Association between Chronic Atrophic Gastritis and Serum Antibodies to 15 Helicobacter pylori Proteins Measured by Multiplex Serology

被引:55
作者
Gao, Lei [1 ]
Weck, Melanie N. [1 ]
Michel, Angelika [2 ]
Pawlita, Michael [2 ]
Brenner, Hermann [1 ]
机构
[1] German Canc Res Ctr, Div Clin Epidemiol & Aging Res, D-69115 Heidelberg, Germany
[2] German Canc Res Ctr, Div Genome Modificat & Carcinogenesis, D-69115 Heidelberg, Germany
关键词
VIRULENCE FACTORS; INCREASED RISK; INFECTION; CANCER; CAGA; IDENTIFICATION; ANTIGENS; IMMUNOPROTEOMICS; SEROPOSITIVITY; IMMUNIZATION;
D O I
10.1158/0008-5472.CAN-08-3477
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Infection with Helicobacter pylori is a major risk factor for chronic atrophic gastritis (CAG), a precursor lesion of intestinal gastric cancer. The pathogenicity of the bacterium is thought to play an important role in determining the extent and severity of clinical outcome. We aimed to assess the associations between CAG and the serostatus of antibodies to 15 H. pylori proteins. The analyses were based on 534 cases with serologically defined CAG and 1,068 age-matched and sex-matched controls participating in a population-based study conducted in Saarland, Germany among 9,953 men and women ages 50 to 74 years. A newly developed H. pylori multiplex serology method was used to detect antibodies specific to 15 H. pylori antigens. Significant associations were observed between seropositivity for all 15 specific antibodies and the presence of CAG. Exclusion of severe cases, who might have lost the infection in the course of CAG progression, substantially increased the observed associations. In H. pylori-seropositive subjects, cytotoxin-associated gene A (CagA), vacuolating toxin (VacA), helicobacter cysteine-rich protein C (HcpC), and the chaperonin GroEL were identified as independent virulence factors for CAG with adjusted odds ratios (95% confidence interval) of 3.52 (2.01-6.10), 3.19 (1.44-7.05), 4.03 (1.53-10.65), and 2.65 (1.06-6.62), respectively; the simultaneous presence of all four independent virulence factors was associated with an 18-fold risk of CAG. In conclusion, HcpC and GroEL were identified as new independent virulence factors, and in combination with the established virulence factors, CagA and VacA, were strongly associated with CAG. [Cancer Res 2009;69(7):2973-80]
引用
收藏
页码:2973 / 2980
页数:8
相关论文
共 52 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]   Novel antigens of Helicobacter pylori correspond to ulcer-related antibody pattern of sera from infected patients [J].
Atanassov, C ;
Pezennec, L ;
d'Alayer, J ;
Grollier, G ;
Picard, B ;
Fauchère, JL .
JOURNAL OF CLINICAL MICROBIOLOGY, 2002, 40 (02) :547-552
[3]   GroEL of Lactobacillus johnsonii La1 (NCC 533) is cell surface associated:: Potential role in interactions with the host and the gastric pathogen Helicobacter pylori [J].
Bergonzelli, GE ;
Granato, D ;
Pridmore, RD ;
Marvin-Guy, LF ;
Donnicola, D ;
Corthésy-Theulaz, IE .
INFECTION AND IMMUNITY, 2006, 74 (01) :425-434
[4]   HELICOBACTER-PYLORI AND THE PATHOGENESIS OF GASTRODUODENAL INFLAMMATION [J].
BLASER, MJ .
JOURNAL OF INFECTIOUS DISEASES, 1990, 161 (04) :626-633
[5]   Epidemiologic findings on serologically defined chronic atrophic gastritis strongly depend on the choice of the cutoff-value [J].
Brenner, Hermann ;
Rothenbacher, Dietrich ;
Weck, Melanie N. .
INTERNATIONAL JOURNAL OF CANCER, 2007, 121 (12) :2782-2786
[6]  
CORREA P, 1975, LANCET, V2, P58
[7]   Carcinogenesis of Helicobacter pylori [J].
Correa, Pelayo ;
Houghton, Jeanmarie .
GASTROENTEROLOGY, 2007, 133 (02) :659-672
[8]  
Corthésy-Theulaz IE, 1998, INFECT IMMUN, V66, P581
[9]   Helicobacter pylori virulence and genetic geography [J].
Covacci, A ;
Telford, JL ;
Del Giudice, G ;
Parsonnet, J ;
Rappuoli, R .
SCIENCE, 1999, 284 (5418) :1328-1333
[10]   Characterization of the Helicobacter pylori cysteine-rich protein A as a T-helper cell type 1 polarizing agent [J].
Deml, L ;
Aigner, M ;
Decker, J ;
Eckhardt, A ;
Schütz, C ;
Mittl, PRE ;
Barabas, S ;
Denk, S ;
Knoll, G ;
Lehn, N ;
Schneider-Brachert, W .
INFECTION AND IMMUNITY, 2005, 73 (08) :4732-4742