The research program seeks to define the role of acute pulmonary infections during early childhood in the pathogenesis of chronic respiratory diseases which may occur in later life. The problem is being approached through interrelated clinical (pediatrics, medical, epidemio/ogic, biostatistical) and basic (microbiological, immunologic, physiologic, pathologic) studies. The research of the component projects will: 1) seek sequelae of bronchiolitis, croup and bronchitis/pneumonia; 2) determine which kinds of pulmonary infections are of prime importance for targeting intervention efforts; 3) attempt to determine the interactive effects of host predisposition, infection and micro-environmental pollution in the causation of respiratory problems; 4) examine airways and lung cell injury by infectious agents, search for contributory host defects and analyze recovery patterns; and 5) use cell cultures and animal models to examine new therapeutic and prophylactic measure for acute bronchiolitis. Populations of children are being studied both prospectively and retrospectively using multiple regression and other statistical approaches to evaluate the impact of defined respiratory infections and other variables on subsequent pulmonary health. Ultrastructural physiologic and metabolic studies of human respiratory epithelial cells (normal and infected) are complemented by similar research on differentiated respiratory cell lines from animals. Synthetic protease inhibitors are being tested for their antiviral properties, and effects of viral antigenic variation on protective immunity will be assessed. Basic studies of the molecular biology are being made of two important respiratory pathogens, Mycoplasma pneumoniae and non-typable Haemophilus influenzae. Together these projects deal with one of the most common childhood problems and one of the more significant debilitating diseases of adults, with the ultimate goal of defining improved methods of diagnosis, treatment and prevention.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Specialized Center (P50)
Project #
5P50HL019171-10
Application #
3106572
Study Section
(SRC)
Project Start
1976-06-30
Project End
1986-11-30
Budget Start
1985-12-01
Budget End
1986-11-30
Support Year
10
Fiscal Year
1986
Total Cost
Indirect Cost
Name
University of North Carolina Chapel Hill
Department
Type
Schools of Medicine
DUNS #
078861598
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599
Gordon, Phillip V; Moats-Staats, Billie M; Stiles, Alan D et al. (2002) Dexamethasone changes the composition of insulin-like growth factor binding proteins in the newborn mouse ileum. J Pediatr Gastroenterol Nutr 35:532-8
Price, Wayne A; Moats-Staats, Billie M; Stiles, Alan D (2002) Pro- and anti-inflammatory cytokines regulate insulin-like growth factor binding protein production by fetal rat lung fibroblasts. Am J Respir Cell Mol Biol 26:283-9
Gordon, P V; Marshall, D D; Stiles, A D et al. (2001) The clinical, morphologic, and molecular changes in the ileum associated with early postnatal dexamethasone administration: from the baby's bowel to the researcher's bench. Mol Genet Metab 72:91-103
Gordon, P V; Price, W A; Stiles, A D et al. (2001) Early postnatal dexamethasone diminishes transforming growth factor alpha localization within the ileal muscularis propria of newborn mice and extremely low-birth-weight infants. Pediatr Dev Pathol 4:532-7
Stiles, A D; Chrysis, D; Jarvis, H W et al. (2001) Programmed cell death in normal fetal rat lung development. Exp Lung Res 27:569-87
Gordon, P V; Price, W A; Stiles, A D (2001) Dexamethasone administration to newborn mice alters mucosal and muscular morphology in the ileum and modulates IGF-I localization. Pediatr Res 49:93-100
Moats-Staats, B M; Jarvis, H W; Brighton, B et al. (2000) Regulation of the rat BB1 RNA during normal rat lung development. Exp Lung Res 26:401-20
Gordon, P; Rutledge, J; Sawin, R et al. (1999) Early postnatal dexamethasone increases the risk of focal small bowel perforation in extremely low birth weight infants. J Perinatol 19:573-7
Price, W A; Moats-Staats, B M; Sekhon, H S et al. (1998) Expression of the insulin-like growth factor system in postpneumonectomy lung growth. Exp Lung Res 24:203-17
Veness-Meehan, K A; Moats-Staats, B M; Maniscalco, W M et al. (1997) Changes in decorin expression with hyperoxic injury to developing rat lung. Pediatr Res 41:464-72

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