“…Nevertheless, today, it is known that innate immune cells, especially dendritic cells (DCs), which are the major antigen-presenting cells (APCs), can sense pathogen- and damage-associated molecular patterns (PAMP and DAMP, respectively) by different receptors (such as TLR, NOD- and RIG-like receptors). Many of these molecules, which could be part of adjuvants or components released from injured or dying cells on the site of the vaccine injection, induce inflammation, activate DCs and induce adaptive immunity mediated by vaccine antigen-specific T and B lymphocytes [ 10 , 11 , 12 , 13 , 14 ]. Briefly, during the recognition of vaccine antigens presented on DCs by the CD4+ T helper (Th) cell, DC-derived cytokines and costimulatory molecules on their cell surface influence Th cell differentiation towards three major subsets called Th1, Th2 and Th17 [ 10 ].…”