| Literature DB >> 21272601 |
Yasuko Hatta1, Masato Hatta, Pamuk Bilsel, Gabriele Neumann, Yoshihiro Kawaoka.
Abstract
The 2009 influenza pandemic brought home the importance of vaccines in infection control. Previously, we demonstrated an M2 cytoplasmic tail mutant H5N1 influenza virus could serve as a live-attenuated vaccine. Here, we adapted that strategy, generating a mutant pandemic (H1N1) 2009 virus that grew well in cell culture, but replicated less well in mice than did wild-type virus. The mutant virus elicited sterile immunity in mice, completely protecting them from challenge with a pandemic (H1N1) 2009 virus. Our results indicate that M2 cytoplasmic tail mutants are suitable for live-attenuated vaccines against pandemic viruses.Entities:
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Year: 2011 PMID: 21272601 PMCID: PMC3132197 DOI: 10.1016/j.vaccine.2011.01.023
Source DB: PubMed Journal: Vaccine ISSN: 0264-410X Impact factor: 3.641