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Defining the antibody cross-reactome against the influenza virus surface glycoproteins

Influenza virus infections induce antibodies against the viral surface glycoproteins hemagglutinin and neuraminidase, and these responses can be broadly protective. To test the breadth and magnitude of antibody responses, mice, guinea pigs and ferrets were sequentially infected with divergent H1N1 o...

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Detalles Bibliográficos
Autores principales: Nachbagauer, Raffael, Choi, Angela, Hirsh, Ariana, Margine, Irina, Iida, Sayaka, Barrera, Aldo, Ferres, Marcela, Albrecht, Randy A., García-Sastre, Adolfo, Bouvier, Nicole M., Ito, Kimihito, Medina, Rafael A., Palese, Peter, Krammer, Florian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5360498/
https://www.ncbi.nlm.nih.gov/pubmed/28192418
http://dx.doi.org/10.1038/ni.3684
Descripción
Sumario:Influenza virus infections induce antibodies against the viral surface glycoproteins hemagglutinin and neuraminidase, and these responses can be broadly protective. To test the breadth and magnitude of antibody responses, mice, guinea pigs and ferrets were sequentially infected with divergent H1N1 or H3N2 viruses. Antibody responses were measured by ELISA against an extensive panel of recombinant glycoproteins representing the viral diversity in nature. Guinea pigs developed high titers of broadly cross-reactive antibodies; mice and ferrets exhibited narrower humoral responses. Then, we compared antibody responses after H1N1 or H3N2 infections in humans and found markedly broad responses and cogent evidence for original antigenic sin. This work will inform universal influenza vaccine design and can guide pandemic preparedness efforts against emerging influenza viruses.