Abstract

Interleukin-12 (IL-12) is a heterodimeric pro-inflammatory cytokine that induces the production of interferon- (IFN-), favours the differentiation of T helper 1 (T_H1) cells and forms a link between innate resistance and adaptive immunity. Dendritic cells (DCs) and phagocytes produce IL-12 in response to pathogens during infection. Production of IL-12 is dependent on differential mechanisms of regulation of expression of the genes encoding IL-12, patterns of Toll-like receptor (TLR) expression and cross-regulation between the different DC subsets, involving cytokines such as IL-10 and type I IFN. Recent data, however, argue against an absolute requirement for IL-12 for T_H1 responses. Our understanding of the relative roles of IL-12 and other factors in T_H1-type maturation of both CD4⁺ and CD8⁺ T cells is discussed here, including the participation in this process of IL-23 and IL-27, two recently discovered members of the new family of heterodimeric cytokines.

Author affiliations

1. Laboratory for Immunological Research, Schering-Plough Research Institute, 27 Chemin des Peupliers, B.P. 11, 69571 Dardilly, France.
   Email: Giorgio.Trinchieri@spcorp.com