Immunological Comparison of AIT and SCIT Immunotherapy Against Grass Pollen
Primary Purpose
Allergic Rhinitis Due to Grass Pollens
Status
Completed
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
ALK Grazax 75,000 SQ-T "Phleum pratense"
ALK AluTard 225 "Phleum pratense"
Sponsored by
About this trial
This is an interventional basic science trial for Allergic Rhinitis Due to Grass Pollens
Eligibility Criteria
Inclusion Criteria:
- history of rhinitis with hay fever symptoms during the grass pollen season,
- a skin-prick-test-verified grass pollen allergy (Phleum pratense),
- eligibility for immunotherapy based on ARIA guidelines
Exclusion Criteria:
- current long-term systemic steroid treatment,
- previous immunotherapy,
- asthma and outside-season airway hyperresponsiveness (AHR) (September 2011),
- pregnancy,
- negative RAST for grass, and
- treatment side effect
Sites / Locations
- Bispebjerg University Hospital
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
No Intervention
Active Comparator
Active Comparator
Arm Label
Control group
Subcutaneous Immunotherapy (SCIT)
Sublingual Allergen Immunotherapy Tablets (AIT)
Arm Description
Treatment using ALK AluTard 225 "Phleum pratense"
Treatment using ALK Grazax 75,000 SQ-T "Phleum pratense"
Outcomes
Primary Outcome Measures
Changes over time in specific Antibodies
IgE, IgG4
Changes over time in Basophil Activation Test
Secondary Outcome Measures
Changes over time in Nasal Challenge symptoms
Full Information
NCT ID
NCT01889875
First Posted
June 24, 2013
Last Updated
June 26, 2013
Sponsor
Bispebjerg Hospital
Collaborators
ALK-Abelló A/S
1. Study Identification
Unique Protocol Identification Number
NCT01889875
Brief Title
Immunological Comparison of AIT and SCIT Immunotherapy Against Grass Pollen
Official Title
Immunological Comparison of AIT and SCIT Immunotherapy Against Grass Pollen
Study Type
Interventional
2. Study Status
Record Verification Date
June 2013
Overall Recruitment Status
Completed
Study Start Date
November 2010 (undefined)
Primary Completion Date
August 2012 (Actual)
Study Completion Date
August 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Bispebjerg Hospital
Collaborators
ALK-Abelló A/S
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
Treatment of pollen allergies can be roughly divided into symptomatic treatment (e.g. antihistamines, steroids) and potentially curative immunotherapy. Immunotherapy can be delivered using subcutaneous or oral (mucosal) routes, with similar clinical outcome. The study seeks to compare immunological changes during subcutaneous (SCIT) and sublingual tablet (AIT) immunotherapy of grass pollen allergy (hayfever).
Detailed Description
Worldwide, more than 400 million people have allergic rhinitis, and sick-leave due to this condition costs societies billions of dollars annually1. Allergic rhinitis is most commonly treated with oral antihistamines and intranasal corticosteroids2. For moderate-severe rhinitis with poor control on topical treatment, immunotherapy should be considered3. Allergen immunotherapy is the only disease-modifying treatment available for IgE mediated allergy.
Immunotherapy is most commonly administered with subcutaneous injections of SQ-standardized allergen extracts (SCIT) and to a lesser extent, as sublingual drops (SLIT). However, other options now exist with the newly developed sublingual allergen immunotherapy tablets (AIT). The clinical effect of AIT4 and SCIT5 against grass pollen allergy has been demonstrated in large double-blind-placebo-controlled registration trials. These studies report significant reductions of symptom scores (AIT 30%, SCIT 32%) and seasonal rescue medication scores (AIT 38%, SCIT 41%) when compared with placebo4,5, persisting several years after withdrawal4,6. Immunotherapy may prevent new sensitizations and progression of rhinitis to asthma7-11. Allergen immunotherapy is generally well tolerated with few side effects, although a potential risk of anaphylactic reactions exists 12. A review of recent parallel meta-analyses on immunotherapy for grass pollen rhinitis suggests that the safety profile of AIT is superior to that of SCIT13.
The recommended length of immunotherapy with both SCIT and AIT is 3-5 years2, although the route of administration and the doses of allergen differ substantially. SCIT involves an up-dosing phase lasting 12-15 weeks with one or more weekly injections of increasing doses of allergen followed by a maintenance dose every 6-10 weeks. AIT starts with the daily maintenance dose, resulting in high cumulative doses. It is largely unknown whether the immunological mechanisms involved in the clinical effect are the same.
The changes in immunology have been extensively investigated for SCIT, and the most pronounced patterns are: 1) the induction of blocking antibodies, 2) a shift in Th1/Th2 balance towards Th1, and 3) induction of regulatory T cells. Similar mechanisms seem to be in play for AIT 14-16. Increases in allergen-specific non-IgE antibodies have been demonstrated in large trials of both SCIT and AIT treatment17,18, and studies have demonstrated that serum antibodies can reduce in vitro reactions mimicking allergic responses, such as IgE binding to allergen, IgE facilitated antigen presentation and basophil activation19-22, suggesting that both humoral and cellular effects play a role23.
The aim of the present study was to compare the effect of AIT and SCIT on antibody titers (IgE and IgG4), on allergen-IgE interaction in competition assays (IgE-blocking factor and FAP inhibition) and on effector cell activation (BAT). Nasal challenges were included to assess the changes in nasal response to grass pollen allergen.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Allergic Rhinitis Due to Grass Pollens
7. Study Design
Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
40 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Control group
Arm Type
No Intervention
Arm Title
Subcutaneous Immunotherapy (SCIT)
Arm Type
Active Comparator
Arm Description
Treatment using ALK AluTard 225 "Phleum pratense"
Arm Title
Sublingual Allergen Immunotherapy Tablets (AIT)
Arm Type
Active Comparator
Arm Description
Treatment using ALK Grazax 75,000 SQ-T "Phleum pratense"
Intervention Type
Drug
Intervention Name(s)
ALK Grazax 75,000 SQ-T "Phleum pratense"
Intervention Type
Drug
Intervention Name(s)
ALK AluTard 225 "Phleum pratense"
Primary Outcome Measure Information:
Title
Changes over time in specific Antibodies
Description
IgE, IgG4
Time Frame
0, 1, 2, 3, 6, 7, 10, 12, and 15 months post treatment start
Title
Changes over time in Basophil Activation Test
Time Frame
0, 1, 3, 6, 7, 10, 12, and 15 months post treatment start
Secondary Outcome Measure Information:
Title
Changes over time in Nasal Challenge symptoms
Time Frame
0, 3, 10, and 15 months post treatment start
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
history of rhinitis with hay fever symptoms during the grass pollen season,
a skin-prick-test-verified grass pollen allergy (Phleum pratense),
eligibility for immunotherapy based on ARIA guidelines
Exclusion Criteria:
current long-term systemic steroid treatment,
previous immunotherapy,
asthma and outside-season airway hyperresponsiveness (AHR) (September 2011),
pregnancy,
negative RAST for grass, and
treatment side effect
Facility Information:
Facility Name
Bispebjerg University Hospital
City
Copenhagen NV
ZIP/Postal Code
2400
Country
Denmark
12. IPD Sharing Statement
Citations:
PubMed Identifier
24734285
Citation
Aasbjerg K, Backer V, Lund G, Holm J, Nielsen NC, Holse M, Wagtmann VR, Wurtzen PA. Immunological comparison of allergen immunotherapy tablet treatment and subcutaneous immunotherapy against grass allergy. Clin Exp Allergy. 2014 Mar;44(3):417-28. doi: 10.1111/cea.12241.
Results Reference
derived
Learn more about this trial
Immunological Comparison of AIT and SCIT Immunotherapy Against Grass Pollen
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