Mechanisms of Allergen Immunotherapy

NCT ID: NCT01523158

Last Updated: 2012-09-25

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: NA
• Total Enrollment: 2 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2012-04-30
• Study Completion Date: 2015-09-30

Brief Summary

Hay fever (seasonal allergic rhinitis) results from allergy to grass and tree pollen. The majority of affected individuals manage well with medication from the Pharmacy or from their general practitioner (GP), but for some severely affected people it severely impacts on quality of life. Less than 40% of those affected in UK general practice feel that these medications achieve good symptomatic control.

Specific immunotherapy or desensitisation is the practice of administering small amounts of allergen to allergic patients in increasing doses. This treatment is highly effective in these patients and furthermore is truly disease-modifying, with benefits persisting long-term, even when the treatment has been completed. Desensitisation is a routine treatment in the UK, Europe and North America. The exact immune mechanisms that underlie this symptomatic improvement are not entirely clear. Dr Tarzi, Professor Frew and Professor Kern have recently developed new methods for the investigation of immune responses to allergens. These methods require relatively small blood samples and may provide useful information about how immunotherapy exerts its effects. In addition to improving the investigators basic understanding of this treatment, such knowledge may drive improvements in the treatment and could be useful for monitoring patients for response. The investigators study proposes to investigate changes in the immune responses to pollen allergens during immunotherapy. Blood will be taken just prior to the first immunotherapy injection and again just prior to the final injection. In this way the investigators will be able to compare the immune responses to pollen allergen before and after treatment.

Conditions

Allergic Rhinitis

Keywords

Allergic Rhinitis; Immunotherapy

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: NONE

Study Groups

Immunotherapy

Open label study of changes to cellular responses following immunotherapy

Group Type: OTHER

Allergovit grass or birch

Intervention Type: BIOLOGICAL

subcutaneous injection of immunotherapy once weekly for 7 weeks prior to birch pollen season.

Interventions

Allergovit grass or birch

subcutaneous injection of immunotherapy once weekly for 7 weeks prior to birch pollen season.

Intervention Type: BIOLOGICAL

Eligibility Criteria

Inclusion Criteria

• Male or female
• Age 18 with no upper age limit
• History of seasonal rhino-conjunctivitis in the appropriate season, not controlled by optimised standard medical therapy
• Positive skin prick test to grass pollen or tree pollen

Exclusion Criteria

• Inadequately controlled or moderate to severe asthma (GINA III/IV), i.e. the FEV1 is below 70 % of the target value despite adequate pharmacotherapy
• Irreversible changes in the reaction organ (emphysema, bronchiectasis, etc.)
• Clinically significant cardiovascular insufficiency (in cardiovascular diseases, there is an elevated risk of adverse reactions to adrenaline)
• Local or systemic use of beta blockers
• Diseases of the immune system (autoimmune diseases, immune complex-induced immunopathies, immunodeficiencies etc.)
• Malignant disease within the past five years (Patients with previous malignant disease that is considered cured may be included subject to the consent of their oncologist)
• Inability to attend regularly for injections and follow-up visits
• Severe atopic dermatitis
• Pregnant or not using adequate contraception (post-menopausal, surgically sterilised, long-term abstinent, or barrier methods plus spermicide)
• Breast-feeding
• Evidence of current drug or alcohol misuse
• Hypersensitivity to any of the SIT (immunotherapy product) excipients
• Active tuberculosis
• Severe mental disorders
• Multiple sclerosis

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Royal Sussex County Hospital

OTHER

Sponsor Role: lead

Responsible Party

Nicola Gray

Clinical Research Fellow

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

Royal Sussex County Hospital

Brighton, , United Kingdom

Countries

United Kingdom

Other Identifiers

12/014/TAR

Identifier Type: -

Identifier Source: org_study_id