Helicobacter pylori and Schistosoma japonicum co-infection in a Chinese population:: helminth infection alters humoral responses to H-pylori and serum pepsinogen I/II ratio

被引:34
作者
Du, YQ
Agnew, A
Ye, XP
Robinson, PA
Forman, D
Crabtree, JE
机构
[1] St James Univ Hosp, Mol Med Unit, Leeds LS9 7TF, W Yorkshire, England
[2] Univ Leeds, Dept Biol, Leeds, W Yorkshire, England
[3] Second Mil Med Univ, Changhai Hosp, Dept Gastroenterol, Shanghai, Peoples R China
基金
英国惠康基金;
关键词
Helicobacter pylori; CagA; helminth; Schistosoma japonicum; pepsinogen; gastric atrophy;
D O I
10.1016/j.micinf.2005.05.017
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The effects of helminth infection on humoral I-G responses and clinical outcome of gastric Helicobacter pylori infection are unknown. IgG and IgG subclass responses to H. pylori and serum pepsinogen I/II ratio, a marker of gastric atrophy, were investigated in a Schistosoma japonicum prevalent Chinese population. H. pylori, CagA and IgG subclass responses were assayed by ELISA. Serum pepsinogen I and pepsinogen II were assayed by ELISA and the pepsinogen I/II ratio determined. In 150 subjects, infection with S. japonicum and H. pylori was 55.3% and 51.3%, respectively. H. pylori IgG titres and CagA seropositivity were significantly lower (P < 0.05) in co-infected subjects, and differences in H. pylori IgG isotype responses were evident. In H. pylori positives, a significantly higher (P < 0.05) pepsinogen I/II ratio was observed in co-infected subjects. The difference between S. japonicum positive and negative subjects was only evident in H. pylori CagA seronegative subjects. In conclusion, S. japonicum co-infection with H. pylori is associated with alterations in IgG responses to H. pylori and less gastric atrophy. (c) 2005 Elsevier SAS. All rights reserved.
引用
收藏
页码:52 / 60
页数:9
相关论文
共 54 条
[1]   Analyses of the cag pathogenicity island of Helicobacter pylori [J].
Akopyants, NS ;
Clifton, SW ;
Kersulyte, D ;
Crabtree, JE ;
Youree, BE ;
Reece, CA ;
Bukanov, NO ;
Drazek, ES ;
Roe, BA ;
Berg, DE .
MOLECULAR MICROBIOLOGY, 1998, 28 (01) :37-53
[2]   Why Helicobacter pylori has Lewis antigens [J].
Appelmelk, BJ ;
Monteiro, MA ;
Martin, SL ;
Moran, AP ;
Vandenbrouck-Grauls, CMJE .
TRENDS IN MICROBIOLOGY, 2000, 8 (12) :565-570
[3]   MOSAICISM IN VACUOLATING CYTOTOXIN ALLELES OF HELICOBACTER-PYLORI - ASSOCIATION OF SPECIFIC VACA TYPES WITH CYTOTOXIN PRODUCTION AND PEPTIC-ULCERATION [J].
ATHERTON, JC ;
CAO, P ;
PEEK, RM ;
TUMMURU, MKR ;
BLASER, MJ ;
COVER, TL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (30) :17771-17777
[4]  
Beales ILP, 1996, EUR J GASTROEN HEPAT, V8, P645
[5]   Helicobacter pylori modulates the T helper cell 1/T helper cell 2 balance through phase-variable interaction between lipopolysaccharide and DC-SIGN [J].
Bergman, MP ;
Engering, A ;
Smits, HH ;
van Vliet, SJ ;
van Bodegraven, AA ;
Wirth, HP ;
Kapsenberg, ML ;
Vandenbroucke-Grauls, CMJE ;
van Kooyk, Y ;
Appelmelk, BJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 2004, 200 (08) :979-990
[6]  
BLASER MJ, 1995, CANCER RES, V55, P2111
[7]   Pepsinogen A, pepsinogen C, and gastrin as markers of atrophic chronic gastritis in European dyspeptics [J].
Broutet, N ;
Plebani, M ;
Sakarovitch, C ;
Sipponen, P ;
Mégraud, F .
BRITISH JOURNAL OF CANCER, 2003, 88 (08) :1239-1247
[8]   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
[9]   IMMUNE-RESPONSES TO HELICOBACTER-PYLORI IN CHILDREN WITH RECURRENT ABDOMINAL-PAIN [J].
CRABTREE, JE ;
MAHONY, MJ ;
TAYLOR, JD ;
HEATLEY, RV ;
LITTLEWOOD, JM ;
TOMPKINS, DS .
JOURNAL OF CLINICAL PATHOLOGY, 1991, 44 (09) :768-771
[10]   MUCOSAL HUMORAL IMMUNE-RESPONSE TO HELICOBACTER-PYLORI IN PATIENTS WITH DUODENITIS [J].
CRABTREE, JE ;
SHALLCROSS, TM ;
WYATT, JI ;
TAYLOR, JD ;
HEATLEY, RV ;
RATHBONE, BJ ;
LOSOWSKY, MS .
DIGESTIVE DISEASES AND SCIENCES, 1991, 36 (09) :1266-1273