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Immune responses of a CV-A16 live attenuated candidate strain and its protective effects in rhesus monkeys

Coxsackievirus A16 (CV-A16) is a major causative pathogen of hand, foot, and mouth diseases (HFMDs). The licensed HFMD vaccine targets EV-A71 without cross-protection against CV-A16. Thus, a CV-A16 vaccine is needed. In this study, the immunogenicity and protective efficacy of a live attenuated CV-A...

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Autores principales: Yang, Ting, Xie, Tianhong, Li, Hua, Song, Xia, Yue, Lei, Wang, Xi, Shen, Dong, Ma, Kaili, Jiang, Qinfang, Long, Runxiang, Yang, Rong, He, Xin, Zhang, Ye, Xie, Zhongping, Li, Qihan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7580583/
https://www.ncbi.nlm.nih.gov/pubmed/32930072
http://dx.doi.org/10.1080/22221751.2020.1823889
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author Yang, Ting
Xie, Tianhong
Li, Hua
Song, Xia
Yue, Lei
Wang, Xi
Shen, Dong
Ma, Kaili
Jiang, Qinfang
Long, Runxiang
Yang, Rong
He, Xin
Zhang, Ye
Xie, Zhongping
Li, Qihan
author_facet Yang, Ting
Xie, Tianhong
Li, Hua
Song, Xia
Yue, Lei
Wang, Xi
Shen, Dong
Ma, Kaili
Jiang, Qinfang
Long, Runxiang
Yang, Rong
He, Xin
Zhang, Ye
Xie, Zhongping
Li, Qihan
author_sort Yang, Ting
collection PubMed
description Coxsackievirus A16 (CV-A16) is a major causative pathogen of hand, foot, and mouth diseases (HFMDs). The licensed HFMD vaccine targets EV-A71 without cross-protection against CV-A16. Thus, a CV-A16 vaccine is needed. In this study, the immunogenicity and protective efficacy of a live attenuated CV-A16 candidate, K168-8Ac, were evaluated in a rhesus monkey model. Four passages of this strain (P35, P50, P60, and P70) were administered to monkeys, and its protective effect was identified. The immunized monkeys were clinically asymptomatic, except for slight fever. Weak viraemia was observed, and two doses of vaccination were found to significantly reduce virus shedding. High levels of antibody responses were observed (1:1024–1:2048), along with a significant increase in plasma IL-8. The I.M. group showed a much stronger humoural immunity. Pathological damage was detected mainly in lung tissues, although thalamus, spinal cord, lymph nodes, and livers were involved. After the viral challenge, it was found that two doses of vaccine reduced virus shedding, and the degree of lung damage and the number of organs involved decreased as the passage number increased. Overall, a robust immune response and partial protection against CV-A16, triggered by the K168-8Ac strain, were demonstrated. This study provides valuable data for CV-A16 vaccine development.
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spelling pubmed-75805832020-10-29 Immune responses of a CV-A16 live attenuated candidate strain and its protective effects in rhesus monkeys Yang, Ting Xie, Tianhong Li, Hua Song, Xia Yue, Lei Wang, Xi Shen, Dong Ma, Kaili Jiang, Qinfang Long, Runxiang Yang, Rong He, Xin Zhang, Ye Xie, Zhongping Li, Qihan Emerg Microbes Infect Research Article Coxsackievirus A16 (CV-A16) is a major causative pathogen of hand, foot, and mouth diseases (HFMDs). The licensed HFMD vaccine targets EV-A71 without cross-protection against CV-A16. Thus, a CV-A16 vaccine is needed. In this study, the immunogenicity and protective efficacy of a live attenuated CV-A16 candidate, K168-8Ac, were evaluated in a rhesus monkey model. Four passages of this strain (P35, P50, P60, and P70) were administered to monkeys, and its protective effect was identified. The immunized monkeys were clinically asymptomatic, except for slight fever. Weak viraemia was observed, and two doses of vaccination were found to significantly reduce virus shedding. High levels of antibody responses were observed (1:1024–1:2048), along with a significant increase in plasma IL-8. The I.M. group showed a much stronger humoural immunity. Pathological damage was detected mainly in lung tissues, although thalamus, spinal cord, lymph nodes, and livers were involved. After the viral challenge, it was found that two doses of vaccine reduced virus shedding, and the degree of lung damage and the number of organs involved decreased as the passage number increased. Overall, a robust immune response and partial protection against CV-A16, triggered by the K168-8Ac strain, were demonstrated. This study provides valuable data for CV-A16 vaccine development. Taylor & Francis 2020-09-30 /pmc/articles/PMC7580583/ /pubmed/32930072 http://dx.doi.org/10.1080/22221751.2020.1823889 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group, on behalf of Shanghai Shangyixun Cultural Communication Co., Ltd https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Yang, Ting
Xie, Tianhong
Li, Hua
Song, Xia
Yue, Lei
Wang, Xi
Shen, Dong
Ma, Kaili
Jiang, Qinfang
Long, Runxiang
Yang, Rong
He, Xin
Zhang, Ye
Xie, Zhongping
Li, Qihan
Immune responses of a CV-A16 live attenuated candidate strain and its protective effects in rhesus monkeys
title Immune responses of a CV-A16 live attenuated candidate strain and its protective effects in rhesus monkeys
title_full Immune responses of a CV-A16 live attenuated candidate strain and its protective effects in rhesus monkeys
title_fullStr Immune responses of a CV-A16 live attenuated candidate strain and its protective effects in rhesus monkeys
title_full_unstemmed Immune responses of a CV-A16 live attenuated candidate strain and its protective effects in rhesus monkeys
title_short Immune responses of a CV-A16 live attenuated candidate strain and its protective effects in rhesus monkeys
title_sort immune responses of a cv-a16 live attenuated candidate strain and its protective effects in rhesus monkeys
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7580583/
https://www.ncbi.nlm.nih.gov/pubmed/32930072
http://dx.doi.org/10.1080/22221751.2020.1823889
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