Difference of T cell and B cell activation in two homologous proteins with similar antigenicity but great distinct immunogenicity
Autor: | Shaowei Li, Chun-Xin Lin, Mun-Hon Ng, Xiao-lu Wu, Tong Cheng, Ningshao Xia, Ting Wu, Jun Zhang, Shan-Hai Ou |
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Rok vydání: | 2007 |
Předmět: |
Viral Hepatitis Vaccines
B-Lymphocytes Antigenicity T-Lymphocytes Immunogenicity T cell Immunology food and beverages Priming (immunology) Biology Lymphocyte Activation medicine.disease_cause Virology Epitope medicine.anatomical_structure Viral Envelope Proteins Hepatitis E virus Immunogenetics medicine Alum adjuvant Antigens Viral Molecular Biology B cell |
Zdroj: | Molecular Immunology. 44:3261-3266 |
ISSN: | 0161-5890 |
DOI: | 10.1016/j.molimm.2007.01.002 |
Popis: | The candidate particulate hepatitis E vaccine, HEV 239, has been shown to be an efficacious vaccine in primates, and clinical study to date shows it to be safe and immunogenic for humans. The antigenicity of HEV 239 is virtually identical to its N-terminal 26 amino acids truncated protein, E2, which is not particulate but soluble. However, HEV 239 is over 200 times more immunogenic than E2. In present study, several events underlying this dramatic immunogenicity difference have been addressed. (1) HEV 239 can efficiently evoke a vigorous and predominant T cell response while E2 cannot induce detectable T cell response; (2) the dominant T cell epitopes in HEV 239 are identified, and both are also contained integrally in E2; (3) priming mice with Th epitope peptide can partially rescue the weak immunogenicity of E2 in alum adjuvant and (4) HEV 239 but not E2 can induce significant antibody response in athymic mice, which indicates that HEV 239 can directly activate B cell more efficiently. These results contribute to a better understanding of the mechanisms involved in the significant high immunogenicity of particulate antigen and may provide knowledge for the rational design and development of future vaccines. |
Databáze: | OpenAIRE |
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