Investigating Immune Gene Signatures in Peripheral Blood from Subjects with Allergic Rhinitis Undergoing Nasal Allergen Challenge

被引:8
作者
Kim, Young Woong [1 ,2 ,3 ]
Singh, Amrit [1 ,2 ,3 ]
Shannon, Casey P. [3 ]
Thiele, Jenny [4 ,5 ]
Steacy, Lisa M. [5 ]
Ellis, Anne K. [4 ,5 ,6 ]
Neighbour, Helen [7 ,8 ]
Gliddon, Daniel R. [9 ]
Hickey, Pascal L. C. [10 ]
Larche, Mark [7 ,8 ]
Tebbutt, Scott J. [1 ,2 ,11 ]
机构
[1] Univ British Columbia, Expt Med, Vancouver, BC V5Z 1M9, Canada
[2] St Pauls Hosp, Ctr Heart Lung Innovat, Room 166,1081 Burrard St, Vancouver, BC V6Z 1Y6, Canada
[3] Prevent Organ Failure Ctr Excellence, Vancouver, BC V6Z 2K5, Canada
[4] Queens Univ, Dept Med, Kingston, ON K7L 3N6, Canada
[5] Kingston Gen Hlth Res Inst, Kingston Allergy Res, Kingston, ON K7L 2V7, Canada
[6] Queens Univ, Dept Biomed & Mol Sci, Kingston, ON K7L 3N6, Canada
[7] McMaster Univ, Dept Med, Hamilton, ON L8S 4L8, Canada
[8] McMaster Univ, Firestone Inst Resp Hlth, Hamilton, ON L8N 4A6, Canada
[9] Circassia Ltd, Oxford OX4 4GA, England
[10] Adiga Life Sci, Hamilton, ON L8P 0A1, Canada
[11] Univ British Columbia, Dept Med, Resp Div, Vancouver, BC V5Z 1M9, Canada
关键词
EOSINOPHIL RECRUITMENT; MAST-CELLS; PATHOPHYSIOLOGY; EXPRESSION; OPTIMIZATION; SYMPTOMS; EXPOSURE; HEALTH; PHASE; MODEL;
D O I
10.4049/jimmunol.1700378
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Nasal allergen challenge (NAC) is a human model of allergic rhinitis (AR) that delivers standardized allergens locally to the nasal mucosa allowing clinical symptoms and biospecimens such as peripheral blood to be collected. Although many studies have focused on local inflammatory sites, peripheral blood, an important mediator and a component of the systemic immune response, has not been well studied in the setting of AR. We sought to investigate immune gene signatures in peripheral blood collected after NAC under the setting of AR. Clinical symptoms and peripheral blood samples from AR subjects were collected during NAC. Fuzzy c-means clustering method was used to identify immune gene expression patterns in blood over time points (before NAC and 1, 2, and 6 h after NAC). We identified and validated seven clusters of differentially expressed immune genes after NAC onset. Clusters 2, 3, and 4 were associated with neutrophil and lymphocyte frequencies and neutrophil/lymphocyte ratio after the allergen challenge. The patterns of the clusters and immune cell frequencies were associated with the clinical symptoms of the AR subjects and were significantly different from healthy nonallergic subjects who had also undergone NAC. Our approach identified dynamic signatures of immune gene expression in blood as a systemic immune response associated with clinical symptoms after NAC. The immune gene signatures may allow cross-sectional investigation of the pathophysiology of AR and may also be useful as a potential objective measurement for diagnosis and treatment of AR combined with the NAC model.
引用
收藏
页码:3395 / 3405
页数:11
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