In summary, PIV5 is safe, stable, efficacious, cost–effective to produce, and overcomes pre-existing anti-vector immunity. In this work, we have shown that PIV5-based RSV vaccine candidates have the potential to be effective RSV vaccines, providing an additional option for RSV vaccine development. We appreciate the helpful discussion and technical assistance from all members of Biao He’s laboratory. This work was partially supported by grants from the National Institute of Allergy and Infectious Diseases (R01AI070847) to B.H. and (R01AI081977) to M.N.T. “
“The novel H1N1 influenza virus was detected in the United

States in April 2009. Worldwide, a pandemic was declared, and a national public health emergency was announced in the United States. In the US, plans were made for High Content Screening a national vaccination campaign to be rolled out in Fall 2009, when the pandemic H1N1 vaccine would be available. The campaign was implemented as a public–private partnership, with federal purchase of the vaccine. The Centers for Disease Control

and Prevention (CDC) allocated vaccine pro rata to states by total population as the vaccine became available. States determined how vaccine would be allocated in their jurisdiction and either retained Selleckchem EPZ-6438 control of vaccine allocation to individual providers at the central level or delegated fully or partially to local jurisdictions. States or local jurisdictions invited providers to participate in the program and vaccine was shipped to designated providers through a centralized distribution process supervised by the CDC that built on an existing contract for

Digestive enzyme management and distribution of vaccines in the Vaccine for Children (VFC) program. Fig. 1 shows a basic scheme of the supply chain for H1N1 vaccine from manufacturer to provider. State decisions about where to direct vaccine were guided by recommendations of the CDC’s Advisory Committee on Immunization Practices (ACIP) [6], which recommended that the vaccine be initially directed to: pregnant women, persons who live with or provide care for infants aged <6 months, health-care and emergency medical services personnel who have direct contact with patients or infectious material, all people 6 months to 24 years of age, and persons aged 25 through 64 years with certain health conditions (“high-risk”). The recommendations also provided further specification of priority groups in the event of vaccine shortage and stated that decisions to broaden availability of vaccine should be made at the local level. Overall, more than 120 million doses of vaccine were distributed to over 70 thousand locations by April 2010 [4], [8] and [9] and 80.8 million people reported having been vaccinated [10]. The vaccine supply was insufficient to meet demand initially, and became more plentiful after Thanksgiving, a time when demand for influenza vaccination traditionally slows.