Induction of B cell responses in the stomach of Helicobacter pylori-infected subjects after oral cholera vaccination

被引:73
作者
Mattsson, A
Lönroth, H
Quiding-Järbrink, M
Svennerholm, AM
机构
[1] Gothenburg Univ, Dept Med Microbiol & Immunol, S-41346 Gothenburg, Sweden
[2] Gothenburg Univ, Dept Surg, S-41346 Gothenburg, Sweden
关键词
antibody secreting cells; ELISPOT; human; antrum; mucosa;
D O I
10.1172/JCI22
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
We have evaluated the possibility of inducing antibody responses locally in the human stomach as a prerequisite for the development of a vaccine against Helicobacter pylori, Both H. pylori-infected and noninfected subjects were immunized with an oral B subunit whole cell(BS-WC) cholera vaccine, and total and vaccine-specific antibody-secreting cells (ASC) were determined by the enzyme-linked immunospot (ELISPOT) technique in cells isolated from the antrum and duodenum, respectively, before and after vaccination. Most of the subjects responded to the vaccination with high frequencies of vaccine-specific ASCs in the duodenum as well as high-serum antibody titers, and no significant differences were seen in the responses between H, pylori-infected and noninfected subjects. When studying the gastric mucosa, on the other hand, there were dramatic differences between the H. pylori-infected and the noninfected subjects. Thus, whereas none of the noninfected subjects responded to the immunization in antrum, most of the H, pylori-infected subjects had high frequencies of vaccine-specific ASCs in this location after vaccination. Furthermore, the H, pylori-infected subjects had strikingly higher (as a mean 80-fold) frequencies of total IgA-secreting cells in antrum than the noninfected subjects, whereas the frequencies of total IgA-secreting cells in the duodenum were comparable between the groups. In conclusion, these results demonstrate the possibility of inducing antibody responses locally in the gastric mucosa of H, pylori-infected individuals, a finding with obvious implications for the future development of a therapeutic vaccine against H, pylori.
引用
收藏
页码:51 / 56
页数:6
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