- Mucosis B.V.
- L.J. Zielstraweg 1
- 9713 GX Groningen
- Thomas Johnston
- +1 (240) 7535464
Mucosis Announces Publication of Preclinical Data Demonstrating Superior Protection by Mucosally Administered Mimopath®-Based Influenza Vaccines
Mimopath-based influenza vaccine protects against both homologous and heterologous challenge
According to the report, FluGEM®, a vaccine based on traditional inactivated influenza antigens formulated with bacterium-like particles (BLPs), provided full protection in mice against both homologous and heterologous influenza infection. Moreover, the results show more than 300-fold lower viral titers in the lungs when compared to conventional influenza vaccination. Reduction of viral lung titers more efficiently protects against disease, but may also result in decreased viral shedding, thereby increasing herd immunity. The data demonstrate that Mucosis' unique Mimopath® technology can be used to develop needle-free vaccines that are more efficacious than conventional vaccines.
Dr. Kees Leenhouts, CSO of Mucosis: "We are extremely pleased with the results of this study. It is a pivotal step in the further validation of our platform technology for the development of novel and improved vaccines to protect against infectious diseases."
Mucosis will continue to develop the FluGEM® vaccine candidate in cooperation with corporate, governmental and non-governmental partners. The company's lead vaccine candidate based on the same Mimopath® technology, called SynGEM(TM) , is designed to prevent infections with Respiratory Syncytial Virus (RSV), which affect over 60 million people worldwide ranging from the very young to the elderly with more than one million hospitalizations annually. An RSV vaccine does not yet exist.
About Mimopath® technology
The Mimopath® technology is based on Lactococcus lactis, a safe bacterium commonly used in the food industry. Mucosis has developed a robust technique to formulate the L. lactis bacteria into non-living bacterium-like particles (BLPs) that can be loaded with antigens from viral, bacterial, parasitic or tumor origin. The antigen-covered BLPs form a vaccine that can be delivered into the nose or mouth, without the need for a needle. These vaccines raise protective immunity by activation of both the innate and the adaptive immune system.
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