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Inhaled protein/peptide-based therapies for respiratory disease

Asthma, chronic obstructive pulmonary disease (COPD), and cystic fibrosis (CF) are all chronic pulmonary diseases, albeit with different etiologies, that are characterized by airflow limitation, chronic inflammation, and abnormal mucus production/rheology. Small synthetic molecule-based therapies ar...

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Detalles Bibliográficos
Autores principales: Fellner, Robert C., Terryah, Shawn T., Tarran, Robert
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4839019/
https://www.ncbi.nlm.nih.gov/pubmed/27098663
http://dx.doi.org/10.1186/s40348-016-0044-8
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author Fellner, Robert C.
Terryah, Shawn T.
Tarran, Robert
author_facet Fellner, Robert C.
Terryah, Shawn T.
Tarran, Robert
author_sort Fellner, Robert C.
collection PubMed
description Asthma, chronic obstructive pulmonary disease (COPD), and cystic fibrosis (CF) are all chronic pulmonary diseases, albeit with different etiologies, that are characterized by airflow limitation, chronic inflammation, and abnormal mucus production/rheology. Small synthetic molecule-based therapies are commonly prescribed for all three diseases. However, there has been increased interest in “biologicals” to treat these diseases. Biologicals typically constitute protein- or peptide-based therapies and are often more potent than small molecule-based drugs. In this review, we shall describe the pros and cons of several different biological-based therapies for respiratory disease, including dornase alfa, a recombinant DNAase that reduces mucus viscosity and short palate lung and nasal epithelial clone 1 (SPLUNC1)-derived peptides that treat Na(+) hyperabsorption and rebalance CF airway surface liquid homeostasis.
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spelling pubmed-48390192016-05-16 Inhaled protein/peptide-based therapies for respiratory disease Fellner, Robert C. Terryah, Shawn T. Tarran, Robert Mol Cell Pediatr Review Asthma, chronic obstructive pulmonary disease (COPD), and cystic fibrosis (CF) are all chronic pulmonary diseases, albeit with different etiologies, that are characterized by airflow limitation, chronic inflammation, and abnormal mucus production/rheology. Small synthetic molecule-based therapies are commonly prescribed for all three diseases. However, there has been increased interest in “biologicals” to treat these diseases. Biologicals typically constitute protein- or peptide-based therapies and are often more potent than small molecule-based drugs. In this review, we shall describe the pros and cons of several different biological-based therapies for respiratory disease, including dornase alfa, a recombinant DNAase that reduces mucus viscosity and short palate lung and nasal epithelial clone 1 (SPLUNC1)-derived peptides that treat Na(+) hyperabsorption and rebalance CF airway surface liquid homeostasis. Springer Berlin Heidelberg 2016-04-20 /pmc/articles/PMC4839019/ /pubmed/27098663 http://dx.doi.org/10.1186/s40348-016-0044-8 Text en © Fellner et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Review
Fellner, Robert C.
Terryah, Shawn T.
Tarran, Robert
Inhaled protein/peptide-based therapies for respiratory disease
title Inhaled protein/peptide-based therapies for respiratory disease
title_full Inhaled protein/peptide-based therapies for respiratory disease
title_fullStr Inhaled protein/peptide-based therapies for respiratory disease
title_full_unstemmed Inhaled protein/peptide-based therapies for respiratory disease
title_short Inhaled protein/peptide-based therapies for respiratory disease
title_sort inhaled protein/peptide-based therapies for respiratory disease
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4839019/
https://www.ncbi.nlm.nih.gov/pubmed/27098663
http://dx.doi.org/10.1186/s40348-016-0044-8
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