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707 post-2009 A(H1N1)pdm09 NA sequences were analyzed computationally to design two mRNA vaccine constructs. Mice immunized with NA-D1 or NA-E2 constructs were challenged with homologous H1N1 or heterologous H5N1 viruses. The data likely contains results on antibody titers and protection efficacy, supporting NA as a complementary antigen for broader influenza vaccines.
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