%0 Journal Article %A Rodriguez, Maria J. %A Mascaraque, Ainhoa %A Ramos-Soriano, Javier %A Torres, Maria J. %A Perkins, James R. %A Gomez, Francisca %A Garrido-Arandia, Maria %A Cubells-Baeza, Nuria %A Andreu, David %A Diaz-Perales, Araceli %A Rojo, Javier %A Mayorga, Cristobalina %T Pru p 3-Epitope-based sublingual immunotherapy in a murine model for the treatment of peach allergy %D 2017 %@ 1613-4125 %U http://hdl.handle.net/10668/18616 %X Scope: Food-specific immunotherapy (SIT) is a promising treatment for lipid transfer protein (LTP)-syndrome. We propose a novel sublingual-SIT (SLIT) that combines a Pru p 3 T-cell peptide and an oligodeoxyribonucleotide (ODN) with CpG motifs (ODN-CpG) as adjuvants to induce a specific Th1/Treg response.Methods and results: LTP-peach allergic mice were treated sublingually with a combination of a CpG sequence and mono- or tetravalent systems including a Pru p 3 peptide, D-1(Prup3) or D-4(Prup3). Mice were challenged intraperitoneally with Pru p 3 one or three weeks after SLIT and tolerance was assessed.Mice treated with D-1(Prup3)+CpG were protected from anaphylaxis after Pru p 3 challenge. They showed no change in body temperature, lower levels of Pru p 3-specific IgE and IgG1 antibodies and higher levels of sIgG2a compared to the untreated group. They had fewer IgE and IgG1 secreting cells and more sIgG2a secreting cells. Moreover, a significantly lower number of Pru p 3-specific CD4(+)T cells and a higher number of Treg cells were found, alongside a Th1 cytokine pattern. These changes were maintained for three weeks after stopping treatment.Conclusion: D(1)Prup3+CpG represents a promising SIT for food allergy. It is easily synthesized and induces protection from anaphylaxis to Pru p 3 that is maintained for at least three weeks. %K Anaphylaxis %K Food-allergy %K Lipid transfer protein %K Mouse model %K Sublingual immunotherapy %K T-cell epitopes %K Food allergy %K Oral immunotherapy %K Cpg oligodeoxynucleotides %K Airway inflammation %K Dendritic cells %K Peanut %K Mice %K Mechanisms %K Sensitization %~