A novel immunoregulatory function for IL-23: Inhibition of IL-12-dependent IFN-[gamma] production

• Published in: European journal of immunology 2010-08, Vol.40 (8), p.2236
• Main Authors: Sieve, Amy N, Meeks, Karen D, Lee, Suheung, Berg, Rance E
• Format: Article
• Language: English
• Subjects: Lymphocytes; Rodents
• ISSN: 0014-2980; 1521-4141
• DOI: 10.1002/eji.200939759

Most studies investigating the function of IL-23 have concluded that it promotes IL-17-secreting T cells. Although some reports have also characterized IL-23 as having redundant pro-inflammatory effects with IL-12, we have instead found that IL-23 antagonizes IL-12-induced secretion of IFN-[gamma]. When splenocytes or purified populations of T cells were cultured with IL-23, IFN-[gamma] secretion in response to IL-12 was dramatically reduced. The impact of IL-23 was most prominent in CD8+ T cells, but was also observed in NK and CD4+ T cells. Mechanistically, the IL-23 receptor was not required for this phenomenon, and IL-23 inhibited signaling through the IL-12 receptor by reducing IL-12-induced signal transducer and activator of transcription 4 (STAT4) phosphorylation. IL-23 was also able to reduce IFN-[gamma] secretion by antagonizing endogenously produced IL-12 from Listeria monocytogenes (LM)-infected macrophages. In vivo, LM infection induced higher serum IFN-[gamma] levels and a greater percentage of IFN-[gamma]+CD8+ T cells in IL-23p19-deficient mice as compared with WT mice. This increase in IFN-[gamma] production coincided with increased LM clearance at days 2 and 3 post-infection. Our data suggest that IL-23 may be a key factor in determining the responsiveness of lymphocytes to IL-12 and their subsequent secretion of IFN-[gamma].