Allergen-induced production of IL-31 by canine Th2 cells and identification of immune, skin, and neuronal target cells
Autor: | Andrea J Gonzales, Gregory J. Fici, Michelle Aleo, James E. Messamore, Erin E. McCandless, Catherine Rugg |
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Rok vydání: | 2013 |
Předmět: |
Keratinocytes
medicine.medical_treatment T cell Immunology Inflammation IL-31 Enzyme-Linked Immunosorbent Assay Biology Real-Time Polymerase Chain Reaction Peripheral blood mononuclear cell Canine Dermatitis Atopic Th2 Interferon-gamma Immune system Dogs Th2 Cells Antigen medicine Animals Antigens Dermatophagoides Dog Diseases Dorsal root ganglia General Veterinary ELISPOT Macrophages Interleukins veterinary(all) Cytokine medicine.anatomical_structure Cell culture Leukocytes Mononuclear RNA Interleukin-4 medicine.symptom |
Zdroj: | Veterinary immunology and immunopathology. 157(1-2) |
ISSN: | 1873-2534 |
Popis: | The canine cytokine IL-31 induces pruritus in dogs and can be detected in dogs with atopic dermatitis; however very little is understood around its interactions with specific canine cells. We hypothesize that IL-31 is involved in the progression of allergic skin disease by coordinating the interaction between the immune system with skin and neuronal systems. The goal of the following work was to identify cells that produce IL-31 as well as cells that may respond to this cytokine. Peripheral blood mononuclear cells (PBMCs) were collected from naïve and house dust mite (HDM) allergen-sensitized beagle dogs and used for ex vivo characterization of cytokine production assessed using ELISpot and quantitative immunoassay. Sensitization to HDM allergen induced a T-helper type 2 (Th2) cell phenotype characterized by an increase in the production of IL-4 protein. Interestingly, repeated allergen challenge over time also resulted in an increase in IFN-γ. Further evaluation showed that co-stimulation of Th2 polarized cells with antigen and the bacterial component Staphylococcus enterotoxin B (SEB) produced higher levels of IL-31 compared to either stimulant alone. Production of IL-31 when PBMCs were stimulated by T cell mitogens suggests T cells as a source of IL-31. Quantitative real-time PCR was utilized to determine expression of the IL-31 receptor alpha chain in canine cell lines and tissue. Canine monocytic cells, keratinocytes, and dorsal root ganglia were shown to express the IL-31 receptor alpha chain mRNA. In a multifaceted disease such as canine atopic dermatitis, the combination of Th2 polarization and microbial presence may lead to IL-31 mediated effects driving inflammation and pruritus by immune cells, keratinocytes, and direct neuronal stimulation. |
Databáze: | OpenAIRE |
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