Awardee OrganizationUNIVERSITY OF WISCONSIN-MADISON
Description
Abstract Text
Infections with viruses, and rhinoviruses in particular, are major causes of asthma exacerbations, and
account for a large percentage of the morbidity and economic costs associated with asthma. Current
asthma treatment, although effective in the control of allergic asthma, is not always capable of preventing
exacerbations of wheezing due to respiratory infections. Based on this unmet clinical need, we propose a
program of multifaceted and highly interactive studies to establish the mechanisms by which RV cause
exacerbations of asthma. The severity of viral infections and their effects on the lower airway are dependent
on factors related to the virus and the host. Our overall hypothesis is that the severity of RV infections
and resulting airway dysfunction is critically dependent on a) the interplay between RV replication in
the epithelial cell and early innate antiviral responses, and b) variations in the host regulation of proinflammatory
and antiviral responses to infection. Our previous work has focused primarily on the ability
of RV to infect the lower airway, upregulate inflammation and thereby initate lower airway obstruction and
symptoms. The differential nature of these responses may well determine why certain individuals have
significant exacerbations of asthma with virus infections, while others simply have clinical "colds." We now
propose five interactive and innovative projects that involve mechanistic studies in isolated populations of
cells, and in vivo models in both the human and the mouse. The in vitro projects include experiments to
define virus-induced mechanisms of macrophage priming (Project by Bertics), recruitment and activation of
neutrophils into the airway (Project by Huttenlocher), and the destruction of epithelial cell nuclear pores to divert cellular
metabolism towards viral protein synthesis and replication (Project by Palmenberg). These in vitro studies are
complemented by two in vivo models: a genetics study to identify associations with clinical and biologic
outcomes of experimentally-induced RV infection (Project by Gern), and a murine model of picornavirus
(mengovirus) infection to evaluate mechanisms of virus-induced cellular inflammation. These projects'
approach to identify critical host/virus interactions that determine the severity of illness and respiratory
dysfunction are synergistic, interactive, and take advantage of a unique set of resources and decades of
published experience in this area found at the University of Wisconsin. Collectively, these will studies
address clinically relevant gaps in our current understanding of virus-induced airway dysfunction and
facilitate the development of new and more efficacious therapeutic strategies.
Lav Summary: Infections with rhinovirus, a common cold virus, are the major cause of asthma
exacerbations in children, and continue to be a problem for adults with asthma. The goal of this project is to
determine why this is so, and identify new approaches to either prevent or treat rhinovirus-induced asthma.
National Institute of Allergy and Infectious Diseases
CFDA Code
DUNS Number
161202122
UEI
LCLSJAGTNZQ7
Project Start Date
01-July-2006
Project End Date
31-August-2011
Budget Start Date
01-July-2006
Budget End Date
31-August-2007
Project Funding Information for 2006
Total Funding
$212,334
Direct Costs
$161,565
Indirect Costs
$50,769
Year
Funding IC
FY Total Cost by IC
2006
National Institute of Allergy and Infectious Diseases
$212,334
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 1U19AI070503-01 0001
Publications
Publications are associated with projects, but cannot be identified with any particular year of the project or fiscal year of funding. This is due to the continuous and cumulative nature of knowledge generation across the life of a project and the sometimes long and variable publishing timeline. Similarly, for multi-component projects, publications are associated with the parent core project and not with individual sub-projects.
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Outcomes
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