Viral respiratory infections are the major cause of asthma exacerbations. Of the respiratory viruses that precipitate these attacks of asthma, RV is the most frequent. Based upon studies with in vitro models and RV16 inoculation studies of subjects with asthma, evidence shows that RV infection of airway cells generates pro-inflammatory cytokines, i.e., IL-8. The in vivo inoculation of allergic and asthmatic subjects with RV16 generates IL-8, relates to neutrophil recruitment to the airway, and, in some subjects, is associated with increases in airway responsiveness. Finally, there is preliminary evidence that the IFN-gamma generation to RV is reduced in some subjects with asthma, and the dysregulation of this cytokine response relates to the severity of the respiratory infection and time to virus clearance from the airway. Consequently, we now hypothesize that a major risk factor for asthma exacerbations with RV respiratory infections is a diminished IFN-gamma response to this virus. It is further hypothesized that diminished IFN-gamma production to RV determines the likelihood for RV to extend to the lower airway, provoke inflammation and thus exacerbate asthma. To test this hypothesis, three specific aims are established.
Specific Aim 1 will test the hypothesis that dysregulation of the immune response relates to the development of lower airway infection and inflammation. To accomplish this hypothesis, two groups of asthmatic subjects will be selected for study, one with a high peripheral blood mononuclear cell (PBMC) generation of IFN-gamma to RV and, the other, a low response. These subjects will undergo experimental RV16 inoculation and the host's response to infection will be evaluated in relationship to cold symptoms, changes in pulmonary physiology, bronchial inflammation and infection as detected in sputum or airway mucosal biopsy and generation of the cytokines/chemokines.
Specific Aim 2 will determine the mechanisms of IFN-gamma production in response to RV by identifying the cell source, nature of IFN-gamma-inducing factors, and the cell source for IFN-gamma inducing factors.
Specific Aim 3 will test the hypothesis that asthma exacerbations to a natural RV infection are related to a cytokine dysregulated response to RV. Subjects with and without an exacerbation of asthma from a natural cold will be evaluated as described in Specific Aim 1. The results from these studies may provide a new insight into the importance and mechanisms of the asthmatic subject's immune IFN-gamma production and its relationship to asthma exacerbations.

Agency
National Institute of Health (NIH)
Institute
National Institute of Allergy and Infectious Diseases (NIAID)
Type
Research Program Projects (P01)
Project #
5P01AI050500-02
Application #
6651259
Study Section
Special Emphasis Panel (ZAI1)
Project Start
2002-09-01
Project End
2003-06-30
Budget Start
Budget End
Support Year
2
Fiscal Year
2002
Total Cost
Indirect Cost
Name
University of Wisconsin Madison
Department
Type
DUNS #
161202122
City
Madison
State
WI
Country
United States
Zip Code
53715
Ludka-Gaulke, Tiffany; Ghera, Princy; Waring, Stephen C et al. (2018) Farm exposure in early childhood is associated with a lower risk of severe respiratory illnesses. J Allergy Clin Immunol 141:454-456.e4
Gavala, Monica L; Bertics, Paul J; Gern, James E (2011) Rhinoviruses, allergic inflammation, and asthma. Immunol Rev 242:69-90
Hill, Lindsay M; Gavala, Monica L; Lenertz, Lisa Y et al. (2010) Extracellular ATP may contribute to tissue repair by rapidly stimulating purinergic receptor X7-dependent vascular endothelial growth factor release from primary human monocytes. J Immunol 185:3028-34
Gern, James E (2010) The ABCs of rhinoviruses, wheezing, and asthma. J Virol 84:7418-26
Korpi-Steiner, N L; Valkenaar, S M; Bates, M E et al. (2010) Human monocytic cells direct the robust release of CXCL10 by bronchial epithelial cells during rhinovirus infection. Clin Exp Allergy 40:1203-13
Lemanske Jr, Robert F; Busse, William W (2010) Asthma: clinical expression and molecular mechanisms. J Allergy Clin Immunol 125:S95-102
Denlinger, Loren C; Shi, Lei; Guadarrama, Arturo et al. (2009) Attenuated P2X7 pore function as a risk factor for virus-induced loss of asthma control. Am J Respir Crit Care Med 179:265-70
DeMore, Jennifer P; Weisshaar, Elizabeth H; Vrtis, Rose F et al. (2009) Similar colds in subjects with allergic asthma and nonatopic subjects after inoculation with rhinovirus-16. J Allergy Clin Immunol 124:245-52, 252.e1-3
Rosenthal, Louis A; Amineva, Svetlana P; Szakaly, Renee J et al. (2009) A rat model of picornavirus-induced airway infection and inflammation. Virol J 6:122
Sorkness, Ronald L; Gonzalez-Fernandez, Guillermo; Billmeyer, Erin E et al. (2008) The asthma index: a continuous variable to characterize exacerbations of asthma. J Allergy Clin Immunol 122:838-40

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