Sublingual vaccination with fusion protein consisting of the functional domain of hemagglutinin A of Porphyromonas gingivalis and Escherichia coli maltose-binding protein elicits protective immunity in the oralcavity.
Sublingual vaccination with fusion protein consisting of the functional domain of hemagglutinin A of Porphyromonas gingivalis and Escherichia coli maltose-binding protein elicits protective immunity in the oralcavity.
复制标题
舌下接种由牙龈卟啉单胞菌血凝素 A 功能域和大肠杆菌麦芽糖结合蛋白组成的融合蛋白,可在口腔中引发保护性免疫。
DOI:
10.1111/j.1574-695x.2011.00895.x
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发表时间:
2012
期刊:
影响因子:
--
通讯作者:
Yamamoto M.
中科院分区:
文献类型:
--
作者:
Yuzawa S;Kurita-Ochiai T;Hashizume T,Kobayashi R;Abiko Y;Yamamoto M.
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 fromPorphyromonas gingivalisfused to maltose-binding protein (MBP) originating fromEscherichia colias 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 againstP. gingivalisinfection in the oral cavity via Th1-type and Th2-type cytokine production.