Both MF59 and AS03 are squalene-based oil-in-water emulsion adjuvants and AS04 is a combination of two adjuvants, alum and monophosphoryl lipid A [7]. Given the lack of licensed adjuvants, the search for new vaccine adjuvants is a high priority for vaccinologists. 3′, 5′-Cyclic diguanylic acid (Fig. 1 where X = Y = O) is an intracellular signaling molecule first identified in Gluconacetobacter xylinus (formerly Acetobacter xylinum) where it regulates cellulose production by modulating cellulose synthase activity [8]. Research has suggested that c-di-GMP-mediated

signaling is widespread in bacterial species from Escherichia coli to Bacillus subtilis to Caulobacter crescentus Palbociclib concentration [9], [10] and [11]. However, it has not been found in higher eukaryotes [9], leading many to believe that c-di-GMP signaling is an exclusively bacterial

characteristic. Its seemingly ubiquitous presence in bacteria would seem to suggest that c-di-GMP plays a role in one or more critical bacterial functions and in fact, an increasing body of research has revealed the importance of c-di-GMP as a bacterial second messenger (cf. [12], [13] and [14]) in the regulation of many physiological processes important for bacterial survival (such as adhesion, cell-to-cell communication, exopolysaccharide synthesis, buy Cabozantinib and motility [15], [16], [17] and [18]). The recent finding that c-di-GMP can act as a danger signal on eukaryotic cells [19] has prompted the study of the immunostimulatory and immunomodulatory properties of c-di-GMP Thiamine-diphosphate kinase in an effort to determine whether c-di-GMP might be further developed as

a potential vaccine adjuvant. This review focuses on the recent studies of the immunostimulatory properties of c-di-GMP and the progress that has been made in the preclinical development of c-di-GMP as a potential vaccine adjuvant for systemic and mucosal vaccination ( Table 1). Several studies have now convincingly demonstrated that c-di-GMP does indeed have strong immunostimulatory properties. In vitro experiments have shown that c-di-GMP stimulates human immature dendritic cell (DC) expression of MHC class II, costimulatory molecules CD80/CD86 and maturation marker CD83, increases their secretion of cytokines and chemokines interleukin (IL)-12, interferon (IFN)-γ, IL-8, monocyte chemotactic protein 1 (MCP-1), IFN-γ inducible protein 10 (IP-10), and regulated on activation normal T cell expressed and secreted (RANTES), and alters expression of chemokine receptors including CCR1, CCR7 and CXCR4 [20]. Also, c-di-GMP-matured DCs demonstrated enhanced T cell stimulatory activity [20]. More importantly, the immunostimulatory properties of c-di-GMP have also been demonstrated in vivo. Intraperitoneal (i.p.