CD8 T Cell Response Against Zika Virus InfectionMarion Tarbe0Marion Tarbe1Wei Dong2Guang Hu3Guang Hu4Yongfen Xu5Yongfen Xu6Jing Sun7Solene Grayo8Solene Grayo9Xianyang Chen10Chengfeng Qin11Jincun Zhao12Li Liu13Li Liu14Xiuzhen Li15Xiuzhen Li16Qibin Leng17Qibin Leng18Qibin Leng19The Joint Center for Infection and Immunity, Guangzhou Institute of Pediatrics, Guangzhou Women and Children’s Medical Center, Guangzhou Medical University, Guangzhou, ChinaInstitut Pasteur of Shanghai, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai, ChinaAffiliated Cancer Hospital & Institute of Guangzhou Medical University, State Key Laboratory of Respiratory Disease, Guangzhou, ChinaThe Joint Center for Infection and Immunity, Guangzhou Institute of Pediatrics, Guangzhou Women and Children’s Medical Center, Guangzhou Medical University, Guangzhou, ChinaInstitut Pasteur of Shanghai, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai, ChinaThe Joint Center for Infection and Immunity, Guangzhou Institute of Pediatrics, Guangzhou Women and Children’s Medical Center, Guangzhou Medical University, Guangzhou, ChinaInstitut Pasteur of Shanghai, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai, ChinaState Key Laboratory of Respiratory Disease, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, ChinaThe Joint Center for Infection and Immunity, Guangzhou Institute of Pediatrics, Guangzhou Women and Children’s Medical Center, Guangzhou Medical University, Guangzhou, ChinaInstitut Pasteur of Shanghai, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai, ChinaAffiliated Cancer Hospital & Institute of Guangzhou Medical University, State Key Laboratory of Respiratory Disease, Guangzhou, ChinaDepartment of Virology, State Key Laboratory of Pathogens and Biosecurity, Beijing Institute of Microbiology and Epidemiology, Beijing, ChinaState Key Laboratory of Respiratory Disease, Guangzhou Institute of Respiratory Health, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, ChinaThe Joint Center for Infection and Immunity, Guangzhou Institute of Pediatrics, Guangzhou Women and Children’s Medical Center, Guangzhou Medical University, Guangzhou, ChinaInstitut Pasteur of Shanghai, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai, ChinaThe Joint Center for Infection and Immunity, Guangzhou Institute of Pediatrics, Guangzhou Women and Children’s Medical Center, Guangzhou Medical University, Guangzhou, ChinaInstitut Pasteur of Shanghai, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai, ChinaThe Joint Center for Infection and Immunity, Guangzhou Institute of Pediatrics, Guangzhou Women and Children’s Medical Center, Guangzhou Medical University, Guangzhou, ChinaInstitut Pasteur of Shanghai, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai, ChinaAffiliated Cancer Hospital & Institute of Guangzhou Medical University, State Key Laboratory of Respiratory Disease, Guangzhou, ChinaJapanese encephalitis virus (JEV) exposure or vaccination could elicit cross-reactive CD8 T cell immunity against heterologous flaviviruses in humans. In addition, cross-reactive CD8 T cells induced by dengue virus (DENV) have been shown to play a protective role against Zika virus (ZIKV). However, how JEV exposure or vaccination affects ZIKV infection in humans remains unclear. In this report, epitope prediction algorithms were used to predict the cross-reactive CD8 T cell epitope restricted to human HLA between JEV and ZIKV. We found that these predicted CD8 T cell epitopes are immunogenic and cross-reactive in humanized HLA transgenic mice. Moreover, JEV vaccine immunization provided cross-protection against ZIKV infection. Furthermore, CD8 T cells were involved in the protection against ZKIV infection in vivo. Our results have an important clinical implication that vaccination with JEV SA14-14-2 may provide protection against ZIKV infection in humans.https://www.frontiersin.org/article/10.3389/fimmu.2020.577546/fullJEVZikacross-reactiveepitopeCD8 T cellsHLA-A2 transgenic mice
spellingShingle Marion Tarbe
Marion Tarbe
Wei Dong
Guang Hu
Guang Hu
Yongfen Xu
Yongfen Xu
Jing Sun
Solene Grayo
Solene Grayo
Xianyang Chen
Chengfeng Qin
Jincun Zhao
Li Liu
Li Liu
Xiuzhen Li
Xiuzhen Li
Qibin Leng
Qibin Leng
Qibin Leng
Japanese Encephalitis Virus Vaccination Elicits Cross-Reactive HLA-Class I-Restricted CD8 T Cell Response Against Zika Virus Infection
Frontiers in Immunology
JEV
Zika
cross-reactive
epitope
CD8 T cells
HLA-A2 transgenic mice
title Japanese Encephalitis Virus Vaccination Elicits Cross-Reactive HLA-Class I-Restricted CD8 T Cell Response Against Zika Virus Infection
title_full Japanese Encephalitis Virus Vaccination Elicits Cross-Reactive HLA-Class I-Restricted CD8 T Cell Response Against Zika Virus Infection
title_fullStr Japanese Encephalitis Virus Vaccination Elicits Cross-Reactive HLA-Class I-Restricted CD8 T Cell Response Against Zika Virus Infection
title_full_unstemmed Japanese Encephalitis Virus Vaccination Elicits Cross-Reactive HLA-Class I-Restricted CD8 T Cell Response Against Zika Virus Infection
title_short Japanese Encephalitis Virus Vaccination Elicits Cross-Reactive HLA-Class I-Restricted CD8 T Cell Response Against Zika Virus Infection
title_sort japanese encephalitis virus vaccination elicits cross reactive hla class i restricted cd8 t cell response against zika virus infection
topic JEV
Zika
cross-reactive
epitope
CD8 T cells
HLA-A2 transgenic mice
url https://www.frontiersin.org/article/10.3389/fimmu.2020.577546/full
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