A mechanistic role for type III IFN-?1 in asthma exacerbations mediated by human rhinoviruses.

ABSTRACT:

Rationale

Human rhinoviruses (HRV) are the leading cause of upper respiratory infections and have been postulated to trigger asthma exacerbations. However, whether HRV are detected during crises because upper respiratory infections often accompany asthma attacks, or because they specifically elicit exacerbations, is unclear. Moreover, although several hypotheses have been advanced to explain virus-induced exacerbations, their mechanism remains unclear.

Objectives

To determine the role of HRV in pediatric asthma exacerbations and the mechanisms mediating wheezing.

Methods

We prospectively studied 409 children with asthma presenting with upper respiratory infection in the presence or absence of wheezing. Candidate viral and immune mediators of illness were compared among children with asthma with different degrees of severity of acute asthma.

Measurements and main results

HRV infections specifically associated with asthma exacerbations, even after adjusting for relevant demographic and clinical variables defined a priori (odds ratio, 1.90; 95% confidence interval, 1.21-2.99; P = 0.005). No difference in virus titers, HRV species, and inflammatory or allergic molecules was observed between wheezing and nonwheezing children infected with HRV. Type III IFN-?(1) levels were higher in wheezing children infected with HRV compared with nonwheezing (P < 0.001) and increased with worsening symptoms (P < 0.001). Moreover, after adjusting for IFN-?(1), children with asthma infected with HRV were no longer more likely to wheeze than those who were HRV-negative (odds ratio, 1.18; 95% confidence interval, 0.57-2.46; P = 0.66).

Conclusions

Our findings suggest that HRV infections in children with asthma are specifically associated with acute wheezing, and that type III IFN-?(1) responses mediate exacerbations caused by HRV. Modulation of IFN- ?(1) should be studied as a therapeutic target for exacerbations caused by HRV.

SUBMITTER: Miller EK 

PROVIDER: S-EPMC3361761 | biostudies-literature | 2012 Mar

REPOSITORIES: biostudies-literature