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The cell-derived monovalent H1N1 swine-origin influenza vaccine, marketed under the brand name Celtura, is an inactivated, cell culture-derived, monovalent subunit influenza virus vaccine developed to prevent pandemic influenza caused by the swine-origin A/H1N1 virus. Developed by Novartis Vaccines and Diagnostics (with the influenza vaccine portfolio later acquired by Seqirus, a CSL company), the vaccine contains hemagglutinin (HA) and neuraminidase surface antigens derived from the A/California/7/2009 (H1N1)v-like strain (specifically the X-179A reassortant). Unlike traditional egg-based vaccines, Celtura is produced in Madin-Darby Canine Kidney (MDCK) cell culture, offering a faster and more scalable manufacturing process during a pandemic. It is formulated with the MF59 oil-in-water emulsion adjuvant to enhance immunogenicity and enable antigen dose sparing, allowing for a robust immune response even at low antigen doses (3.75 µg). The vaccine was approved in several European countries, including Germany and Switzerland, during the 2009 H1N1 influenza pandemic.
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