DK and OT are employees of HealthCore, Inc. SB has received a single honorarium from MedImmune for the development of an educational presentation. Contributors: Study concept and design: EA and CA Acquisition of data: DK, OT, and EA. Analysis and interpretation of data: all authors. Drafting of the manuscript and critical revision of the manuscript for important intellectual content: EA, DK, and CA and critical review and editing of the manuscript: all authors. Statistical analysis: DK and EA. All authors approved the final manuscript for submission.

Financial disclosures: EA was an employee of MedImmune, Gaithersburg, MD when the study was conducted and manuscript written. CA and HC are employees of AstraZeneca, the parent company Selleck NU7441 of MedImmune, Gaithersburg, MD and may have stock or stock options. DK and OT are employees of HealthCore, Inc. SB has received a single honorarium from MedImmune for the development of an educational presentation. Funding support: This research was funded by MedImmune. Role of the sponsor: Drs. Ambrose, and Caspard are employees

of AstraZeneca, the parent company of MedImmune. MedImmune funded the study, therefore, the role of the sponsor included study design, collection, analysis, and interpretation of data, writing the report, and the decision to submit the article for publication. Additional contributions: Editorial assistance was provided by Susan E. HDAC inhibitor DeRocco, PhD, and John E. Fincke, PhD, of Complete Healthcare Communications, Inc. (Chadds Ford, PA) and funded by MedImmune. “
“Vaccination is the cornerstone of the global public health strategy to mitigate an eventual influenza pandemic. Rapid production of vaccine to immunize billions of people in a short period of time requires development Cell press of alternative manufacturing platforms, such as large-scale animal cell culture bioreactors. In combination with other methods, cell-based manufacturing would augment vaccine manufacturing capacity to respond to a pandemic [1]. MDCK and VERO cell culture–derived influenza vaccines have

received regulatory approval in some countries [2] and [3]. Influenza vaccines produced in cell cultures have relied on candidate vaccine viruses developed by the WHO GISRS laboratories for vaccine production in embryonated eggs [4]. Although these viruses are ideal for the traditional method of vaccine production in eggs, the growth can be suboptimal for production of vaccines in cell cultures [4]. A sustainable supply of circulating influenza viruses isolated in cell cultures that meet regulatory requirements would be required to support cell-based vaccine manufacturing. Critical information on the comparative performance of several regulatory requirement-compliant cell lines for isolation of influenza viruses from clinical species for subsequent use as candidate vaccine viruses is not available.