PROJECT SUMMARY The goal of this SBIR phase I proposal is to advance the development of a safe and efficacious virus-like particle (VLP) based-respiratory syncytial virus (RSV) vaccine to prevent the disease caused by this pathogen. The respiratory illnesses provoked by RSV in infants, children and the elderly are of global economical and public health impact. A recent worldwide estimate [1,2] indicates that over 33 million children under the age of five suffer RSV associated lower respiratory infections (ALRI) and at least 3 million are hospitalized and approximately 199,000 die of the disease each year. In the US, the CDC estimates that there are over 126,000 RSV associated pediatric hospitalizations at a cost of over $900 million per year. There is no vaccine currently licensed and treatments for the disease are limited; a prophylactic intervention relies on administering a neutralizing monoclonal antibody (Synagis®) to infants at risk of infection and to supportive care. A safe and effective vaccine would be the most desirable and cost effective preventive intervention. However, to date the creation of such a vaccine has not been attained and its development has been hindered by the enhancement of disease provoked by a formalin- inactivated RSV virus (FI-RSV) vaccine produced in the 1960’s. Other approaches have not proven successful and even dangerous. Here, we propose to further advance the development of a virus-like particle displaying RSV antigens as a strategy to create a safe and effective RSV vaccine. Our VLP approach displays two alternative conformation of the F protein, which is a novel and distinct strategy from other vaccine under development. Preliminary work on the immunogenicity, efficacy and safety of the RSVLP vaccine and summarized in the research strategy section showed that this vaccine is highly immunogenic and able to afford complete protection against virus challenge without the adverse reactions seen with a formalin inactivated RSV virus (FI-RSV) vaccine control [6]. VLPs are mimics of wild type virus particles but do not contain viral genetic material making them unable to replicate or cause infection. The particulate nature and redundant array of native antigen on the surface of the VLP incites a greater recognition by the immune system. We have successfully produced RSV-VLPs that display surface spikes of the F protein in its two different conformation, prefusion and postfusion. Vaccines formulated with these particles and tested in murine model of RSV demonstrated to be highly immunogenic, efficacious and safe [6]. In this application, we propose to continue the development of this vaccine performing additional preclinical testing in a second animal model, cotton rat, in order to select a candidate for further development toward clinical trials in humans. To fulfill these goals, we have designed three specific aims: Specific Aim 1- Months 1-4: Produce, purify and fully characterize RSVLP vaccine compositions conta...