| Literature DB >> 21616113 |
Lisa D Schlehuber1, Iain J McFadyen, Yu Shu, James Carignan, W Paul Duprex, William R Forsyth, Jason H Ho, Christine M Kitsos, George Y Lee, Douglas A Levinson, Sarah C Lucier, Christopher B Moore, Niem T Nguyen, Josephine Ramos, B André Weinstock, Junhong Zhang, Julie A Monagle, Colin R Gardner, Juan C Alvarez.
Abstract
As a result of thermal instability, some live attenuated viral (LAV) vaccines lose substantial potency from the time of manufacture to the point of administration. Developing regions lacking extensive, reliable refrigeration ("cold-chain") infrastructure are particularly vulnerable to vaccine failure, which in turn increases the burden of disease. Development of a robust, infectivity-based high throughput screening process for identifying thermostable vaccine formulations offers significant promise for vaccine development across a wide variety of LAV products. Here we describe a system that incorporates thermal stability screening into formulation design using heat labile measles virus as a prototype. The screening of >11,000 unique formulations resulted in the identification of liquid formulations with marked improvement over those used in commercial monovalent measles vaccines, with <1.0 log loss of activity after incubation for 8h at 40°C. The approach was shown to be transferable to a second unrelated virus, and therefore offers significant promise towards the optimization of formulation for LAV vaccine products.Entities:
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Year: 2011 PMID: 21616113 DOI: 10.1016/j.vaccine.2011.04.079
Source DB: PubMed Journal: Vaccine ISSN: 0264-410X Impact factor: 3.641