Given their safe use in humans and inherent adjuvanticity， Lactic Acid Bacteria may offer several advantages over other mucosal delivery strategies for cancer vaccines. The objective of this study is to evaluate the immune responses in mice after oral immunization with Lactobacillus (L) plantarum WCFS1 expressing a cell-wall anchored tumor antigen NY-ESO-1. And to investigate the immunostimulatory potency of this new candidate vaccine on human dendritic cells (DCs). L. plantarum displaying NY-ESO-1 induced NY-ESO-1 specific antibodies and T-cell responses in mice. By contrast， L. plantarum displaying conserved proteins such as heat shock protein-27 and galectin-1， did not induce immunity， suggesting tha... More
Given their safe use in humans and inherent adjuvanticity， Lactic Acid Bacteria may offer several advantages over other mucosal delivery strategies for cancer vaccines. The objective of this study is to evaluate the immune responses in mice after oral immunization with Lactobacillus (L) plantarum WCFS1 expressing a cell-wall anchored tumor antigen NY-ESO-1. And to investigate the immunostimulatory potency of this new candidate vaccine on human dendritic cells (DCs). L. plantarum displaying NY-ESO-1 induced NY-ESO-1 specific antibodies and T-cell responses in mice. By contrast， L. plantarum displaying conserved proteins such as heat shock protein-27 and galectin-1， did not induce immunity， suggesting that immune tolerance to self-proteins cannot be broken by oral administration of L. plantarum. With respect to immunomodulation， immature DCs incubated with wild type or L. plantarum-NY-ESO-1 upregulated the expression of co-stimulatory molecules and secreted a large amount of interleukin (IL)-12， TNF-α， but not IL-4. Moreover， they upregulated the expression of immunosuppressive factors such as IL-10 and indoleamine 2，3-dioxygenase. Although L. plantarum-matured DCs expressed inhibitory molecules， they stimulated allogeneic T cells in-vitro. Collectively， the data indicate that L. plantarum-NY-ESO-1 can evoke antigen-specific immunity upon oral administration and induce DC maturation， raising the potential of its use in cancer immunotherapies.
