• Medientyp: E-Artikel
  • Titel: Generation of CD8 T Cell Memory Is Regulated by IL-12
  • Beteiligte: Pearce, Erika L.; Shen, Hao
  • Erschienen: The American Association of Immunologists, 2007
  • Erschienen in: The Journal of Immunology, 179 (2007) 4, Seite 2074-2081
  • Sprache: Englisch
  • DOI: 10.4049/jimmunol.179.4.2074
  • ISSN: 0022-1767; 1550-6606
  • Entstehung:
  • Anmerkungen:
  • Beschreibung: <jats:title>Abstract</jats:title> <jats:p>Various signals during infection influence CD8 T cell memory generation, but these factors have yet to be fully defined. IL-12 is a proinflammatory cytokine that has been shown to enhance IFN-γ-producing T cell responses and has been widely tested as a vaccine adjuvant. In this study, we show that IL-12-deficient mice generate a weaker primary CD8 T cell response and are more susceptible to Listeria monocytogenes infection, but have substantially more memory CD8 T cells and greater protective immunity against reinfection. Kinetic analyses show that in the absence of IL-12 there is a reduced contraction of Ag-specific CD8 T cells and a gradual increase in memory CD8 T cells as a result of increased homeostatic renewal. By signaling directly through its receptor on CD8 T cells, IL-12 influences their differentiation to favor the generation of fully activated effectors, but hinders the formation of CD8 T cell memory precursors and differentiation of long-term CD8 T cell memory. These results have implications for understanding memory T cell development and enhancing vaccine efficacy, and offer new insight into the role of IL-12 in coordinating the innate and adaptive immune response.</jats:p>
  • Zugangsstatus: Freier Zugang