The gastric H+,K+-ATPase is a major autoantigen in chronic Helicobacter pylori gastritis with body mucosa atrophy

被引:195
作者
Claeys, D
Faller, G
Appelmelk, BJ
Negrini, R
Kirchner, T
机构
[1] Univ Erlangen Nurnberg, Inst Pathol, D-91054 Erlangen, Germany
[2] Inst Biochem, Lausanne, Switzerland
[3] Swiss Inst Expt Canc Res, Lausanne, Switzerland
[4] Vrije Univ Amsterdam, Dept Med Microbiol, Amsterdam, Netherlands
[5] Spedali Civili, Lab Clin Chem 3, I-25125 Brescia, Italy
关键词
D O I
10.1016/S0016-5085(98)70200-8
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: A subgroup of Helicobacter pylori-infected patients develops autoantibodies to gastric parietal cell canaliculi. The aim of this study was to define the unknown autoantigen. Methods: We screened 72 H. pylori-infected patients, 5 patients with autoimmune gastritis, and 36 healthy controls for immunoglobulin G autoantibodies to canaliculi by immunohistochemistry. The antigen specificity was determined by immunoprecipitation of the murine gastric H+,K+-adenosine triphosphatase (H+,K+-ATPase) expressed in oocytes and by immunoblotting on human gastric membranes from the body mucosa. Results: Autoantibodies specific for the conformational peptides of the H+,K+-ATPase were detected in 3% (1/36) of controls, in all patients with autoimmune gastritis (5/5), in 25% (18/72) of H. pylori-infected patients, and in 47% (15/32) of the infected patients with anticanalicular autoantibodies. No other major autoantigen was identified. Atrophy in the gastric body mucosa was found in 60% (9/15) of infected patients with both anticanalicular and anti-H+,K+-ATPase antibodies, but only in 13% (5/37) of infected patients lacking both autoantibodies (P < 0.01). Conclusions: The gastric H+,K+-ATPase is a major autoantigen in H. pylori-associated antigastric autoimmunity. Thus, anti-H+,K+-ATPase autoantibodies, which are closely linked to classical autoimmune gastritis, are also significant indicators for body mucosa atrophy in chronic H. pylori gastritis.
引用
收藏
页码:340 / 347
页数:8
相关论文
共 34 条
[1]   Reactivities of Lewis antigen monoclonal antibodies with the lipopolysaccharides of Helicobacter pylori strains isolated from patients with gastroduodenal diseases in Japan [J].
Amano, K ;
Hayashi, S ;
Kubota, T ;
Fujii, N ;
Yokota, S .
CLINICAL AND DIAGNOSTIC LABORATORY IMMUNOLOGY, 1997, 4 (05) :540-544
[2]   Molecular mimicry between Helicobacter pylori and the host [J].
Appelmelk, BJ ;
Negrini, R ;
Moran, AP ;
Kuipers, EJ .
TRENDS IN MICROBIOLOGY, 1997, 5 (02) :70-73
[3]   Potential role of molecular mimicry between Helicobacter pylori lipopolysaccharide and host Lewis blood group antigens in autoimmunity [J].
Appelmelk, BJ ;
SimoonsSmit, I ;
Negrini, R ;
Moran, AP ;
Aspinall, GO ;
Forte, JG ;
DeVries, T ;
Quan, H ;
Verboom, T ;
Maaskant, JJ ;
Ghiara, P ;
Kuipers, EJ ;
Bloemena, E ;
Tadema, TM ;
Townsend, RR ;
Tyagarajan, K ;
Crothers, JM ;
Monteiro, MA ;
Savio, A ;
DeGraaff, J .
INFECTION AND IMMUNITY, 1996, 64 (06) :2031-2040
[4]   Lipopolysaccharide of the Helicobacter pylori type strain NCTC 11637 (ATCC 43504): Structure of the O antigen chain and core oligosaccharide regions [J].
Aspinall, GO ;
Monteiro, MA ;
Pang, H ;
Walsh, EJ ;
Moran, AP .
BIOCHEMISTRY, 1996, 35 (07) :2489-2497
[5]   Lipopolysaccharides of Helicobacter pylori strains P466 and MO19: Structures of the O antigen and core oligosaccharide regions [J].
Aspinall, GO ;
Monteiro, MA .
BIOCHEMISTRY, 1996, 35 (07) :2498-2504
[6]   HELICOBACTER-PYLORI INFECTION IN PEPTIC-ULCER DISEASE [J].
BERSTAD, K ;
BERSTAD, A .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1993, 28 (07) :561-567
[7]   PARIETAL-CELL ANTIBODIES IN PERNICIOUS-ANEMIA INHIBIT H+,K+-ADENOSINE TRIPHOSPHATASE, THE PROTON PUMP OF THE STOMACH [J].
BURMAN, P ;
MARDH, S ;
NORBERG, L ;
KARLSSON, FA .
GASTROENTEROLOGY, 1989, 96 (06) :1434-1438
[8]  
CALLAGHAN JM, 1992, BIOCHEM J, V283, pG3
[9]   Neonatal injection of native proton pump antigens induces autoimmune gastritis in mice [J].
Claeys, D ;
Saraga, E ;
Rossier, BC ;
Kraehenbuhl, JP .
GASTROENTEROLOGY, 1997, 113 (04) :1136-1145
[10]  
Correa P, 1980, Front Gastrointest Res, V6, P98