Δημοσίευση

Vaccination with Trichinella spirallis antigens increases CD8+ peripheral T cells and enhances the Th2 immune response in Leishmania infantum challenged mice.

ΤίτλοςVaccination with Trichinella spirallis antigens increases CD8+ peripheral T cells and enhances the Th2 immune response in Leishmania infantum challenged mice.
Publication TypeJournal Article
Year of Publication2009
AuthorsDaoudaki, M., Diakou A., Frydas S., Fouzas I., Karagouni E., Vavatsi N., & Haralabidis S.
JournalInt J Immunopathol Pharmacol
Volume22
Issue1
Pagination169-74
Date Published2009 Jan-Mar
ISSN0394-6320
Λέξεις κλειδιάAnimals, Antibodies, Protozoan, Antigens, Helminth, CD8-Positive T-Lymphocytes, Female, Immunoglobulin G, Leishmania infantum, Leishmaniasis, Visceral, Mice, Mice, Inbred BALB C, Th2 Cells, Trichinella spiralis, Vaccination
Abstract

In this study we investigate the effect of Trichinella spiralis vaccination on immune responses elicited in BALB/c mice challenged subcutaneously with 0.5 x 10 6 of Leishmania infantum promastigotes. Secretion of specific anti-L. infantum antibodies and changes in the number of CD4+, CD8+ T cell and CD19+ B cells in the peripheral blood were tested for the evaluation of immune responses. Immunization with low amounts of T. spiralis antigens induced depression in anti-Leishmania specific antibodies of the IgG1 isotype, while no changes in the number of CD4+ and CD8+ T cell subpopulations or CD19+ B cells were observed. In contrast, high amounts of T. spiralis antigens induced an enhancement in anti-Leishmania specific antibodies of total IgG and IgG1 isotype, increase of CD8+ T cell number and activation of CD19+ B cells, indicated by the co-expression of CD69 marker. Our results suggest that immunization with a certain dose of T. spiralis antigens in experimentally challenged mice with L. infantum leads to an increase of peripheral CD8+ T cells which are responsible for the control of L. infantum infection, although a simultaneous enhancement in Th2-type of immune response is also observed.

Alternate JournalInt J Immunopathol Pharmacol
PubMed ID19309564

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