Free Content Antigen-induced IL-17 response in the peripheral blood mononuclear cells (PBMC) of healthy controls

Authors: Lenarczyk, A.1; Helsloot, J.1; Farmer, K.1; Peters, L.1; Sturgess, A.1; Kirkham, B.1

Source: Clinical & Experimental Immunology, Volume 122, Number 1, October 2000 , pp. 41-48(8)

Publisher: Blackwell Publishing

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Abstract:

IL-17 is a T cell cytokine with a complex and important role in the immune system. It has been detected in rheumatoid arthritis (RA) synovial membrane and found to stimulate the production of the proinflammatory cytokines IL-6, IL-8, tumour necrosis factor-alpha (TNF-α) and granulocyte-macrophage colony-stimulating factor (GM-CSF) in vitro. To date, there are few data available on the agents that stimulate IL-17 production. We therefore investigated the in vitro IL-17 response to a variety of mitogens and antigens, and compared the IL-17 response to interferon-gamma (IFN-γ), IL-4, IL-10 and TNF-α. In this study we used a type-0 antigen, tetanus toxoid (TT), a type-1 antigen, PPD from Mycobacterium tuberculosis, a potential type-2 rye grass (RG) antigen (Lol I) and an autoantigen SS.B (La), to stimulate PBMC from healthy controls. Cytokine mRNA was measured using semiquantitative reverse transcriptase-polymerase chain reaction and cytokine protein measured using specific ELISA techniques, while the frequency of IL-17-producing T cells was determined by flow cytometry. The mitogens concanavalin A, phytohaemagglutinin and phorbol myristate acetate/ionomycin induced a significant increase in IL-17, with the highest levels being produced by anti-CD3/anti-CD28 stimulation. The antigens TT and PPD significantly increased IL-17 mRNA expression over time, but failed to have such an effect at the protein level. IL-17 protein was also detectable in both antigen-specific (TT, SS.B) and non-specific T cell clones, but at levels lower than IFN-γ. IL-17 production did not correlate with either the type-1 cytokine IFN-γ or TNF-α or the type-2 cytokine IL-4 or IL-10 at either the mRNA or protein level.

Keywords: IL-17; antigens; cytokines

Document Type: Research article

DOI: 10.1046/j.1365-2249.2000.01328.x

Affiliations: 1: Department of Rheumatology, St George Hospital, Kogarah, Australia

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