It is essential to distinguish the role of T lymphocytes on the physiopathology associated to more severe forms of schistosomiasis and on the immunomodulation that evolves in the majority of infected people. In this study, we generated Schistosoma mansoni-specific T cell lines and clones from patients with the acute and chronic (intestinal and hepatosplenic forms) phases of disease, from former ones, and from uninfected individuals sensitized to parasite soluble antigens. T cell lines derived from nontreated acute infected donors were capable of producing IL-4 and IL-5, while cells from treated patients secreted IFN-gamma. Lines from intestinal chronic and antigen-sensitized donors preferentially produced IFN-gamma while those from hepatosplenic patients secreted all three cytokines. The cytokine analysis of CD4(+) T cell clones revealed a Th-2/Th-0, pattern (clones producing IL-4 and IL-5 and clones producing all three cytokines) for those derived from infected patients, while cells from antigen-sensitized donors exhibited an opposite Th-1/ Th-0 pattern (clones producing IFN-gamma and clones producing all three cytokines), The possible role of these T cell populations on human schistosomiasis mansoni is discussed. (C) 1999 Academic Press.
Contigli, C., Silva-Teixeira, D.N., Del Prete, G., D'Elios, M.M., De Carli, M., Manghetti, M., et al. (1999). Phenotype and cytokine profile of Schistosoma mansoni specific T cell lines and clones derived from schistosomiasis patients with distinct clinical forms. CLINICAL IMMUNOLOGY, 91(3), 338-344 [10.1006/clim.1999.4706].
Phenotype and cytokine profile of Schistosoma mansoni specific T cell lines and clones derived from schistosomiasis patients with distinct clinical forms
D'Elios, M. M.;
1999-01-01
Abstract
It is essential to distinguish the role of T lymphocytes on the physiopathology associated to more severe forms of schistosomiasis and on the immunomodulation that evolves in the majority of infected people. In this study, we generated Schistosoma mansoni-specific T cell lines and clones from patients with the acute and chronic (intestinal and hepatosplenic forms) phases of disease, from former ones, and from uninfected individuals sensitized to parasite soluble antigens. T cell lines derived from nontreated acute infected donors were capable of producing IL-4 and IL-5, while cells from treated patients secreted IFN-gamma. Lines from intestinal chronic and antigen-sensitized donors preferentially produced IFN-gamma while those from hepatosplenic patients secreted all three cytokines. The cytokine analysis of CD4(+) T cell clones revealed a Th-2/Th-0, pattern (clones producing IL-4 and IL-5 and clones producing all three cytokines) for those derived from infected patients, while cells from antigen-sensitized donors exhibited an opposite Th-1/ Th-0 pattern (clones producing IFN-gamma and clones producing all three cytokines), The possible role of these T cell populations on human schistosomiasis mansoni is discussed. (C) 1999 Academic Press.File | Dimensione | Formato | |
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https://hdl.handle.net/11365/1220554