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April 1, 2001Annual Review of Immunology1,329 citations

Interleukin-18 Regulates Both Th1 and Th2 Responses

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KNKenji NakanishiTYTomohiro YoshimotoHTHiroko Tsutsui

Key Points

  • This research examines the regulatory roles of interleukin-18 in Th1 and Th2 immune responses and its implications in inflammatory disorders.
  • Analyzed interleukin-18 production from various immune and non-immune cells.
  • Studied the effects of interleukin-18 on Th1 and Th2 cytokine production in vitro.
  • Investigated the expression of IL-18 mRNA in different cell types.
  • IL-18 significantly enhances IL-12-driven Th1 responses, promoting IFN-gamma production.
  • IL-18 also independently stimulates Th2 cytokine production associated with allergic inflammation.
  • Overproduction of IL-18 is linked to severe inflammatory disorders.

Abstract

Although interleukin-18 is structurally homologous to IL-1 and its receptor belongs to the IL-1R/Toll-like receptor (TLR) superfamily, its function is quite different from that of IL-1. IL-18 is produced not only by types of immune cells but also by non-immune cells. In collaboration with IL-12, IL-18 stimulates Th1-mediated immune responses, which play a critical role in the host defense against infection with intracellular microbes through the induction of IFN-gamma. However, the overproduction of IL-12 and IL-18 induces severe inflammatory disorders, suggesting that IL-18 is a potent proinflammatory cytokine that has pathophysiological roles in several inflammatory conditions. IL-18 mRNA is expressed in a wide range of cells including Kupffer cells, macrophages, T cells, B cells, dendritic cells, osteoblasts, keratinocytes, astrocytes, and microglia. Thus, the pathophysiological role of IL-18 has been extensively tested in the organs that contain these cells. Somewhat surprisingly, IL-18 alone can stimulate Th2 cytokine production as well as allergic inflammation. Therefore, the functions of IL-18 in vivo are very heterogeneous and complicated. In principle, IL-18 enhances the IL-12-driven Th1 immune responses, but it can also stimulate Th2 immune responses in the absence of IL-12.

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Cite This Study

Nakanishi et al. (2001) studied this question.

synapsesocial.com/papers/69fbf9e863c66095a8df7292https://doi.org/10.1146/annurev.immunol.19.1.423
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