作者
David A Stoltz, 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 IV, 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 Jr, Joseph Zabner, Michael J Welsh
发表日期
2010/4/28
期刊
Science translational medicine
卷号
2
期号
29
页码范围
29ra31-29ra31
出版商
American Association for the Advancement of Science
简介
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 …
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