Cerus Corporation Acknowledges Growing Monkeypox Outbreak and Public Health Emergency
Cerus Corporation (NASDAQ: CERS) acknowledges the U.S. Department of Health and Human Services' declaration of monkeypox as a national Public Health Emergency, with over 10,000 reported cases in the U.S. and 30,000 globally. The company highlights its INTERCEPT Blood System, which has been effective in inactivating a broad spectrum of pathogens, including the vaccinia virus, a close relative of monkeypox. This technology provides essential support in safeguarding the blood supply against emerging infectious diseases, ensuring blood safety and availability during outbreaks.
- INTERCEPT Blood System effectively inactivates pathogens, enhancing blood safety.
- Over 300 blood centers globally utilize INTERCEPT, reflecting its market acceptance.
- INTERCEPT technology provides proactive solutions to emerging infectious diseases.
- Monkeypox cases pose a risk, highlighting potential vulnerabilities in blood safety.
- No current evidence of monkeypox being transfusion-transmitted, but limited data exist.
Spread of monkeypox infections serves as another real-world example of the ongoing risk of emerging pathogens and the potential role for pathogen reduction technology, like the INTERCEPT Blood System, in securing the blood supply
While to date monkeypox has not been reported to be a transfusion-transmitted infectious disease (TTID), only limited data are available currently. For nearly two decades, the INTERCEPT Blood System for platelets and plasma has been shown to inactivate a broad spectrum of pathogens. In a previous study with INTERCEPT platelets, vaccinia virus, a member of the Poxiviridae family which includes smallpox and monkeypox, was inactivated to high levels.1
In recent years, pathogen inactivation technologies have played an important role in prospective risk reduction of transfusion associated emerging infectious diseases like West Nile Virus, Zika and Chikungunya. INTERCEPT can be implemented before tests for these infectious targets are developed and available. Blood transfusions are a common and critical supportive therapy used for many types of patients. Pathogen inactivation technologies, such as Cerus’ INTERCEPT Blood System for platelets and plasma, provide blood centers with a proactive solution to help secure blood safety and availability.
“The current monkeypox outbreak serves as yet another in a long list of reminders that the emergence of pathogens across the globe can have dangerous and disruptive impacts to blood donors, patients, and healthcare systems everywhere,” stated William ‘Obi’ Greenman, Cerus’ president and chief executive officer. “Looking at the historical challenges of managing risk and uncertainty in the blood supply, it is good to witness the peace of mind that the INTERCEPT Blood System affords our blood center and hospital customers now that many countries have implemented our technology for the majority of their platelet components.”
ABOUT THE INTERCEPT BLOOD SYSTEM
Over 300 blood centers globally use the INTERCEPT Blood System for platelets and/or plasma as a proactive approach designed to help protect the blood supply from a wide range of pathogens by inactivating contaminants from donated units. By providing broad spectrum protection to these blood components, pathogen reduction technology like the INTERCEPT Blood System can serve as a proactive safeguard for the blood supply, particularly in instances where testing does not currently exist for an emerging target, thus enabling continuous donor availability during an outbreak.
In nearly a dozen countries, INTERCEPT platelets are the standard of care for their respective national platelet supplies. No pathogen inactivation system has been shown to inactivate all pathogens. For more information on the INTERCEPT Blood System visit www.cerus.com.
ABOUT
INTERCEPT and the INTERCEPT Blood System are trademarks of
1 Lin L, et al. Inactivation of viruses in platelet concentrates by photochemical treatment with amotosalen and long-wavelength ultraviolet light. Transfusion 2005;45:580-590
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