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        Cytokine and Costimulatory Factor-Encoding Plasmids as Adjuvants for DNA Vaccination

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        The induction of a potent and long-lasting immunity is one of the most important elements to consider in developing an effective vaccine. DNA vaccines induce markedly stronger CD8+ cytotoxic T lymphocyte (CTL) activity than do traditional peptide vaccines through their particular mechanism of antigen presentation mediated by MHC class I molecules. Induction of CTL specific to pathogenic viruses is thought to provide a reliable means of protecting a host from infection and halting disease progression, as these cells can directly recognize and lyse infected cells. However, in most of the early studies showing induction of pathogen-specific CTL, antigen-encoding immunogenic DNA alone was used and DNA vectors encoding immunomodulating molecules were not considered. It now appears that various types of immunomodulatory molecules such as cytokines (IL-1 [1 ], IL-2 [2 ], IL-12 [3 ], IFN-γ [4 ], IL-7 [5 7 ], and GM-CSF [8 ,9 ]), chemokines (TCA-3 [10 ], RANTES [11 ], MIP-1 [11 ]), and costimulatory molecules (CD40L [12 ], B7-1 [13 ] and B7-2 [14 ]) could enhance or modify the specific immune responses elicited by DNA immunization (see Table 1 ).
        Table 1  Summary of Effects of Cytokines after Conventional Vaccination and of Expression Plasmids following DNA Immunization

        Immunomodulatory Molecules

        Effect

         

        Ref.

        A. Cytokine proteins

             

        IL-1

        Antibody (Ab)

        (23 ,24 )

        IL-2

        Ab

        (2 ,25 ,26 )

        IL-12

        TH1(DTH)

        (3 )

        IFN-γ

        Ab, DTH

        (4 ,25 ,27 )

        GM-CSF

        Ab

        (28 ,29 )

        B. Expression plasmids

             

        IL-12

        CTL

        ↑(i.m. and i.n.)

        (15 ,21 ,22 ,30 )

         

        DTH

        ↑(i.m. and i.n.)

        (5 ,21 )

         

        Ab

        →(i.m. and i.n.)

        (15 ,22 )

        GM-CSF

        Ab

        ↑(i.m.)

        (9 ,18 ,22

         

        CTL

        ↑(i.m.)

        (18 )

         

        3 H-TdR uptake

        ↑(i.m.)

        (9 )

        TCA3

        CTL

        ↑(i.m.)

        (31 )

         

        DTH

        ↑(i.m.)

        (31 )

         

        Ab

        →(i.m.)

        (31 )

        B7-1

        CTL

        →(i.m.)

        (19 )

         

        DTH

        →(i.m.)

        (19 )

         

        Ab

        →(i.m.)

        (19 )

        B7-2

        CTL

        ↑(i.m.)

        (19 )

         

        DTH

        ↑(i.m.)

        (19 )

         

        Ab

        →(i.m.)

        (19 )

        CD40(L)

             
         

        Ab

        →(i.m.)

        (A. Ihata et al., Unpublished data)

         

        CTL

        ↑(i.m.)

        (A. Ihata et al., Unpublished data)

        i.m., intramuscular administration; i.n., intranasal administration; Ab, antibody production; DTH, delayed type hypersensitivity; 3 H-TdR, incorporation of 3 H-Thymidine; ↑, activated immune response.
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