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Journal of Clinical Microbiology, April 1998, p. 931-936, Vol. 36, No. 4
0095-1137/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
Use of Immunoblot Assay To Define Serum Antibody
Patterns Associated with Helicobacter pylori Infection and
with H. pylori-Related Ulcers
P.
Aucher,1
M. L.
Petit,2
P. R.
Mannant,3
L.
Pezennec,1
P.
Babin,2 and
J. L.
Fauchere1,*
Department of Microbiology (EA
1720),1
Department of
Pathology,2 and
Department of
Hepato-Gastro-Enterology,3 Centre Hospitalier et
Universitaire, Poitiers, France
Received 7 April 1997/Returned for modification 31 July
1997/Accepted 8 January 1998
Serology has been used worldwide to detect Helicobacter
pylori infection. Using an immunoblot assay with an antigen from
strain ATCC 43579, we sought to determine the antibodies which were
good markers of colonization and the antibody patterns associated with ulcers or atrophy. Out of 98 dyspeptic patients, 41 were colonized by
H. pylori, based on a positive culture or on positive
results of both a urease test and direct examination. These 41 patients were seropositive by an enzyme immunoassay, and 12 of them had ulcers
and 29 had evidence of atrophy. Fifty-seven of the 98 patients were
noncolonized. Twenty-five of the 57 had evidence of gastric atrophy,
and 10 were seropositive; 5 of these 10 had ulcers. By Western blot
analysis, 12 antibodies were significantly more frequent in sera from
colonized patients, and they produced immunoreactive bands at 125, 87, 74, 66, 54, 48, 46, 42, 35, 30, 16 and 14 kDa. The presence of at least
one band at 54, 35, or 42 kDa was the best marker of infection
(sensitivity, 95%; specificity, 82%). In the group of colonized
patients, none of the antibody patterns were correlated to gastric
atrophy. Conversely, the presence of a band at 125, 87, or 35 kDa was
statistically associated with the presence of an ulcer. The
simultaneous presence of bands at 87 and 35 kDa predicted the risk of
ulcers with 83% sensitivity and 69% specificity. By using
CagA-positive and VacA-positive strains and CagA-negative and
VacA-negative isogenic mutants, the antigens corresponding to the bands
at 125 and 87 kDa were shown to be CagA and VacA, respectively. On the
other hand, the 35-kDa antigen is a novel uncharacterized component of
H. pylori. These results may help to optimize the
composition of antigenic preparations for serologic detection of
H. pylori colonization. Immunoblot assay would be useful
for screening patients at high risk of ulcers.
*
Corresponding author. Mailing address: Laboratoire de
Microbiologie A, CHU La Milétrie, BP 577, 86021 Poitiers, France.
Phone: 05 49 44 43 53. Fax: 05 49 44 38 88. E-mail:
j.l.fauchere{at}chu.univ-poitiers.fr.
Journal of Clinical Microbiology, April 1998, p. 931-936, Vol. 36, No. 4
0095-1137/98/$04.00+0
Copyright © 1998, American Society for Microbiology. All rights reserved.
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