LuLISA: Feasibility Study of a New Immunoglobulin E (IgE) Assay Method
Study Details
Study Description
Brief Summary
The main objective is to study the feasibility of a new specific IgE assay using a bioluminescence technique in a pediatric and adult allergic population. For this, we will collect blood, and urine during a blood test scheduled for the follow-up of the patient.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Detailed Description
Allergy is a raising public health problem. Specific IgE assays are useful tools to investigate the physiopathology of allergies. This method is achieved mainly by the ImmunoCAP enzyme immunoassay technique. This is an expensive test that requires a significant amount of blood. This is a limitation particularly in children. The time to get the results is long and a second consultation has to be scheduled in order to communicate the results to the patients. The main objective of this study is to assess the feasibility of a new specific IgE assay, named LuLISA, using a bioluminescence technique in urine and blood samples from pediatric and adult allergic population. This technique was recently published for the quantification of IgE against two peanut allergens and needs to be extended for the detection of other major allergens. A secondary objective is the evaluation of the time needed to obtain results.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| People with sensitization or allergy blood and urine will be collected during a blood test scheduled for the follow-up of the patient |
Biological: collection of blood and urine
blood and urine will be collected during a blood test scheduled for the follow-up of the patient
|
Outcome Measures
Primary Outcome Measures
- Estimation of the the correlation of specific IgE concentrations for a given allergen analyzed using two different methods [Day 0]
specific IgE concentrations for a given allergen will be measured by both LuLISA and ImmunoCAP and the results will be compared
Secondary Outcome Measures
- To study the correlation between the results of specific serum and urinary IgE dosages by LuLISA [Day 0]
specific IgE concentrations for a given allergen will be measured in the sera and the urine from the same patient and the results will be compared
- To study the correlation between the results of specific IgE dosages in the venous blood and the capillary blood [Day 0]
specific IgE concentrations for a given allergen will be measured in the venous blood and the capillary blood from the same patient and the results will be compared
Eligibility Criteria
Criteria
Inclusion Criteria:
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Males or females 6 months' old or older
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Sensitization or allergy towards a trophallergen, an aeroallergen, hymenoptera venom or drug proven by:
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positive skin test (s)
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and / or IgE specific (s)> 0.1 kUA / L
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and / or anamnesis in favor of an allergic reaction of mediated IgE
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Social coverage up to date
Exclusion Criteria:
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Children younger than 6 months'old
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Children's weight less than 10 kg
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Pregnant or breastfeeding women
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Patients with cystic fibrosis
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Patients with dysimmune or autoimmune pathology
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Anamnesis in favor of a delayed allergy or a contact allergy.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | University Hospital | Toulouse | France | 31000 | |
| 2 | Larrey hospital | Toulouse | France | 31059 |
Sponsors and Collaborators
- University Hospital, Toulouse
Investigators
- Principal Investigator: Marine Michelet, MD, University Hospital, Toulouse
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- RC31/20/0293