The hygiene hypothesis postulates that exposure to microbes early in life provides critical stimuli that drive immune system maturation away from the development of allergic susceptibility. The objective of this competing renewal is to investigate three immunologic pathways that appear to protect against asthma, to determine whether these pathways provide a mechanistic basis for the hygiene hypothesis, and to determine how asthma susceptibility genes may interact with environmental influences to protect against asthma.
The specific aims of the project are to: (1) determine the relation between the capacity to produce IFN-gamma in infancy and the risk for the subsequent development of asthma, and to identify any influence of microbial exposure or single nucleofide polymorphisms (SNPs) in pattern recognition receptors on that development; (2) establish the influence of IL-10 production in early life on the ratio of allergen specific IgG4/IgE and the subsequent development of asthma, and to determine the influence of the innate immunity genes TLR4 and CD14 on IL-10 production; (3) establish the biologic basis for the decreased prevalence of asthma associated with a particular SNP in TLR4; and (4) assess the influence, separately and combined, of TLR SNPs and household microbial exposure on peripheral blood monocyte expression of TLRs in early life. The project builds on the successful, on-going Infant Immune Study, which is following a birth cohort to 8 years of age. The competing renewal will enroll the last third of the population of infants required for adequate statistical power, will newly assess early microbial exposures, allergen specific IgG4, and TLR expression, and will follow already enrolled subjects to age 8. Blood is obtained for DNA and immunologic assessments (cytokine production, total IgE, allergenspecific IgE and IgG4) six times in the first 5 years of life; blood is also drawn on parents. Skin prick tests are administered to parents and, at age 5, to the children. Respiratory questionnaires are obtained frequently to determine onset and recurrence of asthma symptoms, and medical record reviews conducted to identify diagnosis of asthma and other respiratory conditions. Dust samples are obtained from the home in early infancy to assess exposure to endotoxin, and Gram-negative, Gram-positive and total bacteria. This project integrates epidemiologic, immunologic, genetic, and molecular approaches to study, in a comprehensive manner, how environmental factors and genetic susceptibility interact to alter the maturation of the immune system and subsequent risk of asthma. An understanding of these processes is critical to elucidating the pathogenesis of asthma, and the development of effective strategies for the primary prevention of asthma.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Project (R01)
Project #
2R01AI042268-06
Application #
6576747
Study Section
Special Emphasis Panel (ZRG1-EDC-3 (01))
Program Officer
Hackett, Charles J
Project Start
1998-01-01
Project End
2007-12-31
Budget Start
2003-01-01
Budget End
2003-12-31
Support Year
6
Fiscal Year
2003
Total Cost
$543,346
Indirect Cost
Name
University of Arizona
Department
Pediatrics
Type
Schools of Medicine
DUNS #
806345617
City
Tucson
State
AZ
Country
United States
Zip Code
85721
Rothers, Janet; Stern, Debra A; Lohman, I Carla et al. (2018) Maternal Cytokine Profiles during Pregnancy Predict Asthma in Children of Mothers without Asthma. Am J Respir Cell Mol Biol 59:592-600
DeVries, Avery; Wlasiuk, Gabriela; Miller, Susan J et al. (2017) Epigenome-wide analysis links SMAD3 methylation at birth to asthma in children of asthmatic mothers. J Allergy Clin Immunol 140:534-542
Xu, Haili; Radabaugh, Timothy; Lu, Zhenqiang et al. (2016) Exploration of early-life candidate biomarkers for childhood asthma using antibody arrays. Pediatr Allergy Immunol 27:696-701
Oren, E; Rothers, J; Stern, D A et al. (2015) Cough during infancy and subsequent childhood asthma. Clin Exp Allergy 45:1439-46
Halonen, Marilyn; Lohman, I Carla; Stern, Debra A et al. (2013) Perinatal tumor necrosis factor-? production, influenced by maternal pregnancy weight gain, predicts childhood asthma. Am J Respir Crit Care Med 188:35-41
Thompson, Emma E; Myers, Rachel A; Du, Gaixin et al. (2013) Maternal microchimerism protects against the development of asthma. J Allergy Clin Immunol 132:39-44
Grad, Roni; Morgan, Wayne J (2012) Long-term outcomes of early-onset wheeze and asthma. J Allergy Clin Immunol 130:299-307
Sevgican, Ufuk; Rothers, Janet; Stern, Debra A et al. (2012) Predictors of neonatal production of IFN-? and relation to later wheeze. J Allergy Clin Immunol 129:567-8, 568.e1
Rothers, Janet; Halonen, Marilyn; Stern, Debra A et al. (2011) Adaptive cytokine production in early life differentially predicts total IgE levels and asthma through age 5 years. J Allergy Clin Immunol 128:397-402.e2
Rothers, Janet; Wright, Anne L; Stern, Debra A et al. (2011) Cord blood 25-hydroxyvitamin D levels are associated with aeroallergen sensitization in children from Tucson, Arizona. J Allergy Clin Immunol 128:1093-9.e1-5

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