AI Article Synopsis

  • Bovine Viral Diarrhoea Virus (BVDV) leads to significant economic losses in the cattle industry, prompting research into improved subunit vaccines based on the immunogenic glycoprotein E2.
  • A novel hollow silica vesicle (SV-140) platform has been created to deliver the optimized E2 antigen as a nanovaccine, showing effectiveness in inducing long-term immune responses in small animal models.
  • The study indicates that the oE2/SV-140 formulations provide sustained immunity and minimal side effects, suggesting potential for single-dose vaccines that do not require cold storage for broader use in veterinary and human medicine.

Article Abstract

Bovine Viral Diarrhoea Virus (BVDV) is one of the most serious pathogen, which causes tremendous economic loss to the cattle industry worldwide, meriting the development of improved subunit vaccines. Structural glycoprotein E2 is reported to be a major immunogenic determinant of BVDV virion. We have developed a novel hollow silica vesicles (SV) based platform to administer BVDV-1 Escherichia coli-expressed optimised E2 (oE2) antigen as a nanovaccine formulation. The SV-140 vesicles (diameter 50 nm, wall thickness 6 nm, perforated by pores of entrance size 16 nm and total pore volume of 0.934 cm3 g(-1)) have proven to be ideal candidates to load oE2 antigen and generate immune response. The current study for the first time demonstrates the ability of freeze-dried (FD) as well as non-FD oE2/SV140 nanovaccine formulation to induce long-term balanced antibody and cell mediated memory responses for at least 6 months with a shortened dosing regimen of two doses in small animal model. The in vivo ability of oE2 (100 μg)/SV-140 (500 μg) and FD oE2 (100 μg)/SV-140 (500 μg) to induce long-term immunity was compared to immunisation with oE2 (100 μg) together with the conventional adjuvant Quil-A from the Quillaja saponira (10 μg) in mice. The oE2/SV-140 as well as the FD oE2/SV-140 nanovaccine generated oE2-specific antibody and cell mediated responses for up to six months post the final second immunisation. Significantly, the cell-mediated responses were consistently high in mice immunised with oE2/SV-140 (1,500 SFU/million cells) at the six-month time point. Histopathology studies showed no morphological changes at the site of injection or in the different organs harvested from the mice immunised with 500 μg SV-140 nanovaccine compared to the unimmunised control. The platform has the potential for developing single dose vaccines without the requirement of cold chain storage for veterinary and human applications.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4668082PMC
http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0143507PLOS

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Article Synopsis
  • Bovine Viral Diarrhoea Virus (BVDV) leads to significant economic losses in the cattle industry, prompting research into improved subunit vaccines based on the immunogenic glycoprotein E2.
  • A novel hollow silica vesicle (SV-140) platform has been created to deliver the optimized E2 antigen as a nanovaccine, showing effectiveness in inducing long-term immune responses in small animal models.
  • The study indicates that the oE2/SV-140 formulations provide sustained immunity and minimal side effects, suggesting potential for single-dose vaccines that do not require cold storage for broader use in veterinary and human medicine.
View Article and Find Full Text PDF

Bovine Viral Diarrhoea Virus (BVDV) is widely distributed in cattle industries and causes significant economic losses worldwide annually. A limiting factor in the development of subunit vaccines for BVDV is the need to elicit both antibody and T-cell-mediated immunity as well as addressing the toxicity of adjuvants. In this study, we have prepared novel silica vesicles (SV) as the new generation antigen carriers and adjuvants.

View Article and Find Full Text PDF

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