Lack of correlation between Lewis antigen expression by Helicobacter pylori and gastric epithelial cells in infected patients

被引:70
作者
Taylor, DE
Rasko, DA
Sherburne, R
Ho, C
Jewell, LD
机构
[1] Univ Alberta, Dept Med Microbiol & Immunol, Edmonton, AB T6G 2H7, Canada
[2] Univ Alberta, Walter C Mackenzie Hlth Sci Ctr, Dept Lab Med & Pathol, Edmonton, AB T6G 2H7, Canada
关键词
D O I
10.1016/S0016-5085(98)70082-4
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims: Lewis antigens are expressed by both human gastric epithelial tissue and Helicobacter pylori. We examined Lewis antigens expressed by gastric epithelium and by H. pylori isolated from the corresponding biopsy tissue. Methods: H. pylori Lewis expression was determined by enzyme immunoassays, and immunoelectron microscopy was used to confirm the Lewis antigens on some H. pylori cells and in some biopsy specimens. Histopathology using identical monoclonal antibodies specific for Lewis A, B, X, and Y antigens was used to detect these antigens in 24 gastric biopsy specimens. Results: We identified Lewis Y in 100%, Lewis X and Lewis B in 95.8%, and Lewis A in 87.5% of biopsy specimens. In H. pylori, 87.5% expressed Lewis Y, 79.2% Lewis X, and 4.2% tone strain) Lewis B. No Lewis A was detected. Antibody specific for Lewis X labeled the bacteria and associated adhesion pedestal. The cagA gene was present in 92% of strains. Conclusions: There was no direct relationship between Lewis antigen expression by H. pylori and gastric epithelial cells in infected patients. Expression of Lewis X and Lewis Y by H. pylori suggests the possibility of their requirement for establishment and/or maintenance of infection. An immunoelectron micrograph of H. pylori interaction with the gastric epithelial adhesion pedestal suggests a tentative role for Lewis X in the adhesion process.
引用
收藏
页码:1113 / 1122
页数:10
相关论文
共 31 条
[1]   OBSERVER VARIATION IN THE ASSESSMENT OF CHRONIC GASTRITIS ACCORDING TO THE SYDNEY SYSTEM [J].
ANDREW, A ;
WYATT, JI ;
DIXON, MF .
HISTOPATHOLOGY, 1994, 25 (04) :317-322
[2]  
ASPINALL GO, 1994, CARBOHYDR LETT, V0001
[3]   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
[4]   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
[5]   ATTACHMENT OF HELICOBACTER-PYLORI TO HUMAN GASTRIC EPITHELIUM MEDIATED BY BLOOD-GROUP ANTIGENS [J].
BOREN, T ;
FALK, P ;
ROTH, KA ;
LARSON, G ;
NORMARK, S .
SCIENCE, 1993, 262 (5141) :1892-1895
[6]   Aberrant expression of gland-type gastric mucin in the surface epithelium of Helicobacter pylori - Infected patients [J].
Byrd, JC ;
Yan, PS ;
Sternberg, L ;
Yunker, CK ;
Scheiman, JM ;
Bresalier, RS .
GASTROENTEROLOGY, 1997, 113 (02) :455-464
[7]   cag, a pathogenicity island of Helicobacter pylori, encodes type I-specific and disease-associated virulence factors [J].
Censini, S ;
Lange, C ;
Xiang, ZY ;
Crabtree, JE ;
Ghiara, P ;
Borodovsky, M ;
Rappuoli, R ;
Covacci, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (25) :14648-14653
[8]   THE BIOSYNTHESIS OF LEWIS-X IN HELICOBACTER-PYLORI [J].
CHAN, NWC ;
STANGIER, K ;
SHERBURNE, R ;
TAYLOR, DE ;
ZHANG, YN ;
DOVICHI, NJ ;
PALCIC, MM .
GLYCOBIOLOGY, 1995, 5 (07) :683-688
[9]   IMMUNOHISTOLOGIC EXPRESSION OF BLOOD-GROUP ANTIGENS IN NORMAL HUMAN GASTROINTESTINAL-TRACT AND COLONIC-CARCINOMA [J].
CORDONCARDO, C ;
LLOYD, KO ;
SAKAMOTO, J ;
MCGROARTY, ME ;
OLD, LJ ;
MELAMED, MR .
INTERNATIONAL JOURNAL OF CANCER, 1986, 37 (05) :667-676
[10]  
Cover TL, 1996, ADV INTERNAL MED, V41, P85