Literature DB >> 17467552

Inflammation and anti-inflammatory therapies for cystic fibrosis.

James F Chmiel1, Michael W Konstan.   

Abstract

Cystic fibrosis lung disease is characterized by a self-propagating cycle of obstruction, infection, and inflammation. The inflammatory response, which accounts for the majority of the morbidity and mortality of the disease, begins early in life, becomes persistent, and is excessive relative to the bacterial burden. Therapies aimed at decreasing the inflammatory response represent a relatively new strategy for treatment. This article reviews the current state of the art of anti-inflammatory therapy in cystic fibrosis and introduces clinical trials that are underway.

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Year:  2007        PMID: 17467552     DOI: 10.1016/j.ccm.2007.02.002

Source DB:  PubMed          Journal:  Clin Chest Med        ISSN: 0272-5231            Impact factor:   2.878


  34 in total

Review 1.  Unmet needs in cystic fibrosis: the next steps in improving outcomes.

Authors:  Natalie E West; Patrick A Flume
Journal:  Expert Rev Respir Med       Date:  2018-06-19       Impact factor: 3.772

2.  A randomized double blind, placebo controlled phase 2 trial of BIIL 284 BS (an LTB4 receptor antagonist) for the treatment of lung disease in children and adults with cystic fibrosis.

Authors:  M W Konstan; G Döring; S L Heltshe; L C Lands; K A Hilliard; P Koker; S Bhattacharya; A Staab; A Hamilton
Journal:  J Cyst Fibros       Date:  2014-01-17       Impact factor: 5.482

3.  The I-neb Adaptive Aerosol Delivery System enhances delivery of alpha1-antitrypsin with controlled inhalation.

Authors:  David E Geller; Kenneth C Kesser
Journal:  J Aerosol Med Pulm Drug Deliv       Date:  2010-04       Impact factor: 2.849

4.  Quantitative microscopy in murine models of lung inflammation.

Authors:  Joseph Soltzberg; Sarah Frischmann; Christiaan van Heeckeren; Nicole Brown; Arnold Caplan; Tracey L Bonfield
Journal:  Anal Quant Cytol Histol       Date:  2011-10       Impact factor: 0.302

Review 5.  Cystic fibrosis therapeutics: the road ahead.

Authors:  Lucas R Hoffman; Bonnie W Ramsey
Journal:  Chest       Date:  2013-01       Impact factor: 9.410

6.  Regulatory role of β-arrestin-2 in cholesterol processing in cystic fibrosis epithelial cells.

Authors:  Mary E Manson; Deborah A Corey; Ilya Bederman; James D Burgess; Thomas J Kelley
Journal:  J Lipid Res       Date:  2012-04-22       Impact factor: 5.922

7.  CFTR-deficient pigs display peripheral nervous system defects at birth.

Authors:  Leah R Reznikov; Qian Dong; Jeng-Haur Chen; Thomas O Moninger; Jung Min Park; Yuzhou Zhang; Jianyang Du; Michael S Hildebrand; Richard J H Smith; Christoph O Randak; David A Stoltz; Michael J Welsh
Journal:  Proc Natl Acad Sci U S A       Date:  2013-02-04       Impact factor: 11.205

8.  HE3286, an oral synthetic steroid, treats lung inflammation in mice without immune suppression.

Authors:  Douglas Conrad; Angela Wang; Raymond Pieters; Ferdinando Nicoletti; Katia Mangano; Anna M van Heeckeren; Steven K White; James M Frincke; Christopher L Reading; Dwight Stickney; Dominick L Auci
Journal:  J Inflamm (Lond)       Date:  2010-10-30       Impact factor: 4.981

9.  Stabilization of lung function and clinical symptoms in a patient with cystic fibrosis (CF) after institution of infliximab: a monoclonal antibody that binds tumor necrosis factor alpha.

Authors:  Brian Casserly; Walter Donat
Journal:  Lung       Date:  2009-02-27       Impact factor: 2.584

10.  Absence of the cystic fibrosis transmembrane regulator (Cftr) from myeloid-derived cells slows resolution of inflammation and infection.

Authors:  T L Bonfield; C A Hodges; C U Cotton; M L Drumm
Journal:  J Leukoc Biol       Date:  2012-08-02       Impact factor: 4.962

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