In this issue, Van Roey et al. [Eur. J. Immunol. 2012. 42: 353–363] explore one of these challenges, namely to identify novel mucosal adjuvants. see more Van Roey

et al. show that the pro-allergic cytokine thymic stromal lymphopoietin (TSLP) promotes a strong B-cell response with production of secretory IgA at mucosal sites. Here, we discuss the importance and limits of these findings within the broader field of vaccine adjuvants, and the potential development of TSLP as a mucosal and B-cell adjuvant in humans. Adjuvants are critical components of vaccine formulations, required to induce an appropriate and protective immune response 1. They can be defined as molecules acting independently of an

antigen in order to directly activate innate and/or adaptive immune cells. They can promote humoral or cellular immunity, influence the cytokine polarity of T-helper (Th) cell responses, and modulate the effector T (Teff)-versus Treg-cell balance. In addition, they may promote a local or systemic immune response. Most vaccines are administered systemically, by sub-cutaneous or intra-muscular routes, and induce a systemic immune response, measured by the serum Ab titer. Circulating IgG may also contribute to the local immune response at mucosal surfaces, but with reduced efficiency as compared with secretory IgA (sIgA). Given that many pathogens are acquired through mucosal infection, efforts have been made to this website specifically induce sIgA at mucosal surfaces. To this end, the mucosal route of immunization appears to be a superior way of inducing both an imprint of adaptive immune cells 2, and the expression of homing molecules directing Teff and B cells to the mucosa

3. Currently, at least six vaccines have been approved for mucosal administration, mostly oral. These include vaccines against cholera, Salmonella typhimurium, influenza, polio virus, and rotavirus 4. Vaccine formulations contain live, attenuated, or inactivated microbial strains. The further development of mucosal vaccines is, however, limited by the lack of specific adjuvants that are necessary to promote strong mucosal immunity and the production of secretory IgA in response Cobimetinib concentration to large variety of antigens, and to avoid the risk of inducing oral tolerance 4. In the past decade, most attention in the vaccine field has been placed on innate adjuvants that trigger pattern recognition receptors, such as TLRs 5, 6. A large number of synthetic or natural TLR ligands are being explored as adjuvants in pre-clinical or clinical studies 7, 8. Although CpG oligonucleotides can be used in mucosal immunization protocols 9, this strategy has not been greatly explored. Other TLR ligands are used systemically or injected locally in tumors in order to promote innate immune activation at the site of antigenic challenge 7.