Skip to main content
Log in

Consecutive immunization with recombinant fowlpox virus and plasmid DNA for enhancing cellular and humoral immunity

  • Basic Investigation
  • Published:
Chinese Journal of Cancer Research

Abstract

Objective: To investigate the influence of consecutive immunization on cellular and humoral immunity in mice. Methods: We evaluated a consecutive immunization strategy of priming with recombinant fowlpox virus vUTALG and boosting with plasmid DNA pcDNAG encoding HIV-1 capsid protein Gag. Results: In immunized mice, the number of CD +4 T cells from splenic lymphocytes increased significantly and the proliferation response of splenocytes to ConA and LPS elevated markedly and HIV-1-specific antibody response could be induced. Conclusion: Consecutive immunization could increase cellular and humoral immunity responses in mice.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Somogyi P, Frazier J, Skinner M A. Fowlpox virus host range restriction: gene expression.DNA replication, and morphogenesis in nonpermissive mammalian cells[J]. Virology 1993; 197: 439.

    Article  PubMed  CAS  Google Scholar 

  2. Moss. B. Poxvirus vectors: Cytoplasmic expression of transferred genes[J]. Curr Opin Genet Dev 1993; 3: 86.

    Article  PubMed  CAS  Google Scholar 

  3. Baxby D, E Paoletti. Potential use of non-replicating vectors as recombinant vaccines[J]. Vaccine 1992; 10.

  4. Larche M. Related Articles Specific immunotherapy[J]. Br Med Bull 2000; 56: 1019.

    Article  PubMed  CAS  Google Scholar 

  5. Apostolopoulos V, Plebanski M. (Related Articles?) The evolution of DNA vaccines[J]. Curr Opin Mol Ther 2000; 2: 441.

    PubMed  CAS  Google Scholar 

  6. Lu S, Arthos J, Montefiori DC, et al. Simian immunodeficiency virous DNA vaccine trial in macaques[J]. J Virol 1996; 70: 3978.

    PubMed  CAS  Google Scholar 

  7. Kenneth E, Ugen, Susan B, et al. DNA vaccination with HIV-1 expressing constructs elicits immune responses in humans[J]. Vaccine 1998; 16: 1818.

    Article  Google Scholar 

  8. Ramsay AJ, Kent SJ, Strugnell RA, et al. Genetic vaccination strategies for enhanced cellular, humoral and mucosal immunity[J]. Immunol 1999;171: 27.

    Article  CAS  Google Scholar 

  9. Chen CH, Wang TL, Ji H, et al. Recombinant DNA vaccines protect against tumors that are resistant to recombinant vaccinia vaccines containing the same gene[J]. Gene Ther 2001; 8:128.

    Article  PubMed  CAS  Google Scholar 

  10. Mandell G L, et al. HIV and the acquired immunodeficiency syndrome. In: Bennett J C. et al. ed. Cecil Textbook of Medicine, 20th ed, Philadelphia: WB Saunders Co. 1996; 1837.

    Google Scholar 

  11. Norman LLetvin. Progress in the development of an HIV-1 vaccine. Science 1998; 1875.

  12. Kent S J, Zhao A, Best S J, et al. Enhanced T-cell immunogenicity and protective efficacy of a human immunodeficiency virus type 1 vaccine regimen consisting of consecutive priming with DNA and boosting with recombinant fowlpox virus[J]. J Virol 1998 72:10180.

    PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Jin Ning-yi.

Additional information

Foundation item: This work was supported by the National Scientific Research Foundation for Excellent Young Scientist of China (No. 398251197).

Biography: Luo Kun(1966–), doctor of medicine, lecturer, now works at Institute of Immunology, Zhejiang University, majors in molecular immunology.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Luo, K., Jin, Ny., Guo, Zr. et al. Consecutive immunization with recombinant fowlpox virus and plasmid DNA for enhancing cellular and humoral immunity. Chin. J. Cancer Res. 13, 247–250 (2001). https://doi.org/10.1007/s11670-001-0040-x

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11670-001-0040-x

Key words

CLC number

Navigation