Does Sphingosine-1-phosphate Constrict Human Airways? In-vivo Challenge Pilot Study.
试验速览
- 阶段
- 不适用
- 入组人数
- 12
- 试验地点
- 1
- 主要终点
- Bronchoconstriction
研究概览
简要总结
This study is being undertaken in order to enhance our understanding how human airways are being constricted in healthy people and in individuals with asthma. There is an unmet need for identification of new pathways (mediators) related to enhanced constriction of the asthmatic airways that would reveal new targets for therapy. Sphingosine-1-phosphate (S1P) is a naturally occurring bioactive lipid molecule that has been suggested to play an important role in asthma. Physiologically, S1P can be detected in human blood but local tissue concentrations (for example in the lung) are very low. Upon activation many cells can secrete S1P. Increased concentrations of S1P have been detected in airways of asthmatic subjects after allergen inhalation. When studied in animal models, S1P did not cause contraction of airways in healthy animals but contracted airways in animal with pulmonary inflammation. In laboratory experiments S1P has been shown to be a potent constrictor of cells responsible for contraction of human airways. As yet, however, we lack evidence that S1P actually causes constriction of airways in real life. Establishing S1P as a molecule capable of causing airway constriction in humans and perhaps specifically in asthmatics will have important implications for our understanding of physiological and pathophysiological responses in human airways and could open new windows for therapeutic strategies in diseases like asthma.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Basic Science
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 65 Years(Adult, Older Adult)
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Cases (asthmatics) inclusion criteria
- •1. Physician diagnosed asthma, defined as a clear history of typical symptoms and clear reversibility of the PEF/FEV1 (12% or more) within the past year and/or methacholine PC20 < 8mg/ml.
排除标准
- •Pregnancy or lactation
- •Moderate / Severe asthma (FEV1/PEF < 80%of the predicted value at screening)
- •Patients with any chronic illness other than asthma and other recognised atopic diseases (eczema, rhinitis) or any other abnormality which in the opinion of the principal investigator might compromise the study findings
- •A history of recent (within the past 4 weeks) upper or lower respiratory tract infection
- •Patients receiving oral, inhaled or parenteral glucocorticoid therapy (steroid) within the last 4 weeks, long acting relievers (salmeterol, formoterol) and antileukotrienes (montelukast) within last 72 hours.
- •Inadequate contraception in women of childbearing age
- •Inability to comprehend or comply with the protocol
- •Controls inclusion criteria
- •1. Lifelong absence of asthma symptoms and lung function within the normal range.
- •Controls exclusion criteria
- •Pregnancy or lactation
- •Patients with any chronic illness or any other abnormality which in the opinion of the principal investigator might compromise the study findings
- •A history of recent (within the past 4 weeks) upper or lower respiratory tract infection
- •Oral, inhaled or parenteral glucocorticoid therapy (steroid) within the last 4 weeks, long acting relievers (salmeterol, formoterol) and antileukotrienes (montelukast) within last 72 hours
- •Inadequate contraception in women of childbearing age
- •Inability to comprehend or comply with the protocol
结局指标
主要结局
Bronchoconstriction
时间窗: 1 hour after challenge
Bronchoconstriction in response to challenge measured by spirometry (FEV1)(PC20)
次要结局
未报告次要终点
