Priming with an HEV Th epitope can improve the humoral immunogenicity of its native protein.
- Author:
Chun-Xin LIN
1
;
Ting WU
;
Xiao-Lu WU
;
Ming-Hui XIE
;
Tong CHENG
;
Shao-Wei LI
;
Jun ZHANG
;
Ning-Shao XIA
Author Information
1. National Institute of Diagnostics and Vaccine Development in Infectious Disease, Xiamen University, Xiamen 361005, China.
- Publication Type:Journal Article
- MeSH:
Animals;
Antibodies, Viral;
blood;
immunology;
Cell Proliferation;
Cell Survival;
immunology;
Enzyme-Linked Immunosorbent Assay;
Epitopes;
immunology;
Female;
Flow Cytometry;
Hepatitis E virus;
immunology;
Immunization;
methods;
Immunization, Secondary;
Interferons;
metabolism;
Mice;
Mice, Inbred BALB C;
Spleen;
cytology;
immunology;
metabolism;
T-Lymphocytes;
cytology;
immunology;
metabolism;
Viral Vaccines;
administration & dosage;
immunology
- From:
Chinese Journal of Biotechnology
2007;23(2):310-314
- CountryChina
- Language:Chinese
-
Abstract:
A dominant H-2d restricted Th epitope P34 was found to be contained in recombinant particulate hepatitis E virus (HEV) vaccine HEV 239. In this paper, the cellular immune response induced in P34 immunized BALB/c mice were studied and the priming effect of P34 was characterized. Groups of BALB/c mice were subcutaneously (s. c.) immunized with P34, splenocytes were then stimulated with P34 and HEV 239 protein, cellular immune response was assayed by IFN-gamma-ELISPOT, flow cytometry and T cell proliferation experiments. Results showed that P34 immunized BALB/c splenocytes responsed to P34 and HEV 239 protein stimulation in IFN-gamma-ELISPOT, flow cytometry and T cell proliferation experiments. After depletion of the CD4+ T cells from the immunized splenocytes by magnetic separation, the response decreased to the background level while almost no influence was observed after CD8 + T cells depletion which showed that the cells responsible for IFN-gamma secretion were mainly CD4+ T cells. Then mice were primed with P34 and boosted with its vector protein, E2, the E2 specific antibody titer were assayed. Results showed that after P34 priming, some of the 10 microg, 20 microg E2 boosted mice could develop anti-E2 antibody 1 week later and all the mice had detectable antibody 3 weeks after boosting. In the control peptide P18 priming group, even after boosting with 20 microg E2, anti-E2 antibody couldn't be detected until the end of this experiment. The results showed that priming with P34 epitope could increase the immunogenicity of its vector protein, E2, in BALB/c mice.
