C. Svensson et al., ALLERGEN CHALLENGE-INDUCED ENTRY OF ALPHA(2)-MACROGLOBULIN AND TRYPTASE INTO HUMAN NASAL AND BRONCHIAL AIRWAYS, Journal of allergy and clinical immunology, 96(2), 1995, pp. 239-246
Background: Microvascular-epithelial exudation of bulk plasma may char
acterize inflammatory airway diseases. This study compares the acute a
llergen challenge-induced mast cell and exudative responses in nasal n
ad bronchial airways. The focus is on alpha(2)-macroglobulin as an ind
ex of luminal entry of plasma exudates. Methods: Separate nasal and br
onchial allergen challenges were carried out outside the pollen season
in eight patients with pollen-induced seasonal allergic rhinitis. The
levels of different-sized plasma proteins (albumin molecular weight,
66,000 d and alpha(2)-macroglobulin molecular weight, 725,000 d) and t
ryptase were determined in pre- and postchallenge nasal lavage and bro
nchoalveolar lavage (BAL) fluids. Diluent and increasing doses of alle
rgen were sprayed into the right nasal cavity, and each challenge was
followed by a nasal lavage (volume, 15 ml) with a ''nasal pool'' devic
e (recovery, >80%). Endobronchial allergen challenge (individual doses
) and BAL (volume, 2 x 25 ml) were performed in a lobe bronchus throug
h a fiberoptic bronchoscope (recovery, 30%). Saline challenge and BAL
were carried out in the contralateral lung as control. Results: The le
vels of albumin, alpha(2)-macroglobulin, and tryptase increased dose-d
ependently in postchallenge and nasal lavage fluids (p < 0.05) and cor
related to nasal symptoms. In particular, albumin and alpha(2)-macrogl
obulin correlated (r = 0.98, p < 0.001). Both alpha(2)-macroglobulin a
nd tryptase, but not albumin, were increased in BAL fluids from the al
lergen-challenged side (p < 0.05). Conclusion: Local allergen challeng
e causes luminal entry of tryptase and alpha(2)-macroglobulin in the n
ose and bronchi of patients with allergy. We suggest that mass cell an
d plasma exudation responses may be similar in human nasal and bronchi
al airways and that albumin levels (in BAL fluids) may not well reflec
t the exudation process in bronchial airways