Episodic wheezing associated with viral infections of the upper respiratory
tract (URT) is a common problem in young children but also occurs in adult
s. It is hypothesized that an experimental infection with human coronavirus
(HCoV), the second most prevalent common cold virus, would cause lower res
piratory tract (LRT) changes in adults with a history of viral wheeze.
Twenty-four viral wheezers (15 atopic) and 19 controls (seven atopic) were
inoculated with HCoV 229E and monitored for the development of symptoms, ch
anges in airway physiology and provocative concentration of methacholine ca
using a 20% fall in forced expiratory volume in one second (FEV1) (PC20). A
t baseline, viral wheezers were similar to controls in PC20 (mean +/- SD lo
g(2)PC20: 5.1 +/-1.9 and 5.8 +/-1.4 g.L-1, respectively) but had a lower FE
V1 than controls (mean +/- SD 85.8 +/- 11.4 and 95.6 +/- 13.2% predicted, r
espectively p < 0.05). Nineteen viral wheezers and I I controls developed c
olds. Viral wheezers with colds reported significantly more URT symptoms th
an controls (median scores (interquartile range): 24 (10-37) and 6 (4-15),
respectively p = 0.014). Sixteen viral wheezers, and no controls reported L
RT symptoms (wheeze, chest tightness and shortness of breath). The viral wh
eezers; with colds had small (3-4%) reductions in FEV1 and peak expiratory
flow on days with LRT symptoms (days 3 - 6), but a progressive reduction in
PC20 from baseline on days 2, 4 and 17 after inoculation (by 0.82, 1.35 an
d 1.82 doubling concentrations, respectively). The fall in PC20 affected bo
th atopic and nonatopic subjects equally. There were no changes in FEV1 or
PC20 in controls.
An adult model of viral wheeze that is independent of atopy and therefore,
of classical atopic asthma was established.