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DOI: 10.1055/s-0039-3399658
Immunosuppressive activity of Artemisia argyi
Publication History
Publication Date:
20 December 2019 (online)
There is a need for novel immunosuppressive drugs, given that currently used small molecule drugs and biologics exhibit side effects including increased susceptibility to infections, paradoxical inflammation or autoimmune diseases [1]. Aiming at the discovery of natural products with potentially new mechanisms of action we screened a library of 435 extracts prepared from plants used in Traditional Chinese Medicine. Immunosuppressive activity of extracts was assessed in a proliferation-based assay utilizing physiologically relevant anti-CD3 and anti-CD28 stimulated primary human T lymphocytes [2]. An ethyl acetate extract of Artemisia argyi H. Lév. & Vaniot (Asteraceae) was found to be highly active with an IC50 of 16.2 µg/mL. Apoptosis and necrosis induction analysis of T lymphocytes showed that the inhibitory effect on T cell proliferation was not due to toxic effects of the extract.
Treatment with 3 – 30 µg/mL A. argyi extract significantly lowered the expression of activation markers and suppressed the cytokine secretion of activated T lymphocytes in a dose-dependent manner. The effect of A. argyi extract on transcription factors AP-1 (activator protein 1), NF-κB (nuclear factor kappa-light-chain-enhancer of activated B cells) and NFAT (nuclear factor of activated T-cells) was investigated. Results point to a specific suppression of transcription factors leading to a diminished expression of IL-2 and, as a consequence, to inhibition of T cell proliferation. Compounds responsible for the effects are currently being tracked by HPLC-based activity profiling [3], mode-of-action studies are ongoing.
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References
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- 3 Potterat O, Hamburger M. Combined use of extract libraries and HPLC-based activity profiling for lead discovery: potential, challenges, and practical considerations. Planta Med 2014; 80: 1171-1181