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. 2001 Oct;49(4):512–518. doi: 10.1136/gut.49.4.512

Human gastric B cell responses can be induced by intestinal immunisation

M Quiding-Jarbrink 1, H Lonroth 1, I Ahlstedt 1, J Holmgren 1, A Svennerholm 1
PMCID: PMC1728478  PMID: 11559648

Abstract

BACKGROUND—In a previous study, we found that oral vaccination induces strong B cell responses in the stomach of Helicobacter pylori infected but not of uninfected individuals. In this study, we have evaluated the possibility of inducing gastric immune responses in H pylori infected volunteers by intestinal and gastric immunisation.
METHODSH pylori infected subjects were given two doses of an inactivated cholera vaccine, either intestinally via an endoscope approximately 30 cm distal to the pylorus sphincter or intragastrically as small droplets applied directly onto the stomach mucosa. Uninfected individuals received the vaccine by standard oral procedure. Vaccine specific antibody secreting cells in antral and duodenal biopsies were detected by the enzyme linked immunospot assay technique before and seven days after the second immunisation.
RESULTS—Intestinal immunisations resulted in induction of vaccine specific gastric IgA secreting cells in five of eight volunteers. This immunisation schedule also gave rise to specific duodenal antibody secreting cells in seven of eight individuals. Local gastric immunisation resulted in the induction of specific B cells in the gastric mucosa of four of eight volunteers. Gastric antigen application also resulted in B cell responses in the duodenum in all volunteers. Uninfected volunteers receiving the vaccine perorally responded in the duodenum but not in the stomach.
CONCLUSIONSH pylori infection increases the ability of the gastric mucosa to serve as an expression site for intestinally induced B cell responses. These findings are of importance when designing a therapeutic H pylori vaccine, and based on our results such a vaccine can be delivered along the whole upper gastrointestinal tract.


Keywords: Helicobacter pylori; vaccine; stomach; B cell; lymphocyte trafficking

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Figure 1  .

Figure 1  

Duodenal antibody secreting cell (ASC) responses after intestinal, intragastric, or peroral immunisations. Duodenal biopsies were collected one week before and one week after a second immunisation with cholera vaccine, and IgA secreting ASC reacting with cholera toxin B subunit (CTB) were detected by ELISPOT assays. Data are presented as individual frequencies of CTB specific IgA secreting cells per 104 total IgA secreting cells before (Pre) and after (Post) the respective immunisation regimens. Horizontal lines represent arithmetic mean. Numbers indicate the frequencies of responders in the respective groups.

Figure 2  .

Figure 2  

Gastric antibody secreting cell (ASC) responses after intestinal or intragastric immunisations. Gastric biopsies were collected one week before and one week after a second immunisation with cholera vaccine, and ASC reacting with cholera toxin B subunit (CTB) were detected by ELISPOT assays. Data are presented as individual frequencies of CTB specific IgA secreting cells per 104 total IgA secreting cells before (Pre) and after (Post) the respective immunisation regimens. Horizontal lines represent arithmetic mean. One individual had very high levels of CTB reactive ASC at the first examination but only background levels after immunisation. However, as this subject had equally high levels of BSA reactive ASC before immunisation, the ASC observed in the preimmunisation specimen most likely represented non-specific reactions and hence data from this individual were not incorporated. Numbers indicate the frequencies of responders in the respective groups.

Figure 3  .

Figure 3  

Circulating antibody secreting cell (ASC) responses after intestinal, intragastric, or peroral immunisation. Venous blood was collected before and after immunisation via the indicated routes and was analysed for the presence of cholera toxin B subunit (CTB) specific ASC in ELISPOT assays. Data are presented as individual frequencies of CTB specific IgG and IgA secreting cells before and after the respective immunisation regimens. Horizontal lines represent arithmetic mean. Numbers indicate the frequencies of responders in the respective groups. Vaccine specific ASC could not be detected before immunisation in any of the volunteers.

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