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Tyrphostin AG-490 inhibits cytokine-mediated JAK3/STAT5a/b signal transduction and cellular proliferation of antigen-activated human T cells

  1. Author:
    Kirken, R. A.
    Erwin, R. A.
    Taub, D.
    Murphy, W. J.
    Behbod, F.
    Wang, L. H.
    Pericle, F.
    Farrar, W. L.
  2. Author Address

    Kirken RA Univ Texas, Hlth Sci Ctr, Dept Integrat Biol & Pharmacol MSB Rm 4-218 Houston, TX 77030 USA Univ Texas, Hlth Sci Ctr, Dept Integrat Biol & Pharmacol Houston, TX 77030 USA Frederick Canc Res & Dev Ctr, SAIC Frederick, IRSP Frederick, MD USA NIA, Immunol Lab Baltimore, MD 21224 USA NCI, Expt Immunol Branch, NIH Bethesda, MD 20892 USA NCI, Div Basic Sci,Cytokine Mol Mechanisms Sect, Mol Immunoregulat Lab, Frederick Canc Res & Dev Ctr Frederick, MD 21701 USA
    1. Year: 1999
  1. Journal: Journal of Leukocyte Biology
    1. 65
    2. 6
    3. Pages: 891-899
  2. Type of Article: Article
  1. Abstract:

    Janus kinase 3 (JAK3) is a cytoplasmic tyrosine kinase required for T cell development and activated by cytokines that utilize the interleukin-2 (IL-2) receptor common gamma chain (gamma(c)). Genetic inactivation of JAK3 is manifested as severe combined immunodeficiency disease (SCID) in humans and mice. These findings have suggested that JAK3 represents a pharmacological target to control certain lymphoid-derived diseases. Here we provide novel evidence that AG-490 potently inhibits the autokinase activity of JAK3 and tyrosine phosphorylation and DNA binding of signal transducer and activator of transcription 5a and 5b (STAT5a/b), Similar inhibitory effects were observed with other cytokines that use gamma(c). AG-490 also inhibited IL-2-mediated proliferative growth in human T cells with an IC50 = 25 mu M that was partially recoverable. Moreover, we demonstrate that this inhibitor prevented tetanus toroid antigen-specific T cell proliferation and expansion but failed to block activation of Zap70 or p56Lck after anti-CD3 stimulation of human T cells. Taken together, these findings suggest that AG-490 inhibits the JAK3-mediated Type II signaling pathway but not the T cell receptor-derived Type I pathway and possesses therapeutic potential for T cell-derived pathologies such as graft-versus-host disease, allergy, and autoimmune disorders. [References: 35]

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