The development of nanotechnology has increased the risk of environmental exposure to types of particles other than those derived from combustion, namely, industrial nanomaterials. Patients with
bronchial asthma are sensitive to inhaled substances, including
particulate matter. This study examined the effects of pulmonary exposure to a type of nano-sized
carbon nanotube (single-walled nanotubes (SWCNT)) on allergic airway
inflammation and sought their cellular mechanisms. In the in vivo experiments, ICR mice were divided into four experimental groups that were repeatedly administered vehicle, SWCNT (50 microg/animal),
ovalbumin (OVA; an
allergen), or OVA + SWCNT through an intratracheal route and thereafter assayed. SWCNT aggravated
allergen-induced
pulmonary inflammation with mucus
hyperplasia. SWCNT with
allergen amplified lung
protein levels of T helper (Th)
cytokines and
chemokines related to
allergy and exhibited adjuvant activity for
allergen-specific
IgG(1) (and
IgE) compared with
allergen alone. SWCNT accentuated the level/activity of oxidative stress-related
biomarkers in the airways in the presence of
allergen. In vitro, SWCNT can partially promote/strengthen the maturation/activation/function of bone marrow-derived dendritic cells (DC). Together, these results suggest that SWCNT can exacerbate murine allergic airway
inflammation via enhanced activation of Th immunity and increased oxidative stress. In addition, this exacerbation may be partly through the inappropriate activation of antigen-presenting cells, including DC.