B. Wallaert et al., IMMUNOREACTIVITY FOR INTERLEUKIN-3 AND INTERLEUKIN-5 AND GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR OF INTESTINAL-MUCOSA IN BRONCHIAL-ASTHMA, The Journal of experimental medicine, 182(6), 1995, pp. 1897-1904
T lymphocytes and eosinophils are important components of the inflamma
tory cell infiltrate in bronchial mucosa in asthma. Because activated
lymphocytes migrate through the thoracic duct and the general circulat
ion to remote glandular and mucosal sites, we initiated this study to
evaluate pathological abnormalities and immunoreactivity for interleuk
in (IL) 3, IL-5, and granulocyte/macrophage colony-stimulating factor
(GM-CSF) of intestinal mucosa in bronchial asthma. 15 asthmatic patien
ts, 8 nonasthmatic patients with chronic obstructive pulmonary disease
, 6 atopic nonasthmatic healthy controls, and 6 nonatopic healthy cont
rols were studied. Duodenal biopsies were performed by endoscopy. A si
gnificantly increased number of intraepithelial lymphocytes and eosino
phils and a significant accumulation of mononuclear cells (lymphocytes
and mast cells) and eosinophils in the lamina propria were detected i
n asthmatics and atopic controls. Immunostaining with antibodies direc
ted against IL-3, IL-5, and GM-CSF was positive in asthmatics and atop
ic controls, whereas no staining was observed in nonatopic controls an
d chronic obstructive pulmonary disease. Combined ultrastructural stud
y and immunogold labeling demonstrated that IL-3, IL-5, and GM-CSF wer
e localized in eosinophils and mast cells. Although devoid of gastroin
testinal symptoms, asthmatics and asymptomatic atopics had duodenal pa
thological abnormalities mimicking those observed in the bronchial muc
osa in asthma, suggesting that the whole mucosal immune system is invo
lved in bronchial asthma.