Description
The goal of this study was to identify the transcriptional mechanisms involved in the activation of the immune system by QS-21, a triterpene glycoside purified from the bark of Quillaja saponaria which has adjuvant activity in vivo. Saponins represent a promising class of vaccine adjuvant. Together with the TLR4-ligand MPL, QS-21 is  part of the Adjuvant System AS01, a key component of the Malaria and Zoster candidate vaccines that  display demonstrated clinical efficacy. However, the mechanism of action of QS-21 in this liposomal  formulation is poorly understood. Upon intra-muscular immunisation, we observed that QS-21 rapidly  accumulated in CD169+ resident macrophages of the draining lymph node where it elicited a local  innate immune response. Depletion of these cells abrogated QS-21-mediated innate cell recruitment  to the lymph node, dendritic cell (DC) phenotypic maturation as well as the adjuvant effect on T cell and  antibody responses to co-administered antigens. DCs rather than lymph node-resident macrophages  were directly involved in T cell priming by QS-21 as revealed by the decrease in antigen-specific T cell  response in Batf3/ mice. Further analysis showed that the adjuvant effect of QS-21 depended on the  integration of Caspase-1 and MyD88 pathways, at least in part through the local release of HMGB1.  Taken together, this work unravels the key role of lymph node sentinel macrophage in controlling the  adjuvant effect of a molecule proven to improve vaccine response in humans