This study demonstrated that sublingual immunization with a fusion protein, 25k‐hagA‐MBP, which consists of a 25‐kDa antigenic region of hemagglutinin A purified from Porphyromonas gingivalis fused to maltose‐binding protein (MBP) originating from Escherichia coli as an adjuvant, elicited protective immune responses. Immunization with 25k‐hagA‐MBP induced high levels of antigen‐specific serum IgG and IgA, as well as salivary IgA. High level titers of serum IgG and IgA were also induced for almost 1 year. In an IgG subclass analysis, sublingual immunization with 25k‐hagA‐MBP induced both IgG1 and IgG2b antibody responses. Additionally, numerous antigen‐specific IgA antibody‐forming cells were detected from the salivary gland 7 days after the final immunization. Mononuclear cells isolated from submandibular lymph nodes (SMLs) showed significant levels of proliferation upon restimulation with 25k‐hagA‐MBP. An analysis of cytokine responses showed that antigen‐specific mononuclear cells isolated from SMLs produced significantly high levels of IL‐4, IFN‐γ, and TGF‐β. These results indicate that sublingual immunization with 25k‐hagA‐MBP induces efficient protective immunity against P. gingivalis infection in the oral cavity via Th1‐type and Th2‐type cytokine production.