NONOPSONIC ACTIVATION OF NEUTROPHILS AND CYTOTOXIN PRODUCTION BY HELICOBACTER-PYLORI - ULCEROGENIC MARKERS

被引:51
作者
RAUTELIN, H
BLOMBERG, B
JARNEROT, G
DANIELSSON, D
机构
[1] OREBRO MED CTR HOSP,DEPT CLIN MICROBIOL & IMMUNOL,S-70185 OREBRO,SWEDEN
[2] UNIV HELSINKI,DEPT BACTERIOL & IMMUNOL,HELSINKI,FINLAND
[3] OREBRO MED CTR HOSP,DEPT INTERNAL MED,DIV GASTROENTEROL,OREBRO,SWEDEN
关键词
CHEMILUMINESCENCE; CYTOTOXIN; HELA CELLS; HELICOBACTER PYLORI; NONOPSONIC ACTIVATION OF NEUTROPHILS; PEPTIC ULCER DISEASE;
D O I
10.3109/00365529409090450
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Fifty-four clinical isolates of Helicobacter pylori from human gastric biopsy specimens were tested for cytotoxin production, as determined by intracellular vacuolization of HeLa cells, and for the induction of oxidative burst in human polymorphonuclear leukocytes (PMNLs), as measured by luminol-enhanced chemiluminescence (CL). Nonopsonized, 20 of the H. pylori strains induced a rapid and strong CL response, in contrast to 30 other strains, which showed only weak and slow responses. Another four strains gave inconclusive results. Cytotoxin production was demonstrated in 10 of the 20 strains with rapid responses but only in 3 of the 30 strains with slow and low responses (p = 0.0027, Fisher's exact test, two-tailed). Eleven of the 15 cytotoxin-producing strains (p = 0.0135) and 13 of the 20 strains with strong CL responses (p = 0.0209) were from 22 patients with peptic ulcer disease (PUD). The ability of some nonopsonized H. pylori to activate PMNLs showed co-variation with their ability to produce cytotoxin, but these two properties seem to be independent markers of PUD.
引用
收藏
页码:128 / 132
页数:5
相关论文
共 28 条
[1]   OXYGEN-DEPENDENT MICROBIAL KILLING BY PHAGOCYTES .1. [J].
BABIOR, BM .
NEW ENGLAND JOURNAL OF MEDICINE, 1978, 298 (12) :659-668
[2]   INTERACTION OF CAMPYLOBACTER SPECIES WITH ANTIBODY, COMPLEMENT AND PHAGOCYTES [J].
BERNATOWSKA, E ;
JOSE, P ;
DAVIES, H ;
STEPHENSON, M ;
WEBSTER, D .
GUT, 1989, 30 (07) :906-911
[3]   HELICOBACTER-PYLORI AND THE PATHOGENESIS OF GASTRODUODENAL INFLAMMATION [J].
BLASER, MJ .
JOURNAL OF INFECTIOUS DISEASES, 1990, 161 (04) :626-633
[4]   PREVALENCE OF CAMPYLOBACTER-PYLORI IN AN UNSELECTED SWEDISH POPULATION OF PATIENTS REFERRED FOR GASTROSCOPY [J].
BLOMBERG, B ;
JARNEROT, G ;
KJELLANDER, J ;
DANIELSSON, D ;
KRAAZ, W .
SCANDINAVIAN JOURNAL OF GASTROENTEROLOGY, 1988, 23 (03) :358-362
[5]  
BOYUM A, 1974, TISSUE ANTIGENS, V4, P269
[6]  
BRIHEIM G, 1984, INFECT IMMUN, V45, P1
[7]   CHARACTERIZATION OF AND HUMAN SEROLOGIC RESPONSE TO PROTEINS IN HELICOBACTER-PYLORI BROTH CULTURE SUPERNATANTS WITH VACUOLIZING CYTOTOXIN ACTIVITY [J].
COVER, TL ;
DOOLEY, CP ;
BLASER, MJ .
INFECTION AND IMMUNITY, 1990, 58 (03) :603-610
[8]   EXPRESSION OF 120 KILODALTON PROTEIN AND CYTOTOXICITY IN HELICOBACTER-PYLORI [J].
CRABTREE, JE ;
FIGURA, N ;
TAYLOR, JD ;
BUGNOLI, M ;
ARMELLINI, D ;
TOMPKINS, DS .
JOURNAL OF CLINICAL PATHOLOGY, 1992, 45 (08) :733-734
[9]   MUCOSAL REACTIVE OXYGEN METABOLITE PRODUCTION IN DUODENAL-ULCER DISEASE [J].
DAVIES, GR ;
SIMMONDS, NJ ;
STEVENS, TRJ ;
GRANDISON, A ;
BLAKE, DR ;
RAMPTON, DS .
GUT, 1992, 33 (11) :1467-1472
[10]   CAMPYLOBACTER-PYLORI VIRULENCE FACTORS IN GNOTOBIOTIC PIGLETS [J].
EATON, KA ;
MORGAN, DR ;
KRAKOWKA, S .
INFECTION AND IMMUNITY, 1989, 57 (04) :1119-1125