Literature DB >> 20427821

Cystic fibrosis pigs develop lung disease and exhibit defective bacterial eradication at birth.

David A Stoltz1, David K Meyerholz, Alejandro A Pezzulo, Shyam Ramachandran, Mark P Rogan, Greg J Davis, Robert A Hanfland, Chris Wohlford-Lenane, Cassie L Dohrn, Jennifer A Bartlett, George A Nelson, Eugene H Chang, Peter J Taft, Paula S Ludwig, Mira Estin, Emma E Hornick, Janice L Launspach, Melissa Samuel, Tatiana Rokhlina, Philip H Karp, Lynda S Ostedgaard, Aliye Uc, Timothy D Starner, Alexander R Horswill, Kim A Brogden, Randall S Prather, Sandra S Richter, Joel Shilyansky, Paul B McCray, Joseph Zabner, Michael J Welsh.   

Abstract

Lung disease causes most of the morbidity and mortality in cystic fibrosis (CF). Understanding the pathogenesis of this disease has been hindered, however, by the lack of an animal model with characteristic features of CF. To overcome this problem, we recently generated pigs with mutated CFTR genes. We now report that, within months of birth, CF pigs spontaneously developed hallmark features of CF lung disease, including airway inflammation, remodeling, mucus accumulation, and infection. Their lungs contained multiple bacterial species, suggesting that the lungs of CF pigs have a host defense defect against a wide spectrum of bacteria. In humans, the temporal and causal relations between inflammation and infection have remained uncertain. To investigate these processes, we studied newborn pigs. Their lungs showed no inflammation but were less often sterile than controls. Moreover, after introduction of bacteria into their lungs, pigs with CF failed to eradicate bacteria as effectively as wild-type pigs. These results suggest that impaired bacterial elimination is the pathogenic event that initiates a cascade of inflammation and pathology in CF lungs. Our finding that pigs with CF have a host defense defect against bacteria within hours of birth provides an opportunity to further investigate CF pathogenesis and to test therapeutic and preventive strategies that could be deployed before secondary consequences develop.

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Year:  2010        PMID: 20427821      PMCID: PMC2889616          DOI: 10.1126/scitranslmed.3000928

Source DB:  PubMed          Journal:  Sci Transl Med        ISSN: 1946-6234            Impact factor:   17.956


  34 in total

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7.  Acidic Submucosal Gland pH and Elevated Protein Concentration Produce Abnormal Cystic Fibrosis Mucus.

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

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10.  CFTR gene transfer with AAV improves early cystic fibrosis pig phenotypes.

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