Immunologic Profile of Children With Severe Allergies to Peanuts and Nuts After Induction of Tolerance

NCT01996774 | Completed

• 1 other identifier: RC-P0013
• Study Type: observational
• Target: 70
• Locations: 1 country
• Sites: 1

Brief Summary

Many authors propose the strict avoidance of allergenic food as the only treatment for children known to be allergic to certain food. However, it has been observed an increase of the frequency and severity of the allergic accidents in these children in the long term. Other teams have suggested treating these allergies (in particular peanut allergies) by controlled and progressive reintroduction of the allergenic food. A good tolerance and a prevention of allergic reactions consecutive to the ingestion of the same allergenic food were observed. The immunological mechanisms of this type of treatment are not well known. A decrease of specific IgE and an increase of IgG4 have been observed in the case of egg allergies after this kind of treatment. Certain experiments realized in mice models testing the allergenic stimulation challenge showed an increase of lymphocytes T regulators (foxp3+ , CD4+, CD25+), stimulated by dendritic cells, and also an increase of interleukin 10, leading to the modification of the balance between Th1 and Th2.Our hypothesis is that after treating allergies by the reintroduction of the allergenic food, the immunological mechanism of acquisition of tolerance is associated to variations in populations of lymphocytes and in the activation or decrease of pro and anti-inflammatory cytokines. This reaction will be studied in two groups: 1. Children with a confirmed allergy to peanuts or nuts and 2. Children without antecedents of allergy or familiar atopy.

Conditions

Immune Tolerance

Outcome Measures

Primary Outcomes (1)

• Allergen-specific biomarkers in blood and saliva

  within the 15 days of subject enrollment

Study Arms (3)

Child, peanut/ nut allergy, no treatment

Child, peanut/nut allergy, tolerance

Non allergic child, without atopia

Eligibility Criteria

• Age: 1 Year - 17 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Child (0-17)
• Sampling Method: Probability Sample

Study Population

Children with allergy to peanuts and nuts hospitalized for initial diagnosis or for treatment in the Allergology Center of GHICL.

You may qualify if:

• Children (between 1 and 16 years old)known to have an allergy to peanuts and nuts detected by specific IgE, specific recombinant rArah (1 to 8) and R Cora and other allergens with a value superior or equal to 5KU/L.
• Child, parents or legal representatives have given informed consent to participate in the study after being informed in details about the protocol.

You may not qualify if:

• Immunodeficiency,
• Children or parents in disagreement with the study
• Children without standard diagnostic test at recruitment (oral provocation test vs. placebo)
• Children who reacted to placebo
• Children with uncontrolled asthma or respiratory disease
• Treatment with oral antihistaminic or corticoids one week before
• Neither Healthcare coverage nor insurance
• Group 2:
• Children (between 1 and 16 years old)known to have an allergy to peanuts and nuts detected by specific IgE, specific recombinant rArah (1 to 8) and R Cora and other allergens with a value superior or equal to 5KU/L
• Doubling the values of the threshold after second oral challenge compared to the tests of reference
• Child, parents or legal representatives have given informed consent to participate in the study after being informed in details about the protocol.
• Immunodeficiency,
• Children or parents in disagreement with the study
• Children without standard diagnostic test at recruitment (oral provocation test vs placebo)
• Children who reacted to placebo

Sponsors & Collaborators

• Lille Catholic University: lead

Study Sites (1)

Groupement des Hôpitaux de l'Institut Catholique de Lille

Lomme, Nord, 59462, France

Location

Biospecimen

Retention: SAMPLES WITHOUT DNA

Blood, serum, saliva

Study Officials

• Catalina ILIESCU, MD, PhD

  Direction de la Recherche Médicale, Groupement des Hôpitaux de l'Institut Catholique de Lille

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: observational
• Observational Model: CASE CONTROL
• Time Perspective: CROSS SECTIONAL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: November 22, 2013
• First Posted: November 27, 2013
• Study Start: February 1, 2012
• Primary Completion: March 1, 2014
• Study Completion: March 1, 2014
• Last Updated: August 19, 2014

Record last verified: 2014-08

Locations

FR (1)