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| ID | Type | Description | Link |
|---|---|---|---|
| NL78278.091.21 | Other Identifier | CCMO |
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| Name | Class |
|---|---|
| Wageningen University | OTHER |
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Allergic rhinitis (hay fever) can be treated successfully with allergen-specific immunotherapy (AIT) for 3-5 years. This relative expensive and prolonged treatment is not suitable for everyone and therefore it is important to predict who will benefit from this therapy early after the start of treatment.
This project will investigate whether a BAT with nasal fluid can detect inhibition during immunotherapy in comparison with a BAT with blood.
Allergic rhinitis (hay fever) can be treated successfully with allergen-specific immunotherapy (AIT) for 3-5 years. This relative expensive and prolonged treatment is not suitable for everyone and therefore it is important to predict who will benefit from this therapy early after the start of treatment. Biomarkers, like Basophil Activation Test (BAT) and IgE-facilitated allergen binding (FAB), using nasal fluid instead of blood, probably better reflect therapy effect (inhibition of an IgE-mediated allergic reaction) as the nose is the main target organ for AIT in allergic rhinitis.
This project will investigate whether a BAT with nasal fluid can detect inhibition during immunotherapy in comparison with a BAT with blood. Nasal fluid and blood samples are collected at baseline and after 8 and 16 weeks of treatment. A nasal fluid inhibition BAT is developed and validated by comparison with a BAT using serum and an IgE-FAB assay.
15 adults with birch pollen allergy, who are treated with AIT (Itulazax birch pollen tablet) and 10 adults with birch pollen allergy, who are treated with immunosuppressive medication (control group) will be included in the study.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| allergen-specific immunotherapy (AIT) | Adults with birch pollen allergy, who are treated with allergen-specific immunotherapy (AIT) |
| |
| control | Adults with birch pollen allergy, who are treated with immunosuppressive medication |
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| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| A nasal fluid Basophil Activation Test (BAT) | Other | a BAT technique for monitoring the inhibitory effect of nasal fluid on basophil activation. |
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| Measure | Description | Time Frame |
|---|---|---|
| BAT outcome nasal fluid | 8 weeks | |
| BAT outcome nasal fluid | 16 weeks | |
| BAT outcome serum | 8 weeks | |
| BAT outcome serum | 16 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| IgG4/IgA-associated inhibitory activity in nasal fluid | 8 weeks | |
| IgG4/IgA-associated inhibitory activity in nasal fluid | 16 weeks | |
| IgG4/IgA-associated inhibitory activity in serum |
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Inclusion Criteria:
Exclusion Criteria:
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Birch pollen allergic patients who are treated with Itulazax (birch pollen SLIT-tablet) and birch pollen allergic patients who are treated with immunosuppressive medication (control group).
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Janneke Ruinemans-Koerts | Contact | 0031 88 005 8888 | j.ruinemans-koerts@rijnstate.nl |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Rijnstate Hospital | Recruiting | Arnhem | 6815 AD | Netherlands |
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| ID | Term |
|---|---|
| D065631 | Rhinitis, Allergic |
| ID | Term |
|---|---|
| D012220 | Rhinitis |
| D009668 | Nose Diseases |
| D012140 | Respiratory Tract Diseases |
| D012130 | Respiratory Hypersensitivity |
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| 8 weeks |
| IgG4/IgA-associated inhibitory activity in serum | 16 weeks |
| D010038 |
| Otorhinolaryngologic Diseases |
| D006969 | Hypersensitivity, Immediate |
| D006967 | Hypersensitivity |
| D007154 | Immune System Diseases |