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Principles underlying rational design of live attenuated influenza vaccines

tetano

Editor, Senior Moderator
Clin Exp Vaccine Res. 2012 Jul;1(1):35-49. doi: 10.7774/cevr.2012.1.1.35. Epub 2012 Jul 31.
Principles underlying rational design of live attenuated influenza vaccines.
Jang YH, Seong BL.
Source

Laboratory of Molecular Medicine, Department of Biotechnology, College of Life Science and Biotechnology, Yonsei University, Seoul, Korea.
Abstract

Despite recent innovative advances in molecular virology and the developments of vaccines, influenza virus remains a serious burden for human health. Vaccination has been considered a primary countermeasure for prevention of influenza infection. Live attenuated influenza vaccines (LAIVs) are particularly attracting attention as an effective strategy due to several advantages over inactivated vaccines. Cold-adaptation, as a classical means for attenuating viral virulence, has been successfully used for generating safe and effective donor strains of LAIVs against seasonal epidemics and occasional pandemics. Recently, the advent of reverse genetics technique expedited a variety of rational strategies to broaden the pool of LAIVs. Considering the breadth of antigenic diversity of influenza virus, the pool of LAIVs is likely to equip us with better options for controlling influenza pandemics. With a brief reflection on classical attenuating strategies used at the initial stage of development of LAIVs, especially on the principles underlying the development of cold-adapted LAIVs, we further discuss and outline other attenuation strategies especially with respect to the rationales for attenuation, and their practicality for mass production. Finally, we propose important considerations for a rational vaccine design, which will provide us with practical guidelines for improving the safety and effectiveness of LAIVs.
KEYWORDS:

Attenuation strategy, Cold-adaptation, Cross protection, Influenza live attenuated vaccine

PMID:
23596576
[PubMed - in process]

http://www.ncbi.nlm.nih.gov/pubmed/23596576
 
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