IL-33 Production by Nasal Epithelial Cells

Overview

Información sobre este estudio

This research study is being done for people who have asthma and chronic rhinosinusitis, hay fever, or you do not have any sinus disease, asthma or hay fever (control). The aim of the study is to investigate the functions of nasal epithelial cells.

Elegibilidad para la participación

Los requisitos de elegibilidad de los participantes incluyen la edad, el sexo, el tipo y el estadio de la enfermedad, y los problemas de salud o tratamientos previos. Las pautas difieren de un estudio a otro e identifican quiénes pueden o no pueden participar. No hay garantía de que cada persona elegible que desee participar en un ensayo se inscribirá. Comunícate con el equipo del estudio para analizar la elegibilidad del estudio y la posible participación.

The inclusion criteria are as follows: 

1) Asthma and CRS:

  • Physician-diagnosed asthma

  • CRS symptoms with lasting longer than 12 weeks

  • A sinus CT scan within the past 24 months with a Lund-Mackay score > 5 (88).

2) Seasonal allergic rhinitis without asthma and CRS:

The clinical diagnosis of allergic rhinitis is established by history, where patients describe the typical seasonal signs of nose itching, sneezing and clear rhinorrhea, and is confirmed with a positive skin test and/or elevated specific serum IgE level for short ragweed antigen. 

Patients with allergic rhinitis will have no history or symptoms of asthma or of CRS, normal lung function, and negative methacholine responsiveness (PC 20 Methacholine >16 mg/ml).

3) Normal: 

The normal controls are healthy individuals with no history of allergy or CRS, normal spirometry, negative methacholine responsiveness (PC 20 Methacholine >16 mg/ml) and negative skin prick test results or negative IgE serum tests to 10 common aeroallergens.

Exclusion criteria for subjects in any group are as follows:

1) received systemic glucocorticoids or high-dose (>1,000 µg budesonide or equivalent/day) inhaled or intranasal glucocorticoids during the past 6 weeks,

2) previous or current smokers (exceeding a 10 pack year history), or

3) a lower or upper airway infection (e.g. “cold”) in the last 4 weeks.  We will also exclude volunteers who have been diagnosed with an immunodeficiency disease or cystic fibrosis. 

 

Sedes participantes de Mayo Clinic

Los estatus de los estudios cambian con frecuencia. Comunícate con el equipo del estudio para obtener la información más actualizada acerca de la posibilidad de participar.

Sede de Mayo Clinic Estatus

Rochester, Minn.

Investigador principal de Mayo Clinic

Hirohito Kita, M.D.

Cerrado para la inscripción

More information

Publicaciones

Publications are currently not available
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CLS-20318064

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