Cystic fibrosis microbiology: advances in antimicrobial therapy

Much of the improvement in the survival of individuals with cystic fibrosis (CF) is due to advancements in antimicrobial treatments. New aerosolized antibiotic formulations have recently been introduced (such as inhaled aztreonam), and others are in development (inhaled levofloxacin and liposomal a...

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Main Authors: Waters, Valerie, Smyth, Alan R.
Format: Article
Published: Elsevier 2015
Online Access:https://eprints.nottingham.ac.uk/31681/
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author Waters, Valerie
Smyth, Alan R.
author_facet Waters, Valerie
Smyth, Alan R.
author_sort Waters, Valerie
building Nottingham Research Data Repository
collection Online Access
description Much of the improvement in the survival of individuals with cystic fibrosis (CF) is due to advancements in antimicrobial treatments. New aerosolized antibiotic formulations have recently been introduced (such as inhaled aztreonam), and others are in development (inhaled levofloxacin and liposomal amikacin). Licensed dry powder formulations include tobramycin inhalation powder and dry powder colistimethate (available in Europe). Although inhaled antibiotics have the advantage of being able to deliver high intrapulmonary concentrations of drug, antimicrobial resistance can still develop and is a concern in CF. Antimicrobial resistance might be mitigated by using non-antibiotic treatments, antibiotic adjuvants, which have activity against bacteria. Examples include agents such as gallium, antimicrobial peptides and anti-biofilm compounds such as alginate oligosaccharides (OligoG) and garlic. Vaccination strategies and antibody therapy (IgY) against Pseudomonas aeruginosa have also been attempted to prevent initial infection with this organism in CF. Although aggressive and long-term use of antibiotics has been crucial in slowing lung function decline and improving survival in people with CF, it has added a significant burden of care and associated toxicities in these individuals. Careful surveillance and the use of preventative strategies for antibiotic related toxicity (such as nephrotoxicity and ototoxicity) are essential. Continued development of effective antimicrobial agents that can function in the conditions encountered in the CF lung, such as against bacterial biofilm growth and under anaerobic conditions, is needed.
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spelling nottingham-316812020-05-04T20:07:41Z https://eprints.nottingham.ac.uk/31681/ Cystic fibrosis microbiology: advances in antimicrobial therapy Waters, Valerie Smyth, Alan R. Much of the improvement in the survival of individuals with cystic fibrosis (CF) is due to advancements in antimicrobial treatments. New aerosolized antibiotic formulations have recently been introduced (such as inhaled aztreonam), and others are in development (inhaled levofloxacin and liposomal amikacin). Licensed dry powder formulations include tobramycin inhalation powder and dry powder colistimethate (available in Europe). Although inhaled antibiotics have the advantage of being able to deliver high intrapulmonary concentrations of drug, antimicrobial resistance can still develop and is a concern in CF. Antimicrobial resistance might be mitigated by using non-antibiotic treatments, antibiotic adjuvants, which have activity against bacteria. Examples include agents such as gallium, antimicrobial peptides and anti-biofilm compounds such as alginate oligosaccharides (OligoG) and garlic. Vaccination strategies and antibody therapy (IgY) against Pseudomonas aeruginosa have also been attempted to prevent initial infection with this organism in CF. Although aggressive and long-term use of antibiotics has been crucial in slowing lung function decline and improving survival in people with CF, it has added a significant burden of care and associated toxicities in these individuals. Careful surveillance and the use of preventative strategies for antibiotic related toxicity (such as nephrotoxicity and ototoxicity) are essential. Continued development of effective antimicrobial agents that can function in the conditions encountered in the CF lung, such as against bacterial biofilm growth and under anaerobic conditions, is needed. Elsevier 2015-09 Article PeerReviewed Waters, Valerie and Smyth, Alan R. (2015) Cystic fibrosis microbiology: advances in antimicrobial therapy. Journal of Cystic Fibrosis, 14 (5). pp. 551-560. ISSN 1873-5010 http://www.sciencedirect.com/science/article/pii/S1569199315000430 doi:10.1016/j.jcf.2015.02.005 doi:10.1016/j.jcf.2015.02.005
spellingShingle Waters, Valerie
Smyth, Alan R.
Cystic fibrosis microbiology: advances in antimicrobial therapy
title Cystic fibrosis microbiology: advances in antimicrobial therapy
title_full Cystic fibrosis microbiology: advances in antimicrobial therapy
title_fullStr Cystic fibrosis microbiology: advances in antimicrobial therapy
title_full_unstemmed Cystic fibrosis microbiology: advances in antimicrobial therapy
title_short Cystic fibrosis microbiology: advances in antimicrobial therapy
title_sort cystic fibrosis microbiology: advances in antimicrobial therapy
url https://eprints.nottingham.ac.uk/31681/
https://eprints.nottingham.ac.uk/31681/
https://eprints.nottingham.ac.uk/31681/