Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2021:265:157-186.
doi: 10.1007/164_2020_366.

Disease Models: Lung Models for Testing Drugs Against Inflammation and Infection

Affiliations

Disease Models: Lung Models for Testing Drugs Against Inflammation and Infection

Patrick Carius et al. Handb Exp Pharmacol. 2021.

Abstract

Lung diseases have increasingly attracted interest in the past years. The all-known fear of failing treatments against severe pulmonary infections and plans of the pharmaceutical industry to limit research on anti-infectives to a minimum due to cost reasons makes infections of the lung nowadays a "hot topic." Inhalable antibiotics show promising efficacy while limiting adverse systemic effects to a minimum. Moreover, in times of increased life expectancy in developed countries, the treatment of chronic maladies implicating inflammatory diseases, like bronchial asthma or chronic obstructive pulmonary disease, becomes more and more exigent and still lacks proper treatment.In this chapter, we address in vitro models as well as necessary in vivo models to help develop new drugs for the treatment of various severe pulmonary diseases with a strong focus on infectious diseases. By first presenting the essential hands-on techniques for the setup of in vitro models, we intend to combine these with already successful and interesting model approaches to serve as some guideline for the development of future models. The overall goal is to maximize time and cost-efficacy and to minimize attrition as well as animal trials when developing novel anti-infective therapeutics.

Keywords: Air-blood barrier; Air-liquid interface (ALI); Biofilm; Cystic fibrosis; Deposition; Mycobacterium tuberculosis; Pseudomonas aeruginosa; Transepithelial electrical resistance (TEER); Tuberculosis.

PubMed Disclaimer

References

    1. Adamson J, Haswell LE, Phillips G, Gaça MD (2011) In vitro models of chronic obstructive pulmonary disease (COPD). In: Martn-Loeches I (ed) Bronchitis. InTech, London
    1. Ahluwalia N, Shea BS, Tager AM (2014) New therapeutic targets in idiopathic pulmonary fibrosis. Aiming to rein in runaway wound-healing responses. Am J Respir Crit Care Med 190:867–878. https://doi.org/10.1164/rccm.201403-0509PP - DOI - PubMed - PMC
    1. Alhede M, Bjarnsholt T, Givskov M, Alhede M (2014) Pseudomonas aeruginosa biofilms: mechanisms of immune evasion. Adv Appl Microbiol 86:1–40. https://doi.org/10.1016/B978-0-12-800262-9.00001-9 - DOI - PubMed
    1. Alnimr AM (2015) Dormancy models for Mycobacterium tuberculosis: a minireview. Braz J Microbiol 46:641–647. https://doi.org/10.1590/S1517-838246320140507 - DOI - PubMed - PMC
    1. Anderson GG, Moreau-Marquis S, Stanton BA, O’Toole GA (2008) In vitro analysis of tobramycin-treated Pseudomonas aeruginosa biofilms on cystic fibrosis-derived airway epithelial cells. Infect Immun 76:1423–1433. https://doi.org/10.1128/IAI.01373-07 - DOI - PubMed - PMC

Substances

LinkOut - more resources