Potential Involvement of Type I Interferon Signaling in Immunotherapy in Seasonal Allergic Rhinitis

Author:

Mattson Lina1,Lentini Antonio1,Gawel Danuta R.1,Badam Tejaswi V. S.12,Benson Mikael1,Ledin Torbjorn34,Nestor Colm E.1,Gustafsson Mika12,Serra-Musach Jordi1,Bjorkander Janne5,Xiang Zou6,Zhang Huan1ORCID

Affiliation:

1. The Centre for Personalized Medicine, Department of Clinical and Experimental Medicine, Division of Pediatrics, Linkoping University, Linkoping, Sweden

2. Bioinformatics, Department of Physics, Chemistry and Biology, Linkoping University, SE-581 83 Linkoping, Sweden

3. Division of Neuro and Inflammation Science, Department of Clinical and Experimental Medicine, Linkoping University, Linkoping, Sweden

4. Department of Otorhinolaryngology in Linkoping, Anaesthetics, Operations and Specialty Surgery Center, Region Ostergotland, Sweden

5. Futurum-Academy for Health and Care, County Council of Jonkoping, Jonkoping, Sweden

6. Department of Health Technology and Informatics, Faculty of Health and Social Sciences, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong

Abstract

Specific immunotherapy (SIT) reverses the symptoms of seasonal allergic rhinitis (SAR) in most patients. Recent studies report type I interferons shifting the balance between type I T helper cell (Th1) and type II T helper cells (Th2) towards Th2 dominance by inhibiting the differentiation of naive T cells into Th1 cells. As SIT is thought to cause a shift towards Th1 dominance, we hypothesized that SIT would alter interferon type I signaling. To test this, allergen and diluent challenged CD4+ T cells from healthy controls and patients from different time points were analyzed. The initial experiments focused on signature genes of the pathway and found complex changes following immunotherapy, which were consistent with our hypothesis. As interferon signaling involves multiple genes, expression profiling studies were performed, showing altered expression of the pathway. These findings require validation in a larger group of patients in further studies.

Funder

Swedish Research Council

Publisher

Hindawi Limited

Subject

Immunology,General Medicine,Immunology and Allergy

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