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- W1636854345 abstract "Regulatory T cells (Tregs) are physiologically designed to prevent autoimmune disease and maintain self-tolerance. In tumour microenvironments, their presence is related to a poor prognosis, and they influence the therapeutic outcome due to their capacity to suppress the immune response by cell-cell contact and to release immunosuppressive cytokines. In this study, we demonstrate that Treg immunosuppressive activity can be modulated by the cross-linking between the CD45RA expressed by Tregs and the C-type lectin MGL. This specific interaction strongly decreases the im-munosuppressive activity of Tregs, restoring the proliferative capacity of co-cultured T lymphocytes. This effect can be attributed to changes in CD45RA and TCR signalling through the inhibition of Lck and inactivation of Zap-70, an increase in the Foxp3 methylation status and, ultimately, the reduced production of suppressive cytokines. These results indicate a role of MGL as an immunomodulator within the tumour microenvironment interfering with Treg functions, suggesting its possible use in the design of anticancer vaccines." @default.
- W1636854345 created "2016-06-24" @default.
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- W1636854345 date "2015-07-06" @default.
- W1636854345 modified "2023-10-02" @default.
- W1636854345 title "The Macrophage Galactose-Type C-Type Lectin (MGL) Modulates Regulatory T Cell Functions" @default.
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- W1636854345 doi "https://doi.org/10.1371/journal.pone.0132617" @default.
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