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Novel p19 protein engages IL-12p40 to form a cytokine, IL-23, with biological activities similar as well as distinct from IL-12

  • Birgit Oppmann
  • , Robin Lesley
  • , Bianca Blom
  • , Jackie C. Timans
  • , Yuming Xu
  • , Brisdell Hunte
  • , Felix Vega
  • , Nancy Yu
  • , Jing Wang
  • , Komal Singh
  • , Francesca Zonin
  • , Elena Vaisberg
  • , Tatyana Churakova
  • , Man ru Liu
  • , Daniel Gorman
  • , Janet Wagner
  • , Sandra Zurawski
  • , Yong Jun Liu
  • , John S. Abrams
  • , Kevin W. Moore
  • Donna Rennick, Rene De Waal-Malefyt, Charles Hannum, J. Fernando Bazan, Robert A. Kastelein
  • Merck

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

A novel sequence discovered in a computational screen appears distantly related to the p35 subunit of IL-12. This factor, which we term p19, shows no biological activity by itself; instead, it combines with the p40 subunit of IL-12 to form a novel, biologically active, composite cytokine, which we term IL-23. Activated dendritic cells secrete detectable levels of this complex. IL-23 binds to IL-12Rβ1 but fails to engage IL-12Rβ2; nonetheless, IL-23 activates Stat4 in PHA blast T cells. IL-23 induces strong proliferation of mouse memory (CD4+CD45Rb(low)) T cells, a unique activity of IL-23 as IL-12 has no effect on this cell population. Similar to IL-12, human IL-23 stimulates IFN-γ production and proliferation in PHA blast T cells, as well as in CD45RO (memory) T cells.

Original languageEnglish
Pages (from-to)715-725
Number of pages11
JournalImmunity
Volume13
Issue number5
DOIs
Publication statusPublished - Nov 2000

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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