Peanut Allergy Clinical Trial
Official title:
Dendritic Cell Responses to Viral Stimulation in Peanut Allergic Subjects Undergoing Peanut Oral Immunotherapy
The purpose of this study is to find out if there is a way to treat children with peanut
allergy to help lower the risk of severe allergic reactions and also cause them to lose
their allergy to peanuts and to understand what happens to their immune systems when they
have viral infections while on therapy. The approach we will use to treat peanut allergy in
this study is a process called desensitization.
We think that children with a peanut allergy receiving peanut oral immunotherapy will be
able to eat more peanuts without having a reaction by the end of the study than they could
eat at the beginning. We also think that we will be able to measure changes in their immune
system and their immune system's response to viruses while they are on therapy.
Peanut allergy is known to cause severe anaphylactic reactions. Compared with other food
allergies it tends to be more persistent and also its prevalence seems to be rising.
Currently there is no proven treatment other than strict avoidance. We are attempting to
decrease the risk of anaphylaxis on accidental ingestion by desensitizing subjects to peanut
using peanut oral immunotherapy (OIT). We are also studying the effect of viral infections
on the immune system in children receiving peanut OIT.
Children ages three to sixteen years of age with peanut allergy will be given peanut OIT.
Twenty-five subjects will also be recruited as controls. These subjects will not receive any
peanut or placebo but only have skin prick testing and lab work in addition to a history and
physical exam. Active subjects will undergo a double-blind food challenge at entry to verify
that they are allergic to peanuts. If allergic, they will then have modified rush
immunotherapy on the first day and then increase the doses at least every two weeks up to a
maintenance dose of 4 grams (equivalent to about 13 peanuts). Doses will be taken daily at
home except for dose increases which will be done at Children's Medical Center. Outcome
variables of interest include response to double-blind placebo controlled food challenge,
skin prick testing, peanut specific IgE, and adverse events. These results will be compared
between the start and end of peanut OIT using appropriate statistical analysis.
;
Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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