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Evaluating the in vivo Th2 priming potential among common allergens
Exposure to allergens, both man-made and from our environment is increasingly associated with the development of significant human health issues such as allergy and asthma. Allergen induced production of the cytokine interleukin (IL-)4 by Th2 cells is central to the pathogenesis of allergic disease...
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Published in: | Journal of immunological methods 2013-08, Vol.394 (1-2), p.62-72 |
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container_title | Journal of immunological methods |
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creator | Camberis, Mali Prout, Melanie Tang, Shiau-Choot Forbes-Blom, Elizabeth Robinson, Marcus Kyle, Ryan Belkaid, Yasmine Paul, William Le Gros, Graham |
description | Exposure to allergens, both man-made and from our environment is increasingly associated with the development of significant human health issues such as allergy and asthma. Allergen induced production of the cytokine interleukin (IL-)4 by Th2 cells is central to the pathogenesis of allergic disease (Gavett et al., 1994). The development of the G4 mouse, that expresses green fluorescent protein (GFP) as a surrogate for IL-4 protein expression has made it possible to directly track the immune cells that produce IL-4. By combining a reliable intradermal immunisation technique with the transgenic G4 mouse we have been able to develop a novel & unique in vivo primary Th2 immune response model (PTh2). When allergens relevant to human disease are evaluated using the PTh2 assay a dose dependent hierarchy of allergenicity is revealed with environmental allergens (cockroach, house dust mite) the most potent and food allergens being the least. In addition, the PTh2 assay is extremely sensitive to the immunoregulatory effects of Mycobacterial extracts and immunosuppressive drugs on primary Th2 cell development. Taken together, this assay provides a standardised method for the identification of the structural and functional properties of proteins relevant to allergenicity, and is a powerful screening tool for novel lead compounds that are effective at inhibiting the primary Th2 response in allergic diseases.
•An in vivo assay that detects IL-4 producing CD4 T cells•Primary immune response without multiple immunisations or adjuvants•Highly sensitive and quantitative allowing comparisons between allergens•Independent of the influence of endotoxin•Can measure suppression by pharmacological agents |
doi_str_mv | 10.1016/j.jim.2013.05.004 |
format | article |
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Taken together, this assay provides a standardised method for the identification of the structural and functional properties of proteins relevant to allergenicity, and is a powerful screening tool for novel lead compounds that are effective at inhibiting the primary Th2 response in allergic diseases.
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subjects | Allergenicity Allergens - immunology Animals CD4 T cell CD4-Positive T-Lymphocytes - immunology eGFP-reporter Female House dust mite Humans In vivo Th2 immunoassay Interleukin-4 Lipopolysaccharides - pharmacology Male Mice Mice, Inbred C57BL Skin - immunology Th2 Cells - immunology |
title | Evaluating the in vivo Th2 priming potential among common allergens |
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