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Divisions of Pulmonary Medicine and Allergy, Immunology, and Infectious Diseases, Joseph Stokes, Jr. Research Institute, Children's Hospital of Philadelphia, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104
To elucidate the mechanistic
interplay between rhinovirus (RV) exposure and atopic sensitization in
regulating airway smooth muscle (ASM) responsiveness, isolated rabbit
ASM tissue and cultured human ASM cells were passively sensitized with
sera from atopic asthmatic or nonatopic nonasthmatic (control) subjects
in the absence and presence of inoculation with RV serotype 16. Relative to control subjects, atopic asthmatic serum-sensitized and
RV-inoculated ASM exhibited significantly increased contractility to
acetylcholine, impaired relaxation to isoproterenol, and enhanced
release of the proinflammatory cytokine interleukin-1
. These effects
were potentiated in atopic asthmatic serum-sensitized ASM concomitantly inoculated with RV and inhibited by pretreating the tissues with monoclonal blocking antibodies against intercellular adhesion molecule
(ICAM)-1 (CD54), the host receptor for RV serotype 16, or lymphocyte
function-associated antigen (LFA)-1 (CD11a/CD18), the endogenous
counterreceptor for ICAM-1. Moreover, RV inoculation was found to
potentiate the induction of mRNA and surface protein expression of
Fc
RII (CD23), the low-affinity receptor for IgE, in atopic asthmatic
serum-sensitized ASM. Collectively, these observations provide new
evidence demonstrating that 1) RV exposure and atopic
sensitization act cooperatively to potentiate induction of proasthmatic
changes in ASM responsiveness in association with upregulated
proinflammatory cytokine release and Fc
RII expression and
2) the effects of RV exposure and atopic sensitization are mediated by cooperative ICAM-1-coupled LFA-1 signaling in the ASM itself.
asthma; viral infection; cell adhesion molecules; cytokines; Fc receptors
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