PPS nanoparticles as versatile delivery system to induce systemic and broad mucosal immunity after intranasal administration
Degradable polymer nanoparticles (NPs, 50nm) based on polypropylene sulfide (PPS) were conjugated to thiolated antigen and adjuvant proteins by reversible disulfide bonds and evaluated in mucosal vaccination. Ovalbumin was used as a model antigen, and antigen-conjugated NPs were administered intranasally in the mouse. We show penetration of nasal mucosae, transit via M cells, and uptake by antigen-presenting cells in the nasal-associated lymphoid tissue. Ovalbumin-conjugated NPs induced cytotoxic T lymphocytic responses in lung and spleen tissues, as well as humoral response in mucosal airways. Co-conjugation of the TLR5 ligand flagellin further enhanced humoral responses in the airways as well as in the distant vaginal and rectal mucosal compartments and induced cellular immune responses with a Th1 bias, in contrast with free flagellin. The PPS NP platform thus appears interesting as a platform for intranasally-administered mucosal vaccination for inducing broad mucosal immunity.
Keywords: Mucosal vaccine ; Nanoparticles ; Flagellin ; Cytotoxic T lymphocytes ; Gram-Negative Flagellin ; Dendritic Cells ; Protective Immunity ; Adjuvant Activity ; Vaccines ; Immunization ; Proteins ; Antigen ; Salmonella ; Activation
Record created on 2010-12-03, modified on 2016-08-09