Serological response to Helicobacter pylori recombinant antigens in Chilean infected patients with duodenal ulcer, non-ulcer dyspepsia and gastric cancer

被引:13
作者
Opazo, P
Müller, I
Rollán, A
Valenzuela, P
Yudelevich, A
García-de la Guarda, R
Urra, S
Venegas, A
机构
[1] Bios Chile Ingn Genet SA, Unidad Biol MOl, Santiago, Chile
[2] Pontificia Univ Catolica Chile, Fac Ciencias Biol, Dept Mol Genet & Microbiol, Santiago, Chile
关键词
Helicobacter pylori; CagA; VacA; H-pylori-cloned antigens; sera antibodies;
D O I
10.1111/j.1699-0463.1999.tb01510.x
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We have previously cloned 10 Helicobacter pylori antigen genes from a Chilean strain including: cytotoxin VacA, a truncated region of CagA (called A17), a species-specific protein (Ag26), urease subunits (UreA, UreB), a flagellin, (FlaB), heat shock proteins (HspA and HspB), an adhesin (HpaA) and a lipoprotein (Lpp20). Immunogenicity of these antigens was tested by immunoblot with sera of Chilean infected patients, revealing that HpaA, A17, HspB and VacA were more frequently recognized (86%, 820/o, 68% and 68%, respectively). According to the clinical condition, it was determined that Lpp20 was preferentially recognized by sera from non-ulcer dyspepsia patients (80%), A17 and VacA by patients with duodenal ulcer (92% and 83% respectively), and HspB by patients with duodenal ulcer (83%) and gastric cancer (90%). An ELISA was developed with a purified mixture of A17 and VacA antigens to test the different groups of patients. It was found that sera from duodenal ulcer patients showed higher values than those from non-ulcer dyspepsia patients, but this difference was not significant (p<0.2). Moreover, sera from gastric cancer patients showed values lower than those from non-ulcer dyspepsia patients (p<0.019). These results indicate that, in the Chilean population, antibodies raised against VacA and A17 are not markers either for duodenal ulcer or for gastric cancer.
引用
收藏
页码:1069 / 1078
页数:10
相关论文
共 57 条
  • [41] 135::AID-IJC1&gt
  • [42] 3.0.CO
  • [43] 2-#
  • [44] GENETIC-ANALYSIS OF THE HELICOBACTER-PYLORI VACUOLATING CYTOTOXIN - STRUCTURAL SIMILARITIES WITH THE IGA PROTEASE TYPE OF EXPORTED PROTEIN
    SCHMITT, W
    HAAS, R
    [J]. MOLECULAR MICROBIOLOGY, 1994, 12 (02) : 307 - 319
  • [45] HELICOBACTER-PYLORI INFECTION-RATES IN RELATION TO AGE AND SOCIAL-CLASS IN A POPULATION OF WELSH MEN
    SITAS, F
    FORMAN, D
    YARNELL, JWG
    BURR, ML
    ELWOOD, PC
    PEDLEY, S
    MARKS, KJ
    [J]. GUT, 1991, 32 (01) : 25 - 28
  • [46] HELICOBACTER-PYLORI HSPA-HSPB HEAT-SHOCK GENE-CLUSTER - NUCLEOTIDE-SEQUENCE, EXPRESSION, PUTATIVE FUNCTION AND IMMUNOGENICITY
    SUERBAUM, S
    THIBERGE, JM
    KANSAU, I
    FERRERO, RL
    LABIGNE, A
    [J]. MOLECULAR MICROBIOLOGY, 1994, 14 (05) : 959 - 974
  • [47] CLONING AND GENETIC-CHARACTERIZATION OF THE HELICOBACTER-PYLORI AND HELICOBACTER-MUSTELAE FLAB FLAGELLIN GENES AND CONSTRUCTION OF HELICOBACTER-PYLORI FLAA-NEGATIVE AND FLAB-NEGATIVE MUTANTS BY ELECTROPORATION-MEDIATED ALLELIC EXCHANGE
    SUERBAUM, S
    JOSENHANS, C
    LABIGNE, A
    [J]. JOURNAL OF BACTERIOLOGY, 1993, 175 (11) : 3278 - 3288
  • [48] Torres J, 1998, INT J CANCER, V78, P298, DOI 10.1002/(SICI)1097-0215(19981029)78:3&lt
  • [49] 298::AID-IJC6&gt
  • [50] 3.0.CO