A murine monoclonal anti-chromosomal beta-lactamase antibody was devel
oped and an immunoblotting technique was used to study the presence of
serum and sputum antibodies against Pseudomonas aeruginosa chromosoma
l group 1 beta-lactamase in patients with cystic fibrosis (CF). The se
rum antibody response was studied with serum samples collected in 1992
from 56 CF patients in a cross-sectional study and with serum samples
from 18 CF patients in a longitudinal study. Anti-beta-lactamase immu
noglobulin G antibodies were present in all of the serum samples from
the patients with chronic bronchopulnonary P. aeruginosa infection (CF
+P) but in none of the CF patients with no or intermittent P. aerugino
sa infection. Anti-beta-lactamase antibodies were present in serum fro
m CF+P patients after six antipseudomonal courses (median) and correla
ted with infection with a beta-lactam-resistant strain of P. aeruginos
a. The sputum antibody response and the beta-lactamase activity in spu
tum samples from 14 of the CF+P patients were also studied. beta-Lacta
mase antibodies were present in 10 of these samples. P. aeruginosa str
ains isolated from these samples were partially derepressed, producing
group 1 cephalosporinase. We found a wide range of chromosomal beta-l
actamase activity in the sputum samples, with no correlation with basa
l or induced activity of beta-lactamase expression. The presence of an
ti-beta-lactamase antibodies in endobronchial sputum could be an impor
tant factor in the defense against the infection. On the other hand, i
mmune complexes between beta-lactamase and corresponding antibodies co
uld play a role in the pathogenesis of bronchopulmonary injury in CF b
y mediating hyperimmune reactions.