Broad and Effective Protection against <named-content content-type="genus-species">Staphylococcus aureus</named-content> Is Elicited by a Multivalent Vaccine Formulated with Novel Antigens
ABSTRACT The demand for a prophylactic vaccine against methicillin-resistant Staphylococcus aureus (MRSA) has motivated numerous dedicated research groups to design and develop such a vaccine. In this study, we have developed a multivalent vaccine, Sta-V5, composed of five conserved antigens involve...
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American Society for Microbiology
2019
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oai:doaj.org-article:2c8355ae80914d0ebaedda23bd961a802021-11-15T15:27:32ZBroad and Effective Protection against <named-content content-type="genus-species">Staphylococcus aureus</named-content> Is Elicited by a Multivalent Vaccine Formulated with Novel Antigens10.1128/mSphere.00362-192379-5042https://doaj.org/article/2c8355ae80914d0ebaedda23bd961a802019-10-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mSphere.00362-19https://doaj.org/toc/2379-5042ABSTRACT The demand for a prophylactic vaccine against methicillin-resistant Staphylococcus aureus (MRSA) has motivated numerous dedicated research groups to design and develop such a vaccine. In this study, we have developed a multivalent vaccine, Sta-V5, composed of five conserved antigens involved in three important virulence mechanisms. This prototype vaccine conferred up to 100% protection against multiple epidemiologically relevant S. aureus isolates in five different murine disease models. The vaccine not only elicits functional antibodies that mediate opsonophagocytic killing of S. aureus but also mounts robust antigen-specific T-cell responses. In addition, our data implied that γδ T cells contribute to the protection induced by Sta-V5 in a murine skin infection model. IMPORTANCE Staphylococcus aureus infections, especially MRSA infections, are becoming a major global health issue and are resulting in mortality rates that are increasing every year. However, an effective vaccine is lacking due to the complexity of the infection process of S. aureus. In this study, we found that the addition of two novel protein components to three well-studied vaccine candidates significantly improved the efficacy of the combined vaccine. Furthermore, the five-component vaccine not only elicits a robust antibody response but also induces cytokine secretion by T cells, making it a promising vaccine candidate to fill the void.Jian DengXiaolei WangBao-Zhong ZhangPeng GaoQiubin LinRichard Yi-Tsun KaoKenth GustafssonKwok-Yung YuenJian-Dong HuangAmerican Society for Microbiologyarticleγδ T cellMRSAmultivalent vaccineMicrobiologyQR1-502ENmSphere, Vol 4, Iss 5 (2019) |
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γδ T cell MRSA multivalent vaccine Microbiology QR1-502 |
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γδ T cell MRSA multivalent vaccine Microbiology QR1-502 Jian Deng Xiaolei Wang Bao-Zhong Zhang Peng Gao Qiubin Lin Richard Yi-Tsun Kao Kenth Gustafsson Kwok-Yung Yuen Jian-Dong Huang Broad and Effective Protection against <named-content content-type="genus-species">Staphylococcus aureus</named-content> Is Elicited by a Multivalent Vaccine Formulated with Novel Antigens |
description |
ABSTRACT The demand for a prophylactic vaccine against methicillin-resistant Staphylococcus aureus (MRSA) has motivated numerous dedicated research groups to design and develop such a vaccine. In this study, we have developed a multivalent vaccine, Sta-V5, composed of five conserved antigens involved in three important virulence mechanisms. This prototype vaccine conferred up to 100% protection against multiple epidemiologically relevant S. aureus isolates in five different murine disease models. The vaccine not only elicits functional antibodies that mediate opsonophagocytic killing of S. aureus but also mounts robust antigen-specific T-cell responses. In addition, our data implied that γδ T cells contribute to the protection induced by Sta-V5 in a murine skin infection model. IMPORTANCE Staphylococcus aureus infections, especially MRSA infections, are becoming a major global health issue and are resulting in mortality rates that are increasing every year. However, an effective vaccine is lacking due to the complexity of the infection process of S. aureus. In this study, we found that the addition of two novel protein components to three well-studied vaccine candidates significantly improved the efficacy of the combined vaccine. Furthermore, the five-component vaccine not only elicits a robust antibody response but also induces cytokine secretion by T cells, making it a promising vaccine candidate to fill the void. |
format |
article |
author |
Jian Deng Xiaolei Wang Bao-Zhong Zhang Peng Gao Qiubin Lin Richard Yi-Tsun Kao Kenth Gustafsson Kwok-Yung Yuen Jian-Dong Huang |
author_facet |
Jian Deng Xiaolei Wang Bao-Zhong Zhang Peng Gao Qiubin Lin Richard Yi-Tsun Kao Kenth Gustafsson Kwok-Yung Yuen Jian-Dong Huang |
author_sort |
Jian Deng |
title |
Broad and Effective Protection against <named-content content-type="genus-species">Staphylococcus aureus</named-content> Is Elicited by a Multivalent Vaccine Formulated with Novel Antigens |
title_short |
Broad and Effective Protection against <named-content content-type="genus-species">Staphylococcus aureus</named-content> Is Elicited by a Multivalent Vaccine Formulated with Novel Antigens |
title_full |
Broad and Effective Protection against <named-content content-type="genus-species">Staphylococcus aureus</named-content> Is Elicited by a Multivalent Vaccine Formulated with Novel Antigens |
title_fullStr |
Broad and Effective Protection against <named-content content-type="genus-species">Staphylococcus aureus</named-content> Is Elicited by a Multivalent Vaccine Formulated with Novel Antigens |
title_full_unstemmed |
Broad and Effective Protection against <named-content content-type="genus-species">Staphylococcus aureus</named-content> Is Elicited by a Multivalent Vaccine Formulated with Novel Antigens |
title_sort |
broad and effective protection against <named-content content-type="genus-species">staphylococcus aureus</named-content> is elicited by a multivalent vaccine formulated with novel antigens |
publisher |
American Society for Microbiology |
publishDate |
2019 |
url |
https://doaj.org/article/2c8355ae80914d0ebaedda23bd961a80 |
work_keys_str_mv |
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