The Role of Th9 Cells and Eosinophils Activity in Allergic Airway Diseases

NCT02214303 | Unknown DMC

• 1 other identifier: SAIRA-1017/2012
• Study Type: observational
• Target: 100
• Locations: 1 country
• Sites: 1

Brief Summary

The prevalence of allergic diseases, especially airway allergic diseases, has increased dramatically over the last twenty years all over the world including Lithuania. Allergic diseases are associated with significantly reduced quality of life and can sometimes cause death. Allergic diseases have turned into an important economic and social burden and nowadays take a more and more important place in the health system. Despite all intensive investigations, the pathogenesis of allergic airway diseases still remains unclear. As allergic diseases have a systemic pattern and multicomponent pathogenesis, it is important to investigate not individual cells, but examine various inflammatory cells instead, including their biological products and possible cellular interactions along the course of allergic diseases. This research focuses on the cells that are claimed to be important in the pathogenesis of allergic airway diseases, i.e. a newly found effector T helper cell subset (Th9 cells), which still lacks deeper investigation, and the main inflammatory cell, eosinophil. This study aims at determining the importance the way the Th9 lymphocytes perform, the eosinophil's activity, as well as molecular factors affecting these cells has in the process of prognostication of allergic airway diseases, namely allergic rhinitis and allergic asthma. An allergen challenge test will be performed in order to define the meaning of pathogenetic changes. The results of this research may reveal useful information in the course of allergic diseases and may be valuable when creating strategic principles of prophylaxis. The findings could be used for prevention and early diagnostics of allergic diseases and it could also open doors to discovering new and effective treatment.

Conditions

Allergic Asthma; Allergic Rhinitis

Keywords

Allergic asthma; Allergic rhinitis; Healthy subjects

Outcome Measures

Primary Outcomes (1)

• Th9 cells and eosinophil apoptosis

  Blood and sputum eosinophils also peripheral blood th9 cells will be investigated.

  24 hours after bronchial allergen challenge

Study Arms (3)

Allergic asthma

Allergic asthma (sensibilisation to D. pteronyssinus, 5 grass mixture allergens or birch pollen allergens)

Allergic rhinitis

allergic rhinitis patients (sensibilisation to D. pteronyssinus, 5 grass mixture allergens or birch pollen allergens)

Control group

Healthy subjects

Eligibility Criteria

• Age: 18 Years - 50 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64)
• Sampling Method: Non-Probability Sample

Study Population

Allergic asthma

You may qualify if:

• Men and women between the ages of 18-50 years;
• Allergic asthma (skin prick test positive for D. pteronyssinus, 5 grass mixture or birch pollen);
• Symptoms more than one year;
• Positive Bronchial challenge with methacholine or documented completely reversible bronchial obstruction;
• Stable lung function (FEV1≥70 perc.);
• Allergic rhinitis diagnosed according ARIA criteria.
• Postmenopausal women. Premenopausal women if pregnancy test is negative
• Healthy (subjects who are not sick with acute or chronic inflammatory, infectious, oncologic or immune diseases) - control group
• Participants who gave his/her informed written consent.

You may not qualify if:

• Asthma and rhinitis exacerbation;
• Clinically significant permanent allergy symptoms (ex. cat or dog dander induced allergy);
• Active airway infection 1 month prior the study;
• Used medicaments:
• Inhaled glucocorticoids intake 1 month prior the study;
• Antihistamines intake 7 days prior the study;
• Short acting β2 agonists 12 hours prior the study;
• Long acting β2 agonists 2 days prior the study;
• Leukotriene receptor antagonists prior 14 days;
• If the histamine mean wheal diameter is \<= 3 mm or control mean wheal diameter is \>= 3 mm;
• Psychiatric disorders;
• Alcohol or narcotic abuse;
• Pregnancy.
• Breast-feeding.

Sponsors & Collaborators

• Lithuanian University of Health Sciences: lead

Study Sites (1)

Lithuanian University of Health Sciences

Kaunas, 50009, Lithuania

RECRUITING

Related Publications (1)

• Hoppenot D, Malakauskas K, Lavinskiene S, Sakalauskas R. p-STAT6, PU.1, and NF-kappaB are involved in allergen-induced late-phase airway inflammation in asthma patients. BMC Pulm Med. 2015 Oct 14;15:122. doi: 10.1186/s12890-015-0119-7.

  PMID: 26466682 DERIVED

Biospecimen

Retention: SAMPLES WITHOUT DNA

Induced sputum and peripheral blood samples

MeSH Terms

Conditions

Rhinitis, Allergic

Condition Hierarchy (Ancestors)

Rhinitis; Nose Diseases; Respiratory Tract Diseases; Respiratory Hypersensitivity; Otorhinolaryngologic Diseases; Hypersensitivity, Immediate; Hypersensitivity; Immune System Diseases

Study Officials

• Raimundas Sakalauskas, Prof., dr.

  Lithuanian University of Health Sciences, Pulmonology and Immunology department

  STUDY CHAIR

Central Study Contacts

Raimundas Sakalauskas, prof., dr.

CONTACT

376953; raimundas.sakalauskas@kaunoklinikos.lt

Deimante Hoppenot, MD

CONTACT

67439677; deimante@gmail.com

Study Design

• Study Type: observational
• Time Perspective: PROSPECTIVE
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: prof., dr.

Study Record Dates

• First Submitted: August 6, 2014
• First Posted: August 12, 2014
• Study Start: April 1, 2013
• Primary Completion: September 1, 2015
• Study Completion: December 1, 2015
• Last Updated: August 12, 2014

Record last verified: 2014-08

Locations

LI (1)