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Clinical and Diagnostic Laboratory Immunology, 09 1997, 540-544, Vol 4, No. 5
K Amano, S Hayashi, T Kubota, N Fujii and S Yokota
We have examined the reactivity of monoclonal antibodies (MAbs) specific
for Lewis antigens (Le(x), Le(y), Le(a), and Le(b)) with Helicobacter
pylori lipopolysaccharides (LPS) by immunoblot analysis and enzyme-linked
immunosorbent assay (ELISA). Sixty-eight strains of H. pylori were isolated
from patients with chronic gastritis, gastric and duodenal ulcers, and
gastric cancer in Japan. The cells were treated with proteinase K, and the
resulting fractions were used as a source of LPS for the immunoassays. In
the immunoblot analysis, 28 isolates (41%) and 29 isolates (42%) reacted
with anti-Le(x) and anti- Le(y) MAbs, respectively, while 4 isolates (6%)
and 7 isolates (10%) reacted with anti-Le(a) and anti-Le(b) MAbs. On the
other hand, in ELISA, the number of isolates that reacted with anti-Le(x)
MAbs fell significantly to 21 isolates (30%) but the number of isolates
that reacted with the other anti-Lewis antigen MAbs remained relatively
unchanged. These data show that the immunoblotting technique is more
sensitive than the ELISA technique for the detection of immunocomplexes of
anti-Le(x) MAbs and components of H. pylori LPS. Furthermore, human serum
was found to react with the synthetic Lewis antigens regardless of the
status of the individual's H. pylori infection. This means that humans may
naturally possess antibodies against Lewis antigens in the absence of H.
pylori infection.
Copyright © 1997 by the American Society for Microbiology. All rights reserved.
Reactivities of Lewis antigen monoclonal antibodies with the lipopolysaccharides of Helicobacter pylori strains isolated from patients with gastroduodenal diseases in Japan
Central Research Laboratory, Akita University School of Medicine, Japan. amanocrl@med.akita-u.ac.jp
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