Fig. 1 Compromised hBD-2 function in the CF lung promotes chronic

pulmonary infection by the opportunistic pathogen P. aeruginosa Acknowledgments STI571 supplier This project was funded by an Undergraduate Student Research Award from the Natural Sciences and Engineering Research Council of Canada. Dalcin is the guarantor for this article, and takes responsibility for the integrity of the work as a whole. Conflict of interest Dalcin and Dr Ulanova declare no conflict of interest. Compliance with ethics The analysis in this article is based on previously conducted studies, and does not involve any new studies of human or animal subjects performed by any of the authors. Open Access This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited. References 1. Bals R, Weiner DJ, Wilson JM. The innate immune system in cystic fibrosis lung disease. J Clin Invest. 1999;103:303–7.PubMedCentralPubMedCrossRef 2. Dodge JA, Morison S, Lewis PA, et al. Incidence, population, and GSI-IX mw survival of cystic fibrosis in the UK, 1968–95. Arch Dis Child. 1997;77:493–6.PubMedCentralPubMedCrossRef 3. Rommens JM, Lannuzzi MC, Kerem B, et al. Identification

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