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[Combination immunization with EIAV Env protein expressed by recombinant baculovirus and recombinant vaccinia virus containing env gene].

Abstract: To develop a novel vaccine candidate of Equine infectious anemia virus(EIAV). Methods: env genes of EIAV Chinese donkey leukocyte attenuated strain (EIAV DLV) and its parental virus strain (EIAV LN) were expressed using the BAC-To-BAC system, and Env proteins were confirmed by SDS-PAGE and Western blot. BALB/c mice were immunized with recombinant vaccinia viruses containing env genes of EIAV alone or boosted with Env proteins expressed by recombinant baculovirus. Both protective humoral and cellular immune responses were detected. Results: Recombinant baculovirus could express complete Env proteins and the titer of neutralizing antibody in the prime-boost group was found to be 5 to 9 folds higher than that in the rVV group. Conclusions: Combination of protein antigen and recombinant vaccinia virus could induce high titer of neutralizing antibody against EIAV. This work facilitates development of a novel genetically engineered vaccine of EIAV as a model for future development of an HIV vaccine.
Publication Date: 2004-06-23 PubMed ID: 15207082
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  • English Abstract
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

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The study aims to develop a new type of vaccine for Equine Infectious Anemia Virus (EIAV) and analyzes the impact of combining protein antigen and recombinant vaccinia virus to produce a higher neutralizing antibody rate. This research could potentially benefit the development of HIV vaccines in the future.

Research Methodology

  • For developing an innovative vaccine candidate to combat the Equine infectious anemia virus (EIAV), researchers selected the Env genes from two strains: EIAV Chinese donkey leukocyte attenuated strain (EIAV DLV) and its parental virus strain (EIAV LN).
  • With the help of the BAC-To-BAC system, these Env genes were expressed, and the presence of the Env proteins was confirmed using SDS-PAGE and Western blot methods.
  • BALB/c mice were used as a model for the immunization process. They were administered with recombinant vaccinia viruses in which the env genes of EIAV were present, either alone or enhanced with Env proteins expressed via recombinant baculovirus.
  • Afterward, the humoral and cellular immune responses in the mice were studied, contributing to the evidence of protective immune reactions.

Research Findings

  • The use of recombinant baculovirus effectively led to the production of complete Env proteins. This was a significant step forward in the vaccine development.
  • The study found that the titer of neutralizing antibody in the prime-boost group was significantly higher – between 5 to 9 times – than the rVV group. This indicates that combining the protein antigen with recombinant vaccinia virus can generate a stronger immune response against the EIAV.

Research Implications

  • These findings suggest that a combination of protein antigen and recombinant vaccinia virus could lead to an effective vaccine strategy to induce higher rates of neutralizing antibodies against EIAV.
  • This study could potentially pave the way for the development of a novel genetically engineered vaccine against EIAV. The impacts of this research are not limited to EIAV alone but may inform future advancements in developing an effective vaccine strategy for HIV.

Cite This Article

APA
Dai CM, Zhang XY, Zhang RR, Shao YM, Shen RX. (2004). [Combination immunization with EIAV Env protein expressed by recombinant baculovirus and recombinant vaccinia virus containing env gene]. Xi Bao Yu Fen Zi Mian Yi Xue Za Zhi, 20(4), 410-414.

Publication

ISSN: 1007-8738
NlmUniqueID: 101139110
Country: China
Language: chi
Volume: 20
Issue: 4
Pages: 410-414

Researcher Affiliations

Dai, Chun-ming
  • Division of Research on Virology and Immunology, National Center for AIDS/STD Control and Prevention, CDC, Beijing 100050, China. dcmzd@hotmail.com
Zhang, Xiao-yan
    Zhang, Ran-ran
      Shao, Yi-ming
        Shen, Rong-xian

          MeSH Terms

          • Animals
          • Antibody Formation
          • Baculoviridae / genetics
          • Cells, Cultured
          • Female
          • Gene Products, env / biosynthesis
          • Gene Products, env / genetics
          • Gene Products, env / immunology
          • Genes, env
          • Immunity, Cellular
          • Immunization
          • Infectious Anemia Virus, Equine / genetics
          • Infectious Anemia Virus, Equine / immunology
          • Mice
          • Mice, Inbred BALB C
          • Recombination, Genetic
          • Spodoptera / cytology
          • Spodoptera / metabolism
          • Transfection
          • Vaccines, DNA / biosynthesis
          • Vaccines, DNA / immunology
          • Vaccinia virus / genetics

          Citations

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