Vaccination induces rapid protection against bacterial pneumonia via training alveolar macrophage in mice

Vaccination strategies for rapid protection against multidrug-resistant bacterial infection are very important, especially for hospitalized patients who have high risk of exposure to these bacteria. However, few such vaccination strategies exist due to a shortage of knowledge supporting their rapid...

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Autores principales: Hao Gu, Xi Zeng, Liusheng Peng, Chuanying Xiang, Yangyang Zhou, Xiaomin Zhang, Jixin Zhang, Ning Wang, Gang Guo, Yan Li, Kaiyun Liu, Jiang Gu, Hao Zeng, Yuan Zhuang, Haibo Li, Jinyong Zhang, Weijun Zhang, Quanming Zou, Yun Shi
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Publicado: eLife Sciences Publications Ltd 2021
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spelling oai:doaj.org-article:4dfda56e312643cf88f336477e954a502021-11-30T10:05:54ZVaccination induces rapid protection against bacterial pneumonia via training alveolar macrophage in mice10.7554/eLife.699512050-084Xe69951https://doaj.org/article/4dfda56e312643cf88f336477e954a502021-09-01T00:00:00Zhttps://elifesciences.org/articles/69951https://doaj.org/toc/2050-084XVaccination strategies for rapid protection against multidrug-resistant bacterial infection are very important, especially for hospitalized patients who have high risk of exposure to these bacteria. However, few such vaccination strategies exist due to a shortage of knowledge supporting their rapid effect. Here, we demonstrated that a single intranasal immunization of inactivated whole cell of Acinetobacter baumannii elicits rapid protection against broad A. baumannii-infected pneumonia via training of innate immune response in Rag1-/- mice. Immunization-trained alveolar macrophages (AMs) showed enhanced TNF-α production upon restimulation. Adoptive transfer of immunization-trained AMs into naive mice mediated rapid protection against infection. Elevated TLR4 expression on vaccination-trained AMs contributed to rapid protection. Moreover, immunization-induced rapid protection was also seen in Pseudomonas aeruginosa and Klebsiella pneumoniae pneumonia models, but not in Staphylococcus aureus and Streptococcus pneumoniae model. Our data reveal that a single intranasal immunization induces rapid and efficient protection against certain Gram-negative bacterial pneumonia via training AMs response, which highlights the importance and the possibility of harnessing trained immunity of AMs to design rapid-effecting vaccine.Hao GuXi ZengLiusheng PengChuanying XiangYangyang ZhouXiaomin ZhangJixin ZhangNing WangGang GuoYan LiKaiyun LiuJiang GuHao ZengYuan ZhuangHaibo LiJinyong ZhangWeijun ZhangQuanming ZouYun ShieLife Sciences Publications Ltdarticlemultidrug-resistant bacteriavaccinealveolar macrophageTrained immunityAcinetobacter baumanniirapid effectMedicineRScienceQBiology (General)QH301-705.5ENeLife, Vol 10 (2021)
institution DOAJ
collection DOAJ
language EN
topic multidrug-resistant bacteria
vaccine
alveolar macrophage
Trained immunity
Acinetobacter baumannii
rapid effect
Medicine
R
Science
Q
Biology (General)
QH301-705.5
spellingShingle multidrug-resistant bacteria
vaccine
alveolar macrophage
Trained immunity
Acinetobacter baumannii
rapid effect
Medicine
R
Science
Q
Biology (General)
QH301-705.5
Hao Gu
Xi Zeng
Liusheng Peng
Chuanying Xiang
Yangyang Zhou
Xiaomin Zhang
Jixin Zhang
Ning Wang
Gang Guo
Yan Li
Kaiyun Liu
Jiang Gu
Hao Zeng
Yuan Zhuang
Haibo Li
Jinyong Zhang
Weijun Zhang
Quanming Zou
Yun Shi
Vaccination induces rapid protection against bacterial pneumonia via training alveolar macrophage in mice
description Vaccination strategies for rapid protection against multidrug-resistant bacterial infection are very important, especially for hospitalized patients who have high risk of exposure to these bacteria. However, few such vaccination strategies exist due to a shortage of knowledge supporting their rapid effect. Here, we demonstrated that a single intranasal immunization of inactivated whole cell of Acinetobacter baumannii elicits rapid protection against broad A. baumannii-infected pneumonia via training of innate immune response in Rag1-/- mice. Immunization-trained alveolar macrophages (AMs) showed enhanced TNF-α production upon restimulation. Adoptive transfer of immunization-trained AMs into naive mice mediated rapid protection against infection. Elevated TLR4 expression on vaccination-trained AMs contributed to rapid protection. Moreover, immunization-induced rapid protection was also seen in Pseudomonas aeruginosa and Klebsiella pneumoniae pneumonia models, but not in Staphylococcus aureus and Streptococcus pneumoniae model. Our data reveal that a single intranasal immunization induces rapid and efficient protection against certain Gram-negative bacterial pneumonia via training AMs response, which highlights the importance and the possibility of harnessing trained immunity of AMs to design rapid-effecting vaccine.
format article
author Hao Gu
Xi Zeng
Liusheng Peng
Chuanying Xiang
Yangyang Zhou
Xiaomin Zhang
Jixin Zhang
Ning Wang
Gang Guo
Yan Li
Kaiyun Liu
Jiang Gu
Hao Zeng
Yuan Zhuang
Haibo Li
Jinyong Zhang
Weijun Zhang
Quanming Zou
Yun Shi
author_facet Hao Gu
Xi Zeng
Liusheng Peng
Chuanying Xiang
Yangyang Zhou
Xiaomin Zhang
Jixin Zhang
Ning Wang
Gang Guo
Yan Li
Kaiyun Liu
Jiang Gu
Hao Zeng
Yuan Zhuang
Haibo Li
Jinyong Zhang
Weijun Zhang
Quanming Zou
Yun Shi
author_sort Hao Gu
title Vaccination induces rapid protection against bacterial pneumonia via training alveolar macrophage in mice
title_short Vaccination induces rapid protection against bacterial pneumonia via training alveolar macrophage in mice
title_full Vaccination induces rapid protection against bacterial pneumonia via training alveolar macrophage in mice
title_fullStr Vaccination induces rapid protection against bacterial pneumonia via training alveolar macrophage in mice
title_full_unstemmed Vaccination induces rapid protection against bacterial pneumonia via training alveolar macrophage in mice
title_sort vaccination induces rapid protection against bacterial pneumonia via training alveolar macrophage in mice
publisher eLife Sciences Publications Ltd
publishDate 2021
url https://doaj.org/article/4dfda56e312643cf88f336477e954a50
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