Technology ID
TAB-2721

Respiratory Syncytial Virus Immunogens for Vaccine and Therapeutics Development

E-Numbers
E-197-2013-0
E-197-2013-2
Lead Inventor
Anderson, Larry (CDC)
Co-Inventors
Haynes, Lia (CDC)
Tripp, Ralph (University of Georgia)
Applications
Vaccines­­­
Therapeutics
Research Materials
Diagnostics
Consumer Products
Therapeutic Areas
Ophthalmology
Oncology
Infectious Disease
Immunology
Endocrinology
Dental
Cardiology
Development Stages
Pre-Clinical (in vitro)
Development Status
  • In vitro data available
  • In vivo data available (animal)
  • Research Products
    Research Equipment
    Antibodies
    Lead IC
    CDC
    ICs
    CDC
    CDC researchers have developed specific Respiratory Syncytial Virus (RSV) immunogens for use in the development of RSV-directed vaccines and therapeutics. RSV is the most common cause of serious respiratory disease in infants and young children and an important cause of disease in the elderly. To date, efforts to make a mutually safe and effective vaccine have been largely unsuccessful. This invention addresses both problems.

    CDC and collaborative researchers have demonstrated that a vaccine based on amino acid sequences corresponding to group-specific regions of the RSV G-protein can effectively induce antibodies, facilitate virus clearance, decrease the virus-induced inflammatory response to RSV challenge, and also decrease the enhanced disease following RSV challenge. This composition may be used alone as a vaccine to safely protect infants, children, and adults from RSV, as a booster with other RSV proteins or with inactivated virus as a vaccine to ensure that it can be given safely and effectively improve protection from RSV.

    Commercial Applications
    • Prophylactic and therapeutic for the prevention and treatment of RSV infections
    • Single or multi-component vaccine against RSV
    • Improvements to currently developed/developing vaccines
    • Developed antibodies may be employed for use in passive immunity or RSV research
    Competitive Advantages
    • Increased safety, effectiveness compared to current vaccines
    • Findings suggest likely prevention or mitigation of RSV-related pulmonary disease for previously established infections
    Licensing Contact:
    Motley, Jonathan
    jonathan.motley@nih.gov