The immunological mechanisms involved in the development of
duodenal ulcer, especially in childhood, are unclear. Helicobacter pylori-positive children and adults, with and without
duodenal ulcer, were therefore compared with respect to CD4(+) T-cells, and CD8(+) T-cells, B-cells and B1a-cells, as well as cell activation (CD4(+)/
HLA-DR(+) and CD8(+)/
HLA-DR(+)) and co-stimulatory (CD4(+)/CD28(+) and CD8(+)/CD28(+)) markers, in peripheral blood. Children with and without
duodenal ulcer differed significantly. In particular, there was a phenotypic change in CD8(+) T-cells from children with
ulcer that involved a 200% increase in the number of CD8(+)/
HLA-DR(+) cells/mm(3) and a decrease of 34.2% in the number of CD8(+)/CD28(+) cells/mm(3). This phenotype of chronically activated memory CD8(+) T-cells, which has also been observed in patients with
AIDS and
tuberculosis, is associated with disease severity and progression. A lower frequency of B1a-cells was also observed in the group of children with
ulcer. Conversely, no difference between infected adults with and without
ulcer was observed, but the percentage of CD4(+)/
HLA-DR(+) cells was lower in adults with
ulcer, suggesting that a down-regulated immune response may play a role in the development of
duodenal ulcer in adults. Gastric
inflammation correlated positively with CD4(+) and chronically activated CD4(+) T-cells in children and adults without
duodenal ulcer, respectively. These results suggest that there are differences in the immunophenotyping profile between H. pylori-positive children and adults with
duodenal ulcer, indicating the possibility of distinct immune mechanisms in the development of the disease according to age.