Rift Valley Fever
Solutions
Online Inquiry

Rift Valley Fever

Rift Valley fever (RVF), predominantly found in sub-Saharan Africa and the Arabian Peninsula, poses a significant threat to both livestock and human health, with potentially fatal consequences for the latter. In response to this challenge, our company provides an extensive range of specialized services designed to expedite the advancement of RVF vaccines and therapeutics.

Overview of Rift Valley Fever

Rift Valley fever (RVF), a mosquito-borne illness stemming from the Rift Valley fever phlebovirus (RVFV), emerged in Kenya in the early 1900s. This disease has led to recurrent epidemics, exerting profound adverse effects on animal husbandry and human well-being. Typically transmitted through mosquito vectors, RVF can also be contracted through contact with infected animal matter. It often results in high newborn mortality rates and pregnancy losses in livestock, while in humans, it can present with a spectrum of symptoms from fever to serious conditions such as meningoencephalitis, retinitis, and hemorrhagic fever.

Schematic illustration of RVFV genome organization.Fig.1 Schematic illustration of Rift Valley fever phlebovirus (RVFV) genome organization. (Faburay B., et al., 2017)

Vaccine Development for Rift Valley Fever

  • Subunit and Recombinant Protein Vaccines: These vaccines focus on critical viral antigens like the glycoproteins Gn and Gc. An example includes the development of a baculovirus-expressed RVFV glycoprotein subunit vaccine that demonstrated robust neutralizing responses in sheep models.
  • DNA and Viral Vectored Vaccines: Utilizing recombinant nucleic acid technology, DNA vaccines encoding RVFV antigens have shown promise in preclinical trials. Similarly, viral vector vaccines that deliver RVFV antigens using harmless viral carriers are under investigation.
  • Virus-Like Particles (VLPs): VLPs mimic the native virus structure, stimulating an immune response without containing viral genetic material. VLP-based vaccines are considered safe and effective, with examples like the RVFV VLPs showing potential in preclinical studies.
  • DIVA-Compliant Vaccines: Differentiating Infected from Vaccinated Animals (DIVA) is crucial for trade and disease surveillance. The development of such vaccines allows for antibodies against RVFV to be distinguished based on their specificity.

Table 1 Status of Rift Valley fever vaccines and vaccine candidates evaluated in different animal models. (Faburay B., et al., 2017)

Type of Vaccine Host Species Evaluated/Used in DIVA (differentiating infected from vaccinated animals)
Mice Sheep Cattle NHP Other
Inactivated
NDBR103       √ (Human volunteers) No
TSI GSD 200         √ (Human volunteers) No
Formalin inactivated (Egypt)       No
Formalin Inactivated (South Africa)       No
Genetically non-modified-live
Smithburn     No
MP12 √ (Human volunteers) No
Genetically modified-live
Clone 13, Cl13T   √ (Human volunteers) Yes
R566         Yes
Recombinant ZH501 Δ/mutants       Yes
Recombinant MP12 Δ/mutants       Yes
Four-segmented RVFV       Yes
Recombinant protein vaccines     Yes
DNA vaccines         Yes
Virus-like particles (VLPs)         Yes
Virus replicons       Yes
Virus-vectored            
Poxviruses     Yes
Newcastle Disease Virus     Yes
Modified vaccinia Ankara     Yes
Chimpanzee adenovirus   √ (goats and camels) Yes
Equine herpesvirus virus type 1         Yes

Therapeutics Development for Rift Valley Fever

Ribavirin: As a broad-spectrum antiviral, ribavirin has shown in vitro activity against RVFV. However, in vivo efficacy has been limited due to side effects.

Favipiravir: This nucleotide analog has demonstrated significant efficacy against RVFV in preclinical studies, both as monotherapy and in combination with ribavirin.

Host-Targeted Therapies: Given the broad range of cellular processes exploited by RVFV, therapies targeting host factors are being explored. This includes the use of proteasome inhibitors like bortezomib, which modulate the cellular environment to impair viral replication.

Our Services

Vaccine Design and Development: We specialize in creating novel vaccine candidates, leveraging cutting-edge technologies such as recombinant protein expression and VLP production.

Antiviral Drug Discovery: Our team employs high-throughput screening to identify potential antiviral compounds, followed by rigorous optimization for efficacy and safety.

We conduct comprehensive in vitro evaluations to assess the efficacy of vaccine and drug candidates against RVFV. In addition, detailed analysis of immune responses post-vaccination and the impact of therapeutics on viral loads are core components of our preclinical research. If you are interested in our services, please feel free to contact us.

References

  1. Faburay, Bonto, et al. "Current status of Rift Valley fever vaccine development." Vaccines 5.3 (2017): 29.
  2. Atkins, Colm, and Alexander N. Freiberg. "Recent advances in the development of antiviral therapeutics for Rift Valley fever virus infection." Future virology 12.11 (2017): 651-665.

All of our services and products are intended for preclinical research use only and cannot be used to diagnose, treat or manage patients.