Me. Helminen et al., HUMAN IMMUNE-RESPONSE AGAINST OUTER-MEMBRANE PROTEINS OF MORAXELLA (BRANHAMELLA) CATARRHALIS DETERMINED BY IMMUNOBLOTTING AND ENZYME-IMMUNOASSAY, Clinical and diagnostic laboratory immunology, 2(1), 1995, pp. 35-39
The role of Moraxella (Branhamella) catarrhalis as a respiratory tract
pathogen is increasingly recognized. We looked at the human immune re
sponse against individual outer membrane proteins of M. catarrhalis an
d against the 81-kDa CopB protein, which has previously been shown to
be a target far protective antibodies. Paired serum samples from six e
lderly patients with pneumonia were tested by Western blot (immunoblot
) analysis by using outer membrane vesicles of M. catarrhalis 035E as
antigen. All of the six convalescent-phase serum samples reacted with
a protein which migrated at the position of the CopB protein and with
a high-molecular-weight protein of M. catarrhalis; three serum samples
also reacted with a 34-kDa outer membrane protein. Paired serum sampl
es from 18 patients, 10 of which had M. catarrhalis infection on the b
asis of previous serology results, were tested by enzyme immunoassay (
EIA) with the CopB protein and whole cells of M. catarrhalis 035E as a
ntigens. Nine patients showed a significant rise in EIA titer between
acute- and convalescent-phase sera when whole bacterial cells were use
d as antigens. Six (67%) patient samples that were positive by the EIA
with the whole-cell antigen were also positive by the EIA with the Co
pB antigen, and six of nine patient samples negative by the EIA with t
he whole-cell antigen were also negative by the EIA with the CopB anti
gen. These results suggest that both the CopB and a high-molecular-wei
ght protein are major targets of the immune response against M. catarr
halis, and further studies with greater amounts of patient materials a
re needed to elucidate the usefulness of CopB as an antigen in etiolog
ic studies.