C. Pilette et al., Reduced epithelial expression of secretory component in small airways correlates with airflow obstruction in chronic obstructive pulmonary disease, AM J R CRIT, 163(1), 2001, pp. 185-194
The epithelial polymeric immunoglobulin receptor/transmembrane secretory co
mponent (plgR/SC) transports into secretions polymeric immunoglobulin A (pl
gA), which is considered the first line of defense of the respiratory tract
. The present study, done with quantitative immunohistochemistry, evaluated
epithelial expression of secretory component (SC) and Clara cell protein (
CC16) and neutrophil infiltration into the airways of eight patients with s
evere chronic obstructive pulmonary disease (COPD) who were undergoing lung
transplantation, as compared with these processes in six nonsmoking patien
ts with pulmonary hypertension who were used as controls and in lung specim
ens from five smokers without chronic bronchitis. Staining for SC was signi
ficantly decreased in the COPD patients as compared with the controls, both
in large (mean optical density [MOD]: 23.4 [range: 21.1 to 27.8] Versus 42
.2 [range: 28.2 to 49.3], p = 0.003) and in small airways (MOD: 30.8 [range
: 20.3 to 39.4] versus 41.5 [range: 39.2 to 46.2], p = 0.003). SC expressio
n in small airways correlated strongly with functional parameters such as F
EV, (Kendall's tau (K) = 0.76, p = 0.008), FVC (K = 0.64, p = 0.03), and mi
dexpiratory flow at 50% of VC (MEF50) (K = 0.74, p = 0.01). The reduced exp
ression of SC in large airways correlated with neutrophil infiltration in s
ubmucosal glands (K = -0.47, p = 0.03). Expression of CC16 in the bronchial
epithelium of COPD patients was also significantly decreased as compared w
ith that of controls, especially in small airways (MOD: 28.3 [range: 26.8 t
o 32.4] versus 45.8 [range: 40.7 to 56.0], p = 0.002), but no correlation w
as observed with lung function tests. In conclusion, this study shows that
reduced expression of SC in airway epithelium is associated with airflow ob
struction and neutrophil infiltration in severe COPD.