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. 2005 Aug 7;11(29):4583-6.
doi: 10.3748/wjg.v11.i29.4583.

Novel DNA vaccine based on hepatitis B virus core gene induces specific immune responses in Balb/c mice

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Novel DNA vaccine based on hepatitis B virus core gene induces specific immune responses in Balb/c mice

Yi-Ping Xing et al. World J Gastroenterol. .

Abstract

Aim: To investigate the immunogenicity of a novel DNA vaccine, pSW3891/HBc, based on HBV core gene in Balb/c mice.

Methods: A novel DNA vaccine, pSW3891/HBc, encoding HBV core gene was constructed using a vector plasmid pSW3891. Balb/c mice were immunized with either pSW3891/HBc or empty vector DNA via gene gun. IgG anti-HBc responses in mouse sera were demonstrated by ELISA. Specific cytotoxicity of cytotoxic T lymphocytes (CTLs) of mice was quantitatively measured by lactate dehydrogenase release assay.

Results: HBcAg was expressed effectively in 293T cell line transiently transfected with pSW3891/HBc. Strong IgG anti-HBc responses were elicited in mice immunized with pSW3891/HBc. The end-point titers of anti-HBc reached the highest 1:97,200, 4 wk after the third immunization. The specific CTL killing with the highest specific lysis reached 73.25% at effector:target ratio of 20:1 in mice that received pSW3891/HBc DNA vaccine.

Conclusion: pSW3891/HBc vaccination elicits specific anti-HBc response and induces HBc-specific CTL response in immunized Balb/c mice.

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Figures

Figure 1
Figure 1
Digestion of pSW3891/HBc. Marker: λ/Hind III; C6, C7: clone no.
Figure 2
Figure 2
In vitro HBc expression in pSW3891/HBc transiently transfected 293T cells. V: pSW3891; L: lysate; C6: pSW3891/HBc/C6; S: supernatant.
Figure 3
Figure 3
End-point titres of anti-HBc in sera of Balb/c mice immunized with pSW3891/HBc.
Figure 4
Figure 4
Specific cytotoxicity of splenocytes inBalb/c mice immunized with pSW3891/HBc.

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References

    1. Rahman F, Dahmen A, Herzog-Hauff S, Böcher WO, Galle PR, Löhr HF. Cellular and humoral immune responses induced by intradermal or intramuscular vaccination with the major hepatitis B surface antigen. Hepatology. 2000;31:521–527. - PubMed
    1. Davis HL, McCluskie MJ, Gerin JL, Purcell RH. DNA vaccine for hepatitis B: evidence for immunogenicity in chimpanzees and comparison with other vaccines. Proc Natl Acad Sci USA. 1996;93:7213–7218. - PMC - PubMed
    1. Kwissa M, Unsinger J, Schirmbeck R, Hauser H, Reimann J. Polyvalent DNA vaccines with bidirectional promoters. J Mol Med (Berl) 2000;78:495–506. - PubMed
    1. Riedl P, Stober D, Oehninger C, Melber K, Reimann J, Schirmbeck R. Priming Th1 immunity to viral core particles is facilitated by trace amounts of RNA bound to its arginine-rich domain. J Immunol. 2002;168:4951–4959. - PubMed
    1. Kwissa M, Lindblad EB, Schirmbeck R, Reimann J. Codelivery of a DNA vaccine and a protein vaccine with aluminum phosphate stimulates a potent and multivalent immune response. J Mol Med (Berl) 2003;81:502–510. - PubMed

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