Epicutaneous Immunotherapy Down-regulates the Skin Local Cytokines Production in Response To Skin Application of Peanut Protein Extract in Mice Sensitized to Peanut

2010 ◽  
Vol 135 ◽  
pp. S93
Author(s):  
Vincent Dioszeghy ◽  
Lucie Mondoulet ◽  
Veronique Dhelft ◽  
Melanie Ligouis ◽  
Emilie Puteaux ◽  
...  
JAMA ◽  
2019 ◽  
Vol 321 (10) ◽  
pp. 946 ◽  
Author(s):  
David M. Fleischer ◽  
Matthew Greenhawt ◽  
Gordon Sussman ◽  
Philippe Bégin ◽  
Anna Nowak-Wegrzyn ◽  
...  

2020 ◽  
Vol 41 (4) ◽  
pp. 278-284
Author(s):  
David M. Fleischer ◽  
Jonathan M. Spergel ◽  
Edwin H. Kim ◽  
Dianne E. Campbell ◽  
Todd D. Green ◽  
...  

Background: Epicutaneous immunotherapy is a potential novel immunotherapy that utilizes unique cutaneous immunologic properties. In a phase III, randomized, double-blind, placebo controlled clinical trial, an epicutaneous patch (DBV712) with 250 µg of peanut protein applied once daily for 12-months was statistically superior to placebo in desensitizing children with peanut allergy (ages 4‐11 years) (N = 356). Objective: To assess the relationship between the hours of daily application time and the efficacy of DBV712 250 µg. Methods: DBV712 250 µg was applied to 30 nonallergic volunteers for various durations from 2 to 24 hours and then assayed for residual peanut protein. Patch application data from the phase III clinical trial were analyzed post hoc according to prespecified responder rates and changes in the eliciting dose (ED), as measured by the geometric mean (GM) ED ratio (12 months/baseline). Results: Following application, there was a marked decrease in peanut protein on the patches from 2 to 12 hours. After 12 hours, the median peanut protein recovered was below quantification limits. The median daily patch application duration in subjects from the phase III clinical trial was 21.1 hours (DBV712 250 µg) and 22.4 hours (placebo). Ninety-five percent of the treated population achieved >10 hours per day mean application. Response rates and GM ED ratios were similar among subjects across a range of application durations; e.g., in those with a mean duration of >10 hours, the response rate was 36.6% and the GM ED ratio was 3.8, comparable with 42.6% and 4.0, respectively, in those with a mean duration of >20 hours. In DBV712 250 µg subjects with >16 hours mean application duration (84.5% of the treated population), the response rate was 38.8% versus 13.4% for placebo (difference, 24.4% [95% confidence interval, 15.5‐34.0%]; p < 0.001). Conclusion: An evaluation of residual peanut protein on patches following application and post hoc analysis of phase III data strongly suggest that allergen delivery is attained with 12‐16 hours of daily patch application time, sufficient to drive clinically meaningful desensitization to peanut after 12 months.


ISRN Allergy ◽  
2012 ◽  
Vol 2012 ◽  
pp. 1-8 ◽  
Author(s):  
Lucie Mondoulet ◽  
Vincent Dioszeghy ◽  
Mélanie Ligouis ◽  
Véronique Dhelft ◽  
Emilie Puteaux ◽  
...  

Background. The aim of this study was to compare the efficacy of epicutaneous immunotherapy (EPIT) to sublingual immunotherapy (SLIT) in a model of mice sensitized to Phleum pratense pollen. Methods. BALB/c mice were sensitized by sub-cutaneous route to pollen protein extract mixed treated for 8 weeks, using sham, EPIT, or SLIT. Measurements involved the serological response and cytokine profile from reactivated splenocytes, plethysmography after aerosol challenge to pollen, cell, and cytokine contents in the bronchoalveolar lavages (BALs). Results. After immunotherapy, sIgE was significantly decreased in the treated groups compared to sham (), whereas sIgG2a increased with EPIT and SLIT ( and versus sham). Reactivated splenocytes secreted higher levels of Th2 cytokines with sham (). Penh values were higher in sham than EPIT and SLIT. Eosinophil recruitment in BAL was significantly reduced only by EPIT (). Conclusion. In this model of mice sensitized to pollen, EPIT was at least as efficient as SLIT.


2009 ◽  
Vol 52 (3) ◽  
pp. 601-609 ◽  
Author(s):  
Gerlinde Agate Platais Brasil Teixeira ◽  
Danielle Mota Fontes Antunes ◽  
Archimedes Barbosa de Castro Júnior ◽  
Janilda Pacheco da Costa ◽  
Patrícia Olaya Paschoal ◽  
...  

Food allergy is an adverse reaction that occurs in susceptible people when they eat sensitizing foods and is one of the causes of Inflammatory Bowel Disease (IBD). The effort to understand the induction process of these diseases is important as IBD is increasing worldwide, including in Brazil. The aim of this study was to develop an experimental antigen specific inflammatory process of the gut of mice and rats, using peanut seeds. Animals were immunized with peanut protein extract before their exposure to the in natura peanut seeds. Results showed that systemic immunization with peanut protein extracts rendered significantly higher antibody titers than control groups and that immunized animals submitted to a challenge diet containing peanuts presented time dependent alterations of the gut similar to celiac disease. In conclusion, results suggested that this experimental model was a convenient tool to study the evolution of alterations in chronic antigen specific gut inflammatory process.


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