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Genetic engineering of live attenuated influenza viruses

tetano

Editor, Senior Moderator
Methods Mol Biol. 2012;865:163-74.
Genetic engineering of live attenuated influenza viruses.
Jin H, Chen Z, Liu J, Kemble G.
Source

MedImmune, Mountain View, CA, USA, jinh@medimmune.com.
Abstract

The first live attenuated influenza vaccine (LAIV) was licensed in the USA in 2003; it is a trivalent vaccine composed of two type A (H1N1 and H3N2) and one type B influenza virus each at 10(7) fluorescent focus units (FFU). Each influenza vaccine strain is a reassortant virus that contains the hemagglutinin (HA) and neuraminidase (NA) gene segments from a wild-type influenza virus and the six internal protein gene segments from a master donor virus (MDV) of either cold-adapted A/Ann Arbor/6/60 or B/Ann Arbor/1/66. MDV confers the cold-adapted, temperature-sensitive, and attenuation phenotypes to the vaccine strains. The reassortant vaccine seeds are currently produced by reverse genetics and amplified in specific pathogen-free (SPF) 9-11 days old embryonated chicken eggs for manufacture. In addition, MDCK cell culture manufacture processes have been developed to produce LAIV for research use and with modifications for clinical and/or commercial grade material production.

PMID:
22528159
[PubMed - in process]

http://www.ncbi.nlm.nih.gov/pubmed/22528159
 
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