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The Marburg virus disease is non-preventable, posing a serious and fatal illness to both humans and non-human primates. Our firm's dedication to developing forward looking solutions has helped us become a key player in combating Marburg virus disease and subsequently facilitates the creation of safe and effective vaccines and therapeutics.
Marburg virus disease (MVD) is a viral hemorrhagic fever of high morbidity caused by the Marburg virus (MARV) which belongs to the filovirus family, relatives of the Ebola virus. MVD was first described during two sets of concurrent outbreaks in Germany and Serbia in 1967. Since then, it has been MVD has been associated with numerous outbreaks in Africa. MVD has a case fatality rate of as high as 88%. It is a zoonotic disease, and fruit bats, particularly Rousettus aegyptiacus, are considered the primary reservoir. Humans acquire the virus through contact with infected animals or non-airborne infectious body fluids.
Fig.1 Pathophysiology of Marburg virus (MARV) infection. (Chakraborty S., et al., 2022)
Recombinant Vector Vaccines
The use of such Recombinant vector vaccines has shown efficiency in preclinical studies. Such vaccines are constructed using an inoffensive virus or a bacterium which carries a portion of the MARV genome allowing the infected host cells to mount an immune response without causing the disease process. For instance, the rVSV vaccine has exhibited total protective measures when administered postexposure in non-human primate models.
DNA and RNA Vaccines
Asynchronous vaccine approaches such as DNA or RNA vaccines are new in the sense that the genetic material coding for the MARV antigens is placed right in the host cells. Such a technology makes these vaccines easier to develop and enables broader immune responses. As an example, the Marburg glycoprotein DNA vaccine has been developed and clinical trials for safety and immunogenicity tests are in progress.
Virus-Like Particle (VLP) Vaccines
VLP Vaccines are Virus Like Particles Vaccines that activate an immune response while using only fragments of the intact viral structure. There has been research on the development of VLPs aimed at the Marburg virus (MARV) and it has focused on the glycoprotein on the surface of the virus that is crucial for binding to and penetrating the host cells. These virus-like particles have been immunized and are tested for the effectiveness in production of neutralizing antibodies at the tested preclinical stages.
We offer a comprehensive set of services ranging from the development of MVD vaccines and therapeutics to their advancements. We focus on:
Our preclinical research services are designed to provide robust data supporting vaccine and therapeutic development. We utilize state-of-the-art facilities and techniques to conduct comprehensive studies. If you are interested in our services, please feel free to contact us.
References
All of our services and products are intended for preclinical research use only and cannot be used to diagnose, treat or manage patients.