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©2007 Baishideng Publishing Group Co.
World J Gastroenterol. Nov 28, 2007; 13(44): 5911-5917
Published online Nov 28, 2007. doi: 10.3748/wjg.v13.i44.5911
Published online Nov 28, 2007. doi: 10.3748/wjg.v13.i44.5911
Figure 1 A: Comparison of T cell proliferation between different groups after stimulation with HBV protein (C57BL/6 mice); B: Comparison of T cell proliferation between stimulation with HBV protein and with non-related protein (Balb/c mice); C: Comparison of CTL activity to HBV protein pulsed target cells between different groups (C57BL/6 mice).
Figure 2 A: Comparison of T cell proliferation between different groups after stimulation with HBV classIpeptide (C57BL/6 mice); B: Comparison of CTL activity to HBV classIpeptide pulsed target cells between different groups (C57BL/6 mice); C: Comparison of T cell proliferation between stimulation with HBV and with non-related classI peptide (Balb/c mice); D: Comparison of CTL activity to HBV classIpeptide pulsed target cell between HBV and non-related classIpeptide (Balb/c mice).
Figure 3 A: Comparison of T cell proliferation between different groups after stimulation with HBV class II peptide (C57BL/6 mice); B: Comparison of T cell proliferation after stimulation with different class II peptide (Balb/c mice).
Figure 4 Comparison of CTL activity to target cells pulsed with different agents (Balb/c mice).
Figure 5 Comparison of antibody titers to HBV between different groups after immunization (Balb/c mice).
Figure 6 A: Tumor incidence after CT26-HBeAg challenge of Balb/c mice; B: Tumor growth after CT26-HBeAg challenge of Balb/c mice.
- Citation: Gu QL, Huang X, Ren WH, Shen L, Liu BY, Chen SY. Targeting hepatitis B virus antigens to dendritic cells by heat shock protein to improve DNA vaccine potency. World J Gastroenterol 2007; 13(44): 5911-5917
- URL: https://www.wjgnet.com/1007-9327/full/v13/i44/5911.htm
- DOI: https://dx.doi.org/10.3748/wjg.v13.i44.5911