A more sophisticated strategy

that is evolving, is to target several different but key proteins in the chlamydial repertoire. Chlamydia has evolved over its long history to have multiple mechanisms of infecting and controlling its host and hence a vaccine that does not rely on a single target has the best chance of success. To this end, the concept of targeting several surface proteins (such as MOMP, Pmps, Incs) as well as some internal or secreted regulatory proteins (such as CPAF, NrdB) has significant merit ( Fig. 1 (a) summarizes the antigens related to each stage of the chlamydial developmental cycle, and Table 2 shows how these might be combined effectively in this website multi-antigen vaccines). GSK1120212 nmr In addition, specifically targeting antigens that are more highly expressed in the persistent or chronic

phase of infection/disease, has considerable merit. While the major goal of a chlamydial vaccine is to prevent infection in naive individuals, it may not be possible to screen all vaccinees to ensure they are negative prior to vaccination. In addition, if sterilizing immunity is difficult or impossible to achieve, then including persistence phase antigens in a vaccine would have significant merit. Such multi-target vaccines are well within the reach of current technologies and clearly are successful with other infectious disease vaccines, such as meningococcal disease vaccines. All candidate antigens though require effective adjuvants and the optimal delivery mechanism to be an effective vaccine. The challenge with a C. trachomatis STI vaccine is that the vaccine-adjuvant combination must elicit Suplatast tosilate the correct balance of Th2 (neutralizing antibodies) and Th1 (IFN-g and Th17 cytokines) responses and it must do this at the required mucosal sites (female genital tract). Thanks to recent progress

in vaccinology and immunology more broadly, the range of adjuvants that are now available, and well advanced in human safety trials [89] is rapidly increasing and some promising results with C. trachomatis vaccines are emerging. The range of adjuvants and delivery systems that have been evaluated with C. trachomatis vaccines include immunostimulating complexes [88] and [90], detergent/surfactant-based adjuvants [91], live viral vectors [92], Vibrio cholerae ghosts [93], liposomes [ [94], CpG and their more recently developed, safe derivatives [88] and cytokines. One challenge for chlamydial vaccine development is whether it should (i) primarily aim to significantly reduce or even eliminate the infection, or (ii) should also, or perhaps only, aim to reduce or eliminate the adverse pathology, in particular upper genital tract pathology in females.