To examine the role of the bronchial microvasculature and adhesion molecule
expression in severe asthma, the authors have performed an immunohistochem
ical study on bronchial biopsies comparing 15 glucocorticoid-dependent asth
matics, 15 mild asthmatics and eight control subjects.
Serially cut glycol methacrylate-embedded sections were stained with monocl
onal antibodies identifying the vessel marker EN-4, intercellular adhesion
molecule (ICAM)-1, vascular cell adhesion molecule (VCAM)-1. E- and P-selec
tin, Sections were also stained for lymphocyte function associated antigen
(LFA)-1 and very late antigen (VLA)-4.
By comparison with mild asthma and nonasthma, severe asthma was characteriz
ed by increased numbers of submucosal vessels (p=0.009) which was associate
d with increased numbers of vessels expressing ICAM-1 (p=0.005). A highly s
ignificant correlation was found between the total number of EN-4+ vessels
and the vessels expressing ICAM-1 (r=0.85, p=0.01), in contrast, E-selectin
expression was lower in severe as compared with mild asthma (p=0.01) but n
ot different from normal. No differences were found between the three group
s in the expression of VCAM-1 and P-selectin nor in numbers of LFA-1+ and V
LA-4+ cells.
The results of this study support the notion that mucosal neovascularizatio
n is an important feature of airways remodelling in severe asthma. This is
associated with a relatively higher density of vessels expressing intercell
ular adhesion molecule-1, although the expression of this adhesion molecule
per vessel was not raised.