Title

Efficient mucosal vaccination mediated by the neonatal Fc receptor.

Document Type

Article

Publication Date

2011

Keywords

Animals, Cell-Line, Cytokines, Female, Flow-Cytometry, Histocompatibility-Antigens-Class-I, Immunoglobulin-G, Kaplan-Meier-Estimate, Mice-Knockout, Molecular-Targeted-Therapy, Mucous-Membrane, Receptors-Fc, Recombinant-Fusion-Proteins, Vaccines, Vagina, Viral-Envelope-Proteins

JAX Source

Nat Biotechnol 2011 Feb; 29(2):158-63.

Abstract

Almost all infectious diseases are initiated at mucosal surfaces, yet intramuscular or subcutaneous vaccination usually provides only minimal protection at sites of infection owing to suboptimal activation of the mucosal immune system. The neonatal Fc receptor (FcRn) mediates the transport of IgG across polarized epithelial cells lining mucosal surfaces. We mimicked this process by fusing a model antigen, herpes simplex virus type-2 (HSV-2) glycoprotein gD, to an IgG Fc fragment. Intranasal immunization, together with the adjuvant CpG, completely protected wild-type, but not FcRn knockout, mice after intravaginal challenge with virulent HSV-2 186. This immunization strategy induced efficient mucosal and systemic antibody, B- and T-cell immune responses, with stable protection for at least 6 months after vaccination in most of the immunized animals. The FcRn-IgG transcellular transport pathway may provide a general delivery route for subunit vaccines against many mucosal pathogens.

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