Tolerogenic Dendritic Cells Derived from Donors with Natural Rubber Latex Allergy Modulate Allergen-Specific T-Cell Responses and IgE Production
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2014Metadata
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Escobar Álvarez, Alejandro
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Tolerogenic Dendritic Cells Derived from Donors with Natural Rubber Latex Allergy Modulate Allergen-Specific T-Cell Responses and IgE Production
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Abstract
Natural rubber latex (NRL; Hevea brasiliensis) allergy is an IgE-mediated reaction to latex proteins. When latex glove exposure
is the main sensitizing agent, Hev b 5 is one of the major allergens. Dendritic cells (DC), the main antigen presenting cells,
modulated with pharmacological agents can restore tolerance in several experimental models, including allergy. In the
current study, we aimed to generate DC with tolerogenic properties from NRL-allergic patients and evaluate their ability to
modulate allergen-specific T and B cell responses. Here we show that dexamethasone-treated DC (dxDC) differentiated into
a subset of DC, characterized by low expression of MHC class II, CD40, CD80, CD86 and CD83 molecules. Compared with
LPS-matured DC, dxDC secreted lower IL-12 and higher IL-10 after CD40L activation, and induced lower alloantigenic T cell
proliferation. We also show that dxDC pulsed with the dominant Hev b 5 T-cell epitope peptide, Hev b 546–65
, inhibited both
proliferation of Hev b 5-specific T-cell lines and the production of Hev b 5-specific IgE. Additionally, dxDC induced a
subpopulation of IL-10-producing regulatory T cells that suppressed proliferation of Hev b 5-primed T cells. In conclusion,
dxDC generated from NRL-allergic patients can modulate allergen-specific T-cell responses and IgE production, supporting
their potential use in allergen-specific immunotherapy.
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This work was supported by grants from the Millennium Institute on Immunology and Immunotherapy P09-016-F, Research Support Office, Clinical
Hospital of the University of Chile, Santiago and the National Fund for Scientific and Technological Development, Chile (FONDECYT 1100102).
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URI: https://repositorio.uchile.cl/handle/2250/123584
DOI: doi:10.1371/journal.pone.0085930
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PLoS ONE 9(1): e85930. (2014)
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