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Mechanistic research holds promise for bacterial vaccines and phage therapies for Pseudomonas aeruginosa
Vaccines for Pseudomonas aeruginosa have been of longstanding interest to immunologists, bacteriologists, and clinicians, due to the widespread prevalence of hospital-acquired infection. As P. aeruginosa becomes increasingly antibiotic resistant, there is a dire need for novel treatments and prevent...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6431001/ https://www.ncbi.nlm.nih.gov/pubmed/30936684 http://dx.doi.org/10.2147/DDDT.S189847 |
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author | Hoggarth, Austin Weaver, Andrew Pu, Qinqin Huang, Ting Schettler, Jacob Chen, Feng Yuan, Xiefang Wu, Min |
author_facet | Hoggarth, Austin Weaver, Andrew Pu, Qinqin Huang, Ting Schettler, Jacob Chen, Feng Yuan, Xiefang Wu, Min |
author_sort | Hoggarth, Austin |
collection | PubMed |
description | Vaccines for Pseudomonas aeruginosa have been of longstanding interest to immunologists, bacteriologists, and clinicians, due to the widespread prevalence of hospital-acquired infection. As P. aeruginosa becomes increasingly antibiotic resistant, there is a dire need for novel treatments and preventive vaccines. Despite intense efforts, there currently remains no vaccine on the market to combat this dangerous pathogen. This article summarizes current and past vaccines under development that target various constituents of P. aeruginosa. Targeting lipopolysaccharides and O-antigens have shown some promise in preventing infection. Recombinant flagella and pili that target TLR5 have been utilized to combat P. aeruginosa by blocking its motility and adhesion. The type 3 secretion system components, such as needle-like structure PcrV or exotoxin PopB, are also potential vaccine targets. Outer membrane proteins including OprF and OprI are newer representatives of vaccine candidates. Live attenuated vaccines are a focal point in this review, and are also considered for novel vaccines. In addition, phage therapy is revived as an effective option for treating refractory infections after failure with antibiotic treatment. Many of the aforementioned vaccines act on a single target, thus lacking a broad range of protection. Recent studies have shown that mixtures of vaccines and combination approaches may significantly augment immunogenicity, thereby increasing their preventive and therapeutic potential. |
format | Online Article Text |
id | pubmed-6431001 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-64310012019-04-01 Mechanistic research holds promise for bacterial vaccines and phage therapies for Pseudomonas aeruginosa Hoggarth, Austin Weaver, Andrew Pu, Qinqin Huang, Ting Schettler, Jacob Chen, Feng Yuan, Xiefang Wu, Min Drug Des Devel Ther Review Vaccines for Pseudomonas aeruginosa have been of longstanding interest to immunologists, bacteriologists, and clinicians, due to the widespread prevalence of hospital-acquired infection. As P. aeruginosa becomes increasingly antibiotic resistant, there is a dire need for novel treatments and preventive vaccines. Despite intense efforts, there currently remains no vaccine on the market to combat this dangerous pathogen. This article summarizes current and past vaccines under development that target various constituents of P. aeruginosa. Targeting lipopolysaccharides and O-antigens have shown some promise in preventing infection. Recombinant flagella and pili that target TLR5 have been utilized to combat P. aeruginosa by blocking its motility and adhesion. The type 3 secretion system components, such as needle-like structure PcrV or exotoxin PopB, are also potential vaccine targets. Outer membrane proteins including OprF and OprI are newer representatives of vaccine candidates. Live attenuated vaccines are a focal point in this review, and are also considered for novel vaccines. In addition, phage therapy is revived as an effective option for treating refractory infections after failure with antibiotic treatment. Many of the aforementioned vaccines act on a single target, thus lacking a broad range of protection. Recent studies have shown that mixtures of vaccines and combination approaches may significantly augment immunogenicity, thereby increasing their preventive and therapeutic potential. Dove Medical Press 2019-03-20 /pmc/articles/PMC6431001/ /pubmed/30936684 http://dx.doi.org/10.2147/DDDT.S189847 Text en © 2019 Hoggarth et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Review Hoggarth, Austin Weaver, Andrew Pu, Qinqin Huang, Ting Schettler, Jacob Chen, Feng Yuan, Xiefang Wu, Min Mechanistic research holds promise for bacterial vaccines and phage therapies for Pseudomonas aeruginosa |
title | Mechanistic research holds promise for bacterial vaccines and phage therapies for Pseudomonas aeruginosa |
title_full | Mechanistic research holds promise for bacterial vaccines and phage therapies for Pseudomonas aeruginosa |
title_fullStr | Mechanistic research holds promise for bacterial vaccines and phage therapies for Pseudomonas aeruginosa |
title_full_unstemmed | Mechanistic research holds promise for bacterial vaccines and phage therapies for Pseudomonas aeruginosa |
title_short | Mechanistic research holds promise for bacterial vaccines and phage therapies for Pseudomonas aeruginosa |
title_sort | mechanistic research holds promise for bacterial vaccines and phage therapies for pseudomonas aeruginosa |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6431001/ https://www.ncbi.nlm.nih.gov/pubmed/30936684 http://dx.doi.org/10.2147/DDDT.S189847 |
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