| Literature DB >> 11390444 |
T Hoshino1, Y Kawase, M Okamoto, K Yokota, K Yoshino, K Yamamura , J Miyazaki , H A Young, K Oizumi.
Abstract
IL-18 has been shown to be a strong cofactor for Th1 T cell development. However, we previously demonstrated that when IL-18 was combined with IL-2, there was a synergistic induction of a Th2 cytokine, IL-13, in both T and NK cells. More recently, we and other groups have reported that IL-18 can potentially induce IgE, IgG1, and Th2 cytokine production in murine experimental models. Here, we report on the generation of IL-18-transgenic (Tg) mice in which mature mouse IL-18 cDNA was expressed. CD8+CD44high T cells and macrophages were increased, but B cells were decreased in these mice while serum IgE, IgG1, IL-4, and IFN-gamma levels were significantly increased. Splenic T cells in IL-18 Tg mice produced higher levels of IFN-gamma, IL-4, IL-5, and IL-13 than control wild-type mice. Thus, aberrant expression of IL-18 in vivo results in the increased production of both Th1 and Th2 cytokines.Entities:
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Year: 2001 PMID: 11390444 DOI: 10.4049/jimmunol.166.12.7014
Source DB: PubMed Journal: J Immunol ISSN: 0022-1767 Impact factor: 5.422