부산대학교 도서관

Animal studies define CD4+ CD25+ T cells as a subset that protect against autoimmune inflammation. We wanted to investigate whether CD4+ CD25+ T cells from patients with recurrent tonsillitis could suppress the proliferation of other tonsil cells, in vitro , as this immunological tissue also may serve as a model for chronic inflammation. Tonsil CD4+ CD25+ cells markedly suppressed the proliferation of CD4+ CD25– T cells in Concanavalin A-stimulated cocultures compared with cultures containing CD4+ CD25– T cells only. The suppression exerted by the CD4+ CD25+ cells was abrogated if these cells were irradiated before coculture or if interleukin (IL)-2 was added to the culture medium. CD4+ CD25+ T cells proliferated poorly in response to mitogen, when cultured alone. Substitution with CD4+ CD25+ T cells isolated from peripheral blood, enriched by similar methods, did not downregulate the proliferation of CD4+ CD25– responder cells from tonsils. The augmented suppressive ability of tonsil CD4+ CD25+ T cells compared with cells of this phenotype from blood, on CD4+ CD25– responder cells from tonsils, suggests that there may be a functional difference between CD25+ cells from the two locations. In conclusion, CD4+ CD25+ T cells from inflamed tonsils distinctly suppressed T-cell responses to mitogen in vitro , pointing to a regulatory role for CD4+ CD25+ cells retrieved from inflammatory reactions in humans. [ABSTRACT FROM AUTHOR]