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Influenza A (N1-N9) and Influenza B (B/Victoria and B/Yamagata) Neuraminidase Pseudotypes as Tools for Pandemic Preparedness and Improved Influenza Vaccine Design

To better understand how inhibition of the influenza neuraminidase (NA) protein contributes to protection against influenza, we produced lentiviral vectors pseudotyped with an avian H11 hemagglutinin (HA) and the NA of all influenza A (N1–N9) subtypes and influenza B (B/Victoria and B/Yamagata). The...

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Autores principales: da Costa, Kelly A. S., Del Rosario, Joanne Marie M., Ferrari, Matteo, Vishwanath, Sneha, Asbach, Benedikt, Kinsley, Rebecca, Wagner, Ralf, Heeney, Jonathan L., Carnell, George W., Temperton, Nigel J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9571397/
https://www.ncbi.nlm.nih.gov/pubmed/36146598
http://dx.doi.org/10.3390/vaccines10091520
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author da Costa, Kelly A. S.
Del Rosario, Joanne Marie M.
Ferrari, Matteo
Vishwanath, Sneha
Asbach, Benedikt
Kinsley, Rebecca
Wagner, Ralf
Heeney, Jonathan L.
Carnell, George W.
Temperton, Nigel J.
author_facet da Costa, Kelly A. S.
Del Rosario, Joanne Marie M.
Ferrari, Matteo
Vishwanath, Sneha
Asbach, Benedikt
Kinsley, Rebecca
Wagner, Ralf
Heeney, Jonathan L.
Carnell, George W.
Temperton, Nigel J.
author_sort da Costa, Kelly A. S.
collection PubMed
description To better understand how inhibition of the influenza neuraminidase (NA) protein contributes to protection against influenza, we produced lentiviral vectors pseudotyped with an avian H11 hemagglutinin (HA) and the NA of all influenza A (N1–N9) subtypes and influenza B (B/Victoria and B/Yamagata). These NA viral pseudotypes (PV) possess stable NA activity and can be utilized as target antigens in in vitro assays to assess vaccine immunogenicity. Employing these NA PV, we developed an enzyme-linked lectin assay (pELLA) for routine serology to measure neuraminidase inhibition (NI) titers of reference antisera, monoclonal antibodies and post-vaccination sera with various influenza antigens. We also show that the pELLA is more sensitive than the commercially available NA-Fluor™ in detecting NA inhibition in these samples. Our studies may lead to establishing the protective NA titer that contributes to NA-based immunity. This will aid in the design of superior, longer lasting and more broadly protective vaccines that can be employed together with HA-targeted vaccines in a pre-pandemic approach.
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spelling pubmed-95713972022-10-17 Influenza A (N1-N9) and Influenza B (B/Victoria and B/Yamagata) Neuraminidase Pseudotypes as Tools for Pandemic Preparedness and Improved Influenza Vaccine Design da Costa, Kelly A. S. Del Rosario, Joanne Marie M. Ferrari, Matteo Vishwanath, Sneha Asbach, Benedikt Kinsley, Rebecca Wagner, Ralf Heeney, Jonathan L. Carnell, George W. Temperton, Nigel J. Vaccines (Basel) Article To better understand how inhibition of the influenza neuraminidase (NA) protein contributes to protection against influenza, we produced lentiviral vectors pseudotyped with an avian H11 hemagglutinin (HA) and the NA of all influenza A (N1–N9) subtypes and influenza B (B/Victoria and B/Yamagata). These NA viral pseudotypes (PV) possess stable NA activity and can be utilized as target antigens in in vitro assays to assess vaccine immunogenicity. Employing these NA PV, we developed an enzyme-linked lectin assay (pELLA) for routine serology to measure neuraminidase inhibition (NI) titers of reference antisera, monoclonal antibodies and post-vaccination sera with various influenza antigens. We also show that the pELLA is more sensitive than the commercially available NA-Fluor™ in detecting NA inhibition in these samples. Our studies may lead to establishing the protective NA titer that contributes to NA-based immunity. This will aid in the design of superior, longer lasting and more broadly protective vaccines that can be employed together with HA-targeted vaccines in a pre-pandemic approach. MDPI 2022-09-14 /pmc/articles/PMC9571397/ /pubmed/36146598 http://dx.doi.org/10.3390/vaccines10091520 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
da Costa, Kelly A. S.
Del Rosario, Joanne Marie M.
Ferrari, Matteo
Vishwanath, Sneha
Asbach, Benedikt
Kinsley, Rebecca
Wagner, Ralf
Heeney, Jonathan L.
Carnell, George W.
Temperton, Nigel J.
Influenza A (N1-N9) and Influenza B (B/Victoria and B/Yamagata) Neuraminidase Pseudotypes as Tools for Pandemic Preparedness and Improved Influenza Vaccine Design
title Influenza A (N1-N9) and Influenza B (B/Victoria and B/Yamagata) Neuraminidase Pseudotypes as Tools for Pandemic Preparedness and Improved Influenza Vaccine Design
title_full Influenza A (N1-N9) and Influenza B (B/Victoria and B/Yamagata) Neuraminidase Pseudotypes as Tools for Pandemic Preparedness and Improved Influenza Vaccine Design
title_fullStr Influenza A (N1-N9) and Influenza B (B/Victoria and B/Yamagata) Neuraminidase Pseudotypes as Tools for Pandemic Preparedness and Improved Influenza Vaccine Design
title_full_unstemmed Influenza A (N1-N9) and Influenza B (B/Victoria and B/Yamagata) Neuraminidase Pseudotypes as Tools for Pandemic Preparedness and Improved Influenza Vaccine Design
title_short Influenza A (N1-N9) and Influenza B (B/Victoria and B/Yamagata) Neuraminidase Pseudotypes as Tools for Pandemic Preparedness and Improved Influenza Vaccine Design
title_sort influenza a (n1-n9) and influenza b (b/victoria and b/yamagata) neuraminidase pseudotypes as tools for pandemic preparedness and improved influenza vaccine design
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9571397/
https://www.ncbi.nlm.nih.gov/pubmed/36146598
http://dx.doi.org/10.3390/vaccines10091520
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