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

Immune Tolerance Clinical Trial

— TOY  

Official title:

Immunologic Profile of Children and Teenagers With Severe Allergy to Peanuts and Nuts After Induction of Tolerance: a Pilot Project

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01996774
• Other study ID #: RC-P0013
• Status: Completed
• Phase: N/A
• First received: November 22, 2013
• Last updated: August 18, 2014
• Start date: February 2012
• Est. completion date: March 2014

Study information

• Verified date: August 2014
• Source: Lille Catholic University
• Contact: n/a
• Is FDA regulated: No
• Health authority: France: Ministry of Health
• Study type: Observational

Clinical Trial 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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 70
• Est. completion date: March 2014
• Est. primary completion date: March 2014
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 1 Year to 17 Years

Eligibility

Group 1:

Inclusion Criteria:

• 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.

Exclusion Criteria:

• 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:

Inclusion criteria

• 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.

Exclusion Criteria:

• 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 3:

Inclusion criteria:

• Children (between 1 and 16 years old)

• No allergy to peanuts or nuts

• No antecedents of atopia

• Child, parents or legal representatives have given informed consent to participate in the study after being informed in details about the protocol

Exclusion Criteria:

• 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

Study Design

Observational Model: Case Control, Time Perspective: Cross-Sectional

Related Conditions & MeSH terms

• Immune Tolerance
• Peanut Hypersensitivity

Locations

Country	Name	City	State
France	Groupement des Hôpitaux de l'Institut Catholique de Lille	Lomme	Nord

Sponsors (1)

Lead Sponsor	Collaborator
Lille Catholic University

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Allergen-specific biomarkers in blood and saliva		within the 15 days of subject enrollment	No