Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10969153 | Vaccine | 2011 | 9 Pages |
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 8 h 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.
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Authors
Lisa D. Schlehuber, 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,