Literature DB >> 19393104

Cystic fibrosis: pathogenesis and future treatment strategies.

Felix A Ratjen1.   

Abstract

Since the detection of the underlying gene defect, our knowledge of how the genetic mutations in cystic fibrosis cause lung disease has increased substantially, but we still lack a complete understanding of some of the pieces in the puzzle. Nevertheless, the information gained has led to new therapeutic approaches that address key factors of cystic fibrosis pathophysiology. Past therapeutic successes were largely based on targeting the consequences of the cystic fibrosis transmembrane regulator dysfunction, such as phlegm retention, infection, and inflammation, but new therapies may be able to address the underlying abnormality rather than its downstream effects. The efficacy of these treatments still needs to be established, but early studies look promising for several compounds. This review summarizes our current understanding of the pathophysiology and treatment of cystic fibrosis lung disease.

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Year:  2009        PMID: 19393104     DOI: 10.4187/aarc0427

Source DB:  PubMed          Journal:  Respir Care        ISSN: 0020-1324            Impact factor:   2.258


  38 in total

1.  Vaccine strategies against cystic fibrosis pathogens.

Authors:  Vincent Le Moigne; Jean-Louis Gaillard; Jean-Louis Herrmann
Journal:  Hum Vaccin Immunother       Date:  2016-03-03       Impact factor: 3.452

2.  Antibiofilm Efficacy of Nitric Oxide-Releasing Alginates against Cystic Fibrosis Bacterial Pathogens.

Authors:  Mona Jasmine R Ahonen; Jamie M Dorrier; Mark H Schoenfisch
Journal:  ACS Infect Dis       Date:  2019-06-11       Impact factor: 5.084

3.  β-Lactam Combinations That Exhibit Synergy against Mycobacteroides abscessus Clinical Isolates.

Authors:  Elizabeth Story-Roller; Christos Galanis; Gyanu Lamichhane
Journal:  Antimicrob Agents Chemother       Date:  2021-03-18       Impact factor: 5.191

4.  Triggering receptor expressed on myeloid cells-1 as a new therapeutic target during inflammatory diseases.

Authors:  Marc Derive; Frédéric Massin; Sébastien Gibot
Journal:  Self Nonself       Date:  2010-07-02

5.  A French multicentric study and review of pulmonary Nocardia spp. in cystic fibrosis patients.

Authors:  Verónica Rodriguez-Nava; Stéphane Durupt; Sandra Chyderiotis; Anne-Marie Freydière; Judith Karsenty; Michèle de Montclos; Philippe Reix; Isabelle Durieu; Raphaele Nove-Josserand; Raphael Chiron; François Bremont; Laurent Têtu; Marlène Murris; Dominique Terru; Sylvain Godreuil; Emmanuelle Bergeron; Jean Freney; Patrick Boiron; François Vandenesch; Hélène Marchandin; Christine Segonds; Anne Doléans-Jordheim
Journal:  Med Microbiol Immunol       Date:  2014-10-26       Impact factor: 3.402

Review 6.  Synthetic Biology Approaches to Engineer Probiotics and Members of the Human Microbiota for Biomedical Applications.

Authors:  Josef R Bober; Chase L Beisel; Nikhil U Nair
Journal:  Annu Rev Biomed Eng       Date:  2018-03-12       Impact factor: 9.590

7.  A template for mutational data analysis of the CFTR gene.

Authors:  Giampiero Ferraguti; Silvia Pierandrei; Sabina Maria Bruno; Fabrizio Ceci; Roberto Strom; Marco Lucarelli
Journal:  Clin Chem Lab Med       Date:  2011-05-31       Impact factor: 3.694

8.  Down-regulation of cytokine-induced interleukin-8 requires inhibition of p38 mitogen-activated protein kinase (MAPK) via MAPK phosphatase 1-dependent and -independent mechanisms.

Authors:  Nurlan Dauletbaev; Daniel Eklove; Nadir Mawji; Michele Iskandar; Sergio Di Marco; Imed-Eddine Gallouzi; Larry C Lands
Journal:  J Biol Chem       Date:  2011-03-15       Impact factor: 5.157

9.  CFTR Modulators for the Treatment of Cystic Fibrosis.

Authors:  Rebecca S Pettit; Chris Fellner
Journal:  P T       Date:  2014-07

10.  Effects of Autogenic Drainage on Sputum Recovery and Pulmonary Function in People with Cystic Fibrosis: A Systematic Review.

Authors:  Kimbly Morgan; Kristin Osterling; Robert Gilbert; Gail Dechman
Journal:  Physiother Can       Date:  2015       Impact factor: 1.037

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