UTILIZATION OF PROTEINASE K-TREATED CELLS AS LIPOPOLYSACCHARIDE ANTIGENS FOR THE SERODIAGNOSIS OF HELICOBACTER-PYLORI INFECTIONS

Citation
K. Amano et al., UTILIZATION OF PROTEINASE K-TREATED CELLS AS LIPOPOLYSACCHARIDE ANTIGENS FOR THE SERODIAGNOSIS OF HELICOBACTER-PYLORI INFECTIONS, Microbiology and immunology, 42(7), 1998, pp. 509-514
Citations number
24
Categorie Soggetti
Microbiology,Immunology
Journal title
ISSN journal
03855600
Volume
42
Issue
7
Year of publication
1998
Pages
509 - 514
Database
ISI
SICI code
0385-5600(1998)42:7<509:UOPKCA>2.0.ZU;2-K
Abstract
We have evaluated the use of proteinase K (PK)-treated cells isolated from Helicobacter pylori as lipopolysaccharide (LPS) antigens in an im munoblot assay and an enzyme-linked immunosorbent assay (ELISA) for th e serodiagnosis of H, pylori infection. The sera from patients with ch ronic gastritis, gastric ulcer, duodenal ulcer or gastric cancer, and from healthy adults with or without H. pylori infection were assayed w ith three commercial serodiagnostic kits (HM-CAP, Helico-G, and G,A,P, II) and novel methods relying on the use of PK-treated cells. The PK- treated cells used in these assays were selected on the basis of their possibility to possess a common epitope in the O-polysaccharides of H , pylori, which is known to be highly immunogenic in humans. Of the se ra from these patients, 71-94% were positive with the commercial kits, 97% with immunoblot assay, and 90% with ELISA, On the other hand, of the healthy adults infected with H, pylori, 72-97% were positive with the commercial kits, 86% with immunoblot assay, and 72% with ELISA, PK -treated cells that did not contain the common epitope were unsuitable as an antigen for immunoblot assay or ELISA, Furthermore, the reactiv ity of these sera reacted specifically with H. pylori PK-treated cells but not with LPSs from other gram-negative bacteria, such as Campylob acter, Proteus, Bordetella, and Salmonella, These results demonstrate that the serological assays relying on the use of H, pylori PK-treated cells possessing a highly antigenic epitope are potentially useful as a serodiagnostic test for H. pylori infection.