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Vaccine2010; 29(2); 212-220; doi: 10.1016/j.vaccine.2010.10.053

Induction of neutralizing antibodies to Hendra and Nipah glycoproteins using a Venezuelan equine encephalitis virus in vivo expression system.

Abstract: The emergence of Hendra Virus (HeV) and Nipah Virus (NiV) which can cause fatal infections in both animals and humans has triggered a search for an effective vaccine. Here, we have explored the potential for generating an effective humoral immune response to these zoonotic pathogens using an alphavirus-based vaccine platform. Groups of mice were immunized with Venezuelan equine encephalitis virus replicon particles (VRPs) encoding the attachment or fusion glycoproteins of either HeV or NiV. We demonstrate the induction of highly potent cross-reactive neutralizing antibodies to both viruses using this approach. Preliminary study suggested early enhancement in the antibody response with use of a modified version of VRP. Overall, these data suggest that the use of an alphavirus-derived vaccine platform might serve as a viable approach for the development of an effective vaccine against the henipaviruses.
Publication Date: 2010-11-02 PubMed ID: 21050901PubMed Central: PMC3032421DOI: 10.1016/j.vaccine.2010.10.053Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • N.I.H.
  • Extramural

Summary

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This study highlights a potential strategy for creating an effective vaccine against Hendra and Nipah viruses by using a vaccine platform derived from Venezuelan equine encephalitis virus.

Objective of the Research

  • The primary goal of this research was to pave the way for an effective vaccine against the Hendra Virus (HeV) and the Nipah Virus (NiV). Both these viruses can cause fatal infections in animals and humans and hence finding a reliable prophylactic measure is essential.

Methodology & Findings

  • The researchers employed an alphavirus-based vaccine platform for this purpose. Specifically, they used Venezuelan equine encephalitis virus replicon particles (VRPs), which were engineered to express HeV and NiV attachment or fusion glycoproteins.
  • These VRPs were then used to immunize groups of mice. The results exhibited a successful induction of robust neutralizing antibodies capable of responding to both HeV and NiV. In immunology, ‘neutralizing antibodies’ refer to those that not only recognize a pathogen but can also block its harmful effects, thus providing immunity.
  • Furthermore, preliminary investigations hinted at an enhanced antibody response with the usage of modified VRPs, suggesting potential improvements in vaccine efficacy.

Conclusion

  • This study’s success potentially indicates that an alphavirus-based vaccine platform could be a promising pathway for procuring an effective vaccine against the henipaviruses (a family of viruses that include Hendra and Nipah Viruses).
  • However, even though these are significant findings, they’re relatively preliminary. More clinical trials testing this vaccine strategy on different animal models and, eventually, in humans, are necessary to prove the safety and efficacy before its dissemination for public use.

Cite This Article

APA
Defang GN, Khetawat D, Broder CC, Quinnan GV. (2010). Induction of neutralizing antibodies to Hendra and Nipah glycoproteins using a Venezuelan equine encephalitis virus in vivo expression system. Vaccine, 29(2), 212-220. https://doi.org/10.1016/j.vaccine.2010.10.053

Publication

ISSN: 1873-2518
NlmUniqueID: 8406899
Country: Netherlands
Language: English
Volume: 29
Issue: 2
Pages: 212-220

Researcher Affiliations

Defang, Gabriel N
  • Department of Preventive Medicine and Biometrics, Uniformed Services University of the Health Sciences, 4301 Jones Bridge Road, Bethesda, MD 20814, USA. gabriel.defang@med.navy.mil
Khetawat, Dimple
    Broder, Christopher C
      Quinnan, Gerald V

        MeSH Terms

        • Animals
        • Antibodies, Neutralizing / blood
        • Antibodies, Viral / blood
        • Encephalitis Virus, Venezuelan Equine / genetics
        • Female
        • Gene Expression
        • Genetic Vectors
        • Hendra Virus / genetics
        • Hendra Virus / immunology
        • Henipavirus Infections / immunology
        • Henipavirus Infections / prevention & control
        • Mice
        • Mice, Inbred C3H
        • Nipah Virus / genetics
        • Nipah Virus / immunology
        • Vaccines, Synthetic / genetics
        • Vaccines, Synthetic / immunology
        • Viral Proteins / genetics
        • Viral Proteins / immunology

        Grant Funding

        • AI037438 / NIAID NIH HHS
        • AI054715 / NIAID NIH HHS
        • U54 AI057168 / NIAID NIH HHS
        • R01 AI054715 / NIAID NIH HHS
        • AI057168 / NIAID NIH HHS
        • R21 AI037438 / NIAID NIH HHS
        • R01 AI037438 / NIAID NIH HHS

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