Serological differentiation of H. pylori CagA(+) and CagA(-) infections

• Authors: M. Chmiela , M. Wisniewska , L. Bak-Romaniszyn , T. Rechcinski , I. Planeta-Malecka , W. Bielanski , S.J. Konturek , M. Plonka , M. Klink , W. Rudnicka
• Languages of publication: EN

Abstracts

EN

Many of H. pylori strains causing gastroduodenal diseases have a cagA gene encoding CagA protein, a virulence factor of these bacteria. Anti-CagA antibodies produced by majority of people infected with CagA(+) strains can indicate such infection. In this study the efficacy of three immunoenzymatic tests: immunoblot (MileniaID Blot H. pylori IgG, DPC Biermann GmbH, Germany) (MB) and ELISA, conducted with a recombinant immunodominant fragment of CagA (rCagA) and full length CagA molecule (flCagA), in detecting CagA(+) and CagA(-) infections, was compared. The 13C urea breath test (13C-UBT) was used for establishing H. pylori status. The serum samples from 157 individuals were used for serodiagnosis. The H. pylori CagA(+) infection was detected in H. pylori infected individuals with similar frequency by MB (64%) and flCagA-ELISA (60%) and little less frequently by rCagA-ELISA (53%). There was a high coincidence between the negative results of these three tests for H. pylori uninfected individuals with no anti-CagA IgG in the serum (96-100%). The results show that rCagA-ELISA and especially flCagA-ELISA are easy, inexpensive and useful noninvasive assays for discrimination of CagA(+) and CagA(-) H. pylori infections in the subjects examined by urea breath test.

Keywords

EN

HELICOBACTER PYLORI; SERODIAGNOSIS

Discipline

• IMMUNOLOGY: IMMUNOLOGY

• Journal: Archivum Immunologiae et Therapiae Experimentalis
• Year: 2003
• Volume: 51
• Issue: 2
• Pages: 131-136

Contributors

author

M. Chmiela

author

M. Wisniewska

author

L. Bak-Romaniszyn

author

T. Rechcinski

author

I. Planeta-Malecka

author

W. Bielanski

author

S.J. Konturek

author

M. Plonka

author

M. Klink

author

W. Rudnicka

• Document Type: SHORT COMMUNICA
• Publication order reference: M. Chmiela, Department of Immunology and Infectious Biology, University of Lodz, Banacha 12/16, 90-237 Lodz, Poland