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Maternal vaccination and protective immunity against Zika virus vertical transmission
An important goal of the Zika virus (ZIKV) vaccine is to prevent a congenital syndrome in fetuses of pregnant women, but studies directly evaluating maternal vaccination for ZIKV are lacking. Here we report maternal vaccination using a live-attenuated ZIKV vaccine (3ʹUTR-∆10-LAV) in a pregnant mouse...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6908683/ https://www.ncbi.nlm.nih.gov/pubmed/31831806 http://dx.doi.org/10.1038/s41467-019-13589-1 |
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author | Shan, Chao Xie, Xuping Luo, Huanle Muruato, Antonio E. Liu, Yang Wakamiya, Maki La, Jun-Ho Chung, Jin Mo Weaver, Scott C. Wang, Tian Shi, Pei-Yong |
author_facet | Shan, Chao Xie, Xuping Luo, Huanle Muruato, Antonio E. Liu, Yang Wakamiya, Maki La, Jun-Ho Chung, Jin Mo Weaver, Scott C. Wang, Tian Shi, Pei-Yong |
author_sort | Shan, Chao |
collection | PubMed |
description | An important goal of the Zika virus (ZIKV) vaccine is to prevent a congenital syndrome in fetuses of pregnant women, but studies directly evaluating maternal vaccination for ZIKV are lacking. Here we report maternal vaccination using a live-attenuated ZIKV vaccine (3ʹUTR-∆10-LAV) in a pregnant mouse model. Maternal immunization with 3ʹUTR-∆10-LAV does not cause any adverse effects on pregnancy, fetal development, or offspring behavior. One maternal immunization fully protects dams against ZIKV infection and in utero transmission. Although neutralizing antibody alone is sufficient to prevent in utero transmission, a higher neutralizing titer is required to protect pregnant mice against in utero transmission than that required to protect non-pregnant mice against viral infection. The immunized dams transfer maternal antibodies to pups, which protect neonates against ZIKV infection. Notably, pregnancy weakens maternal T cell response to 3ʹUTR-∆10-LAV vaccination. Our results suggest that, besides vaccinating non-pregnant individuals, 3ʹUTR-∆10-LAV may also be considered for maternal vaccination. |
format | Online Article Text |
id | pubmed-6908683 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69086832019-12-16 Maternal vaccination and protective immunity against Zika virus vertical transmission Shan, Chao Xie, Xuping Luo, Huanle Muruato, Antonio E. Liu, Yang Wakamiya, Maki La, Jun-Ho Chung, Jin Mo Weaver, Scott C. Wang, Tian Shi, Pei-Yong Nat Commun Article An important goal of the Zika virus (ZIKV) vaccine is to prevent a congenital syndrome in fetuses of pregnant women, but studies directly evaluating maternal vaccination for ZIKV are lacking. Here we report maternal vaccination using a live-attenuated ZIKV vaccine (3ʹUTR-∆10-LAV) in a pregnant mouse model. Maternal immunization with 3ʹUTR-∆10-LAV does not cause any adverse effects on pregnancy, fetal development, or offspring behavior. One maternal immunization fully protects dams against ZIKV infection and in utero transmission. Although neutralizing antibody alone is sufficient to prevent in utero transmission, a higher neutralizing titer is required to protect pregnant mice against in utero transmission than that required to protect non-pregnant mice against viral infection. The immunized dams transfer maternal antibodies to pups, which protect neonates against ZIKV infection. Notably, pregnancy weakens maternal T cell response to 3ʹUTR-∆10-LAV vaccination. Our results suggest that, besides vaccinating non-pregnant individuals, 3ʹUTR-∆10-LAV may also be considered for maternal vaccination. Nature Publishing Group UK 2019-12-12 /pmc/articles/PMC6908683/ /pubmed/31831806 http://dx.doi.org/10.1038/s41467-019-13589-1 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Shan, Chao Xie, Xuping Luo, Huanle Muruato, Antonio E. Liu, Yang Wakamiya, Maki La, Jun-Ho Chung, Jin Mo Weaver, Scott C. Wang, Tian Shi, Pei-Yong Maternal vaccination and protective immunity against Zika virus vertical transmission |
title | Maternal vaccination and protective immunity against Zika virus vertical transmission |
title_full | Maternal vaccination and protective immunity against Zika virus vertical transmission |
title_fullStr | Maternal vaccination and protective immunity against Zika virus vertical transmission |
title_full_unstemmed | Maternal vaccination and protective immunity against Zika virus vertical transmission |
title_short | Maternal vaccination and protective immunity against Zika virus vertical transmission |
title_sort | maternal vaccination and protective immunity against zika virus vertical transmission |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6908683/ https://www.ncbi.nlm.nih.gov/pubmed/31831806 http://dx.doi.org/10.1038/s41467-019-13589-1 |
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