Tolerogenic Dendritic Cells Derived from Donors with Natural Rubber Latex Allergy Modulate Allergen-Specific T-Cell Responses and IgE Production

被引:24
作者
Escobar, Alejandro [1 ]
Aguirre, Adam [2 ]
Guzman, Maria Antonieta [3 ]
Gonzalez, Rodrigo [4 ]
Catalan, Diego [5 ]
Acuna-Castillo, Claudio [6 ]
Larrondo, Milton [4 ]
Lopez, Mercedes [5 ]
Pesce, Barbara [5 ]
Rolland, Jennifer [7 ]
O'Hehir, Robyn [7 ]
Aguillon, Juan Carlos [5 ]
机构
[1] Univ Chile, Fac Dent, Res Inst Dent Sci, Santiago, Chile
[2] Catholic Univ Chile, Fac Chem, Dept Pharm, Santiago, Chile
[3] Univ Chile, Clin Hosp Univ Chile, Allergy Ctr, Santiago, Chile
[4] Univ Chile, Blood Bank Clin Hosp Univ Chile, Santiago, Chile
[5] Univ Chile, Millennium Inst Immunol & Immunotherapy, Fac Med, Program Immunol, Santiago, Chile
[6] Univ Santiago, Fac Chem & Biol, Dept Biol, Santiago, Chile
[7] Monash Univ, AMREP, Dept Immunol, Melbourne, Vic 3004, Australia
来源
PLOS ONE | 2014年 / 9卷 / 01期
关键词
HEALTH-CARE WORKERS; GRASS-POLLEN IMMUNOTHERAPY; HEV B 5; INTERLEUKIN-10; PRODUCTION; VENOM IMMUNOTHERAPY; IMMUNE-RESPONSES; REGULATORY CELLS; IN-VIVO; ANTIGEN; DIFFERENTIATION;
D O I
10.1371/journal.pone.0085930
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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 5(46-65), 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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页数:10
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