HIGH-LEVELS OF COMPLEMENT-ACTIVATION CAPACITY IN SERA FROM PATIENTS WITH CYSTIC-FIBROSIS CORRELATE WITH HIGH-LEVELS OF IGG3 ANTIBODIES TO PSEUDOMONAS-AERUGINOSA ANTIGENS AND POOR LUNG-FUNCTION
T. Pressler et al., HIGH-LEVELS OF COMPLEMENT-ACTIVATION CAPACITY IN SERA FROM PATIENTS WITH CYSTIC-FIBROSIS CORRELATE WITH HIGH-LEVELS OF IGG3 ANTIBODIES TO PSEUDOMONAS-AERUGINOSA ANTIGENS AND POOR LUNG-FUNCTION, Pediatric pulmonology, 20(2), 1995, pp. 71-77
Heat-stable opsonins from sera of cystic fibrosis (CF) patients were i
nvestigated for their ability to activate complement. Complement activ
ation by Pseudomonas aeruginosa after opsonization with patient serum
was examined in a complement-consumption assay. Absorption of patients
' sera with formalin-treated and boiled bacteria removed specific anti
bodies and the complement activation decreased. We found a positive co
rrelation between serum complement-activation ability and IgG3 antibod
y levels to lipopolysaccharide (LPS), alginate, and a crude mixture of
P. aeruginosa antigens (sonicate) in a group of patients with high le
vels of anti-Pseudomonas precipitins. In the same group of patients a
significant negative correlation was found between complement activati
on and lung function. Eighteen patients have been followed longitudina
lly with serum samples covering the pre-infection, the early, and the
late stages of chronic infection. Patients with poor lung function sho
wed significantly higher levels of complement-activation capacity. We
conclude that patients with high levels of specific IgG3 antibodies ar
e able to induce a high level of complement activation and then develo
p more aggressive pulmonary tissue damage, probably secondary to local
immune complex formation. (C) 1995 Wiley-Liss, Inc.