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Characterization of Hemagglutinin Antigens on Influenza Virus and within Vaccines Using Electron Microscopy

Influenza viruses affect millions of people worldwide on an annual basis. Although vaccines are available, influenza still causes significant human mortality and morbidity. Vaccines target the major influenza surface glycoprotein hemagglutinin (HA). However, circulating HA subtypes undergo continual...

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Autores principales: Gallagher, John R., McCraw, Dustin M., Torian, Udana, Gulati, Neetu M., Myers, Mallory L., Conlon, Michael T., Harris, Audray K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6027289/
https://www.ncbi.nlm.nih.gov/pubmed/29799445
http://dx.doi.org/10.3390/vaccines6020031
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author Gallagher, John R.
McCraw, Dustin M.
Torian, Udana
Gulati, Neetu M.
Myers, Mallory L.
Conlon, Michael T.
Harris, Audray K.
author_facet Gallagher, John R.
McCraw, Dustin M.
Torian, Udana
Gulati, Neetu M.
Myers, Mallory L.
Conlon, Michael T.
Harris, Audray K.
author_sort Gallagher, John R.
collection PubMed
description Influenza viruses affect millions of people worldwide on an annual basis. Although vaccines are available, influenza still causes significant human mortality and morbidity. Vaccines target the major influenza surface glycoprotein hemagglutinin (HA). However, circulating HA subtypes undergo continual variation in their dominant epitopes, requiring vaccines to be updated annually. A goal of next-generation influenza vaccine research is to produce broader protective immunity against the different types, subtypes, and strains of influenza viruses. One emerging strategy is to focus the immune response away from variable epitopes, and instead target the conserved stem region of HA. To increase the display and immunogenicity of the HA stem, nanoparticles are being developed to display epitopes in a controlled spatial arrangement to improve immunogenicity and elicit protective immune responses. Engineering of these nanoparticles requires structure-guided design to optimize the fidelity and valency of antigen presentation. Here, we review electron microscopy applied to study the 3D structures of influenza viruses and different vaccine antigens. Structure-guided information from electron microscopy should be integrated into pipelines for the development of both more efficacious seasonal and universal influenza vaccine antigens. The lessons learned from influenza vaccine electron microscopic research could aid in the development of novel vaccines for other pathogens.
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spelling pubmed-60272892018-07-13 Characterization of Hemagglutinin Antigens on Influenza Virus and within Vaccines Using Electron Microscopy Gallagher, John R. McCraw, Dustin M. Torian, Udana Gulati, Neetu M. Myers, Mallory L. Conlon, Michael T. Harris, Audray K. Vaccines (Basel) Review Influenza viruses affect millions of people worldwide on an annual basis. Although vaccines are available, influenza still causes significant human mortality and morbidity. Vaccines target the major influenza surface glycoprotein hemagglutinin (HA). However, circulating HA subtypes undergo continual variation in their dominant epitopes, requiring vaccines to be updated annually. A goal of next-generation influenza vaccine research is to produce broader protective immunity against the different types, subtypes, and strains of influenza viruses. One emerging strategy is to focus the immune response away from variable epitopes, and instead target the conserved stem region of HA. To increase the display and immunogenicity of the HA stem, nanoparticles are being developed to display epitopes in a controlled spatial arrangement to improve immunogenicity and elicit protective immune responses. Engineering of these nanoparticles requires structure-guided design to optimize the fidelity and valency of antigen presentation. Here, we review electron microscopy applied to study the 3D structures of influenza viruses and different vaccine antigens. Structure-guided information from electron microscopy should be integrated into pipelines for the development of both more efficacious seasonal and universal influenza vaccine antigens. The lessons learned from influenza vaccine electron microscopic research could aid in the development of novel vaccines for other pathogens. MDPI 2018-05-25 /pmc/articles/PMC6027289/ /pubmed/29799445 http://dx.doi.org/10.3390/vaccines6020031 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Gallagher, John R.
McCraw, Dustin M.
Torian, Udana
Gulati, Neetu M.
Myers, Mallory L.
Conlon, Michael T.
Harris, Audray K.
Characterization of Hemagglutinin Antigens on Influenza Virus and within Vaccines Using Electron Microscopy
title Characterization of Hemagglutinin Antigens on Influenza Virus and within Vaccines Using Electron Microscopy
title_full Characterization of Hemagglutinin Antigens on Influenza Virus and within Vaccines Using Electron Microscopy
title_fullStr Characterization of Hemagglutinin Antigens on Influenza Virus and within Vaccines Using Electron Microscopy
title_full_unstemmed Characterization of Hemagglutinin Antigens on Influenza Virus and within Vaccines Using Electron Microscopy
title_short Characterization of Hemagglutinin Antigens on Influenza Virus and within Vaccines Using Electron Microscopy
title_sort characterization of hemagglutinin antigens on influenza virus and within vaccines using electron microscopy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6027289/
https://www.ncbi.nlm.nih.gov/pubmed/29799445
http://dx.doi.org/10.3390/vaccines6020031
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