Mechanisms of Interplay Between Allergy and Viruses in Asthma

NCT01773590 | Completed DMC

• 1 other identifier: 12/LO/1278
• Study Type: interventional
• Target: 43
• Locations: 1 country
• Sites: 1

Brief Summary

The aim of this study is to investigate the mechanisms of interplay between allergy (IgE and Th2 mediated inflammation) and virus infection in the development of asthma, as well as the risk and severity of acute exacerbations of asthma. Understanding these mechanisms should identify new approaches for novel therapies for the prevention of asthma development and for prevention/treatment of asthma exacerbations. Such treatment has potential to have a major impact on patient quality of life and to result in enormous reductions in health care costs. A human model will be used to identify dysregulated genes/proteins and determine relationships with disease outcomes. This study will compare lower airway responses between asthmatic and healthy control subjects undergoing rhinovirus (RV) experimental infection (subjects will be infected with rhinovirus as part of the study). This will have the dual advantage of investigating mechanisms in the most natural model possible, as well as developing a better model for testing novel therapeutic approaches. The investigators will analyse the samples from both subject groups, to determine their relevance to the human disease. Any genes/proteins shown to be dysregulated and related to disease outcomes in the human model will be very strong candidates for immediate translation into human intervention studies. Up to 12 asthmatic and/or healthy subjects will be recruited for a preliminary pilot study. These subjects will be ineligible to enter the main study due to the presence of neutralizing antibody to RV16 (\~50% of subjects otherwise suitable for the study). These subjects will meet all other inclusion/exclusion criteria for the main study. The 12 participants will undergo tests including a single bronchoscopy, nasal sampling and blood tests allowing for optimisation of all sample processing techniques. They will not be infected with RV-16. In the main study the investigators will aim to study up to 15 healthy volunteers and 15 volunteers with moderate asthma (all on inhaled steroid treatment). Subjects will undergo a single baseline bronchoscopy 2 weeks prior to inoculation with the RV16 virus. Following infection with the virus participants will be required to attend for regular sample collection including 2 further bronchoscopies post-infection. Patients will be followed until convalescence 6 weeks post infection.

Conditions

Rhinovirus Infection in Asthma

Outcome Measures

Primary Outcomes (1)

• Host response to RV challenge

  The host response to RV challenge will be assessed daily for 8 days using methods including symptom diaries, lung function, detection of mediators in nasal and bronchial lining fluid, characterisation of different cell types in bronchoalveolar lavage as determined by flow cytometry. This will be compared with findings at baseline, day 11, 15 and up to 42 days post challenge.

  Prior to and 0-42 days post challenge

Study Arms (2)

Asthmatics

OTHER

Rhinovirus Infection

Other: Rhinovirus Infection

Healthy Volunteers

OTHER

Rhinovirus Infection

Other: Rhinovirus Infection

Interventions

Rhinovirus Infection OTHER

Asthmatics; Healthy Volunteers

Eligibility Criteria

• Age: 18 Years - 55 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)

You may qualify if:

• Age 18-55 years
• Doctor diagnosis of Asthma
• Histamine PC20 \< 8 µg/ml (or \<12 µg/ml and bronchodilator response ≥ 12%) and worsening asthma symptoms with infection since last change in asthma therapy
• Atopic on skin testing
• Treatment comprising ICS or combination inhaler (LABA+ICS)
• \*subjects on inhaled corticosteroids must be on a daily dose of 400mcg fluticasone or equivalent.
• An Asthma Control Questionnaire (ACQ) score of \> 0.75.
• Age 18-55 years
• No history or clinical diagnosis of asthma
• No history of allergic rhinitis or eczema
• Negative responses on skin prick testing
• PC20 \> 8 µg/ml and bronchodilator response \<12%
• Absence of current or previous history of significant respiratory disease
• Absence of significant systemic disease

You may not qualify if:

• Smoking history over past 6 months
• Negative skin prick tests
• Current symptoms of allergic rhinitis
• Current or previous history of significant respiratory disease (other than asthma)
• Any clinically relevant abnormality on screening or detected significant systemic disease
• Pregnant or breastfeeding women
• Contact with infants or elderly at home or at work
• Asthma exacerbation or viral illness within the previous 6 weeks
• Treatment with oral steroids now or in the previous 3 months
• Current use of nasal spray, anti-histamine, anti-leukotrienes
• Antibodies to rhinovirus 16 in a titre \>1:2
• Any clinically relevant abnormality on screening or detected significant systemic disease
• A current or previous diagnosis of asthma
• Any positive skin prick test
• Current symptoms of allergic rhinitis

Sponsors & Collaborators

• Imperial College London: lead

Study Sites (1)

National Heart and Lung Institute

London, London, United Kingdom

Location

Study Officials

• Sebastian Johnston

  National Heart and Lung Institute

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NON RANDOMIZED
• Masking: NONE
• Purpose: BASIC SCIENCE
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: November 30, 2012
• First Posted: January 23, 2013
• Study Start: February 1, 2013
• Primary Completion: August 1, 2015
• Study Completion: January 1, 2016
• Last Updated: February 17, 2016

Record last verified: 2016-01

Locations

GB (1)