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Influenza Anti-Stalk Antibodies: Development of a New Method for the Evaluation of the Immune Responses to Universal Vaccine

Growing interest in universal influenza vaccines and novel administration routes has led to the development of alternative serological assays that are able to detect antibodies against conserved epitopes. We present a competitive ELISA method that is able to accurately determine the ratio of serum i...

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Autores principales: Manenti, Alessandro, Maciola, Agnieszka Katarzyna, Trombetta, Claudia Maria, Kistner, Otfried, Casa, Elisa, Hyseni, Inesa, Razzano, Ilaria, Torelli, Alessandro, Montomoli, Emanuele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7158664/
https://www.ncbi.nlm.nih.gov/pubmed/31991681
http://dx.doi.org/10.3390/vaccines8010043
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author Manenti, Alessandro
Maciola, Agnieszka Katarzyna
Trombetta, Claudia Maria
Kistner, Otfried
Casa, Elisa
Hyseni, Inesa
Razzano, Ilaria
Torelli, Alessandro
Montomoli, Emanuele
author_facet Manenti, Alessandro
Maciola, Agnieszka Katarzyna
Trombetta, Claudia Maria
Kistner, Otfried
Casa, Elisa
Hyseni, Inesa
Razzano, Ilaria
Torelli, Alessandro
Montomoli, Emanuele
author_sort Manenti, Alessandro
collection PubMed
description Growing interest in universal influenza vaccines and novel administration routes has led to the development of alternative serological assays that are able to detect antibodies against conserved epitopes. We present a competitive ELISA method that is able to accurately determine the ratio of serum immunoglobulin G directed against the different domains of the hemagglutinin, the head and the stalk. Human serum samples were treated with two variants of the hemagglutinin protein from the A/California/7/2009 influenza virus. The signals detected were assigned to different groups of antibodies and presented as a ratio between head and stalk domains. A subset of selected sera was also tested by hemagglutination inhibition, single radial hemolysis, microneutralization, and enzyme-linked lectin assays. Pre-vaccination samples from adults showed a quite high presence of anti-stalk antibodies, and the results were substantially in line with those of the classical serological assays. By contrast, pre-vaccination samples from children did not present anti-stalk antibodies, and the majority of the anti-hemagglutinin antibodies that were detected after vaccination were directed against the head domain. The presented approach, when supported by further assays, can be used to assess the presence of specific anti-stalk antibodies and the potential boost of broadly protective antibodies, especially in the case of novel universal influenza vaccine approaches.
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spelling pubmed-71586642020-04-21 Influenza Anti-Stalk Antibodies: Development of a New Method for the Evaluation of the Immune Responses to Universal Vaccine Manenti, Alessandro Maciola, Agnieszka Katarzyna Trombetta, Claudia Maria Kistner, Otfried Casa, Elisa Hyseni, Inesa Razzano, Ilaria Torelli, Alessandro Montomoli, Emanuele Vaccines (Basel) Article Growing interest in universal influenza vaccines and novel administration routes has led to the development of alternative serological assays that are able to detect antibodies against conserved epitopes. We present a competitive ELISA method that is able to accurately determine the ratio of serum immunoglobulin G directed against the different domains of the hemagglutinin, the head and the stalk. Human serum samples were treated with two variants of the hemagglutinin protein from the A/California/7/2009 influenza virus. The signals detected were assigned to different groups of antibodies and presented as a ratio between head and stalk domains. A subset of selected sera was also tested by hemagglutination inhibition, single radial hemolysis, microneutralization, and enzyme-linked lectin assays. Pre-vaccination samples from adults showed a quite high presence of anti-stalk antibodies, and the results were substantially in line with those of the classical serological assays. By contrast, pre-vaccination samples from children did not present anti-stalk antibodies, and the majority of the anti-hemagglutinin antibodies that were detected after vaccination were directed against the head domain. The presented approach, when supported by further assays, can be used to assess the presence of specific anti-stalk antibodies and the potential boost of broadly protective antibodies, especially in the case of novel universal influenza vaccine approaches. MDPI 2020-01-24 /pmc/articles/PMC7158664/ /pubmed/31991681 http://dx.doi.org/10.3390/vaccines8010043 Text en © 2020 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 Article
Manenti, Alessandro
Maciola, Agnieszka Katarzyna
Trombetta, Claudia Maria
Kistner, Otfried
Casa, Elisa
Hyseni, Inesa
Razzano, Ilaria
Torelli, Alessandro
Montomoli, Emanuele
Influenza Anti-Stalk Antibodies: Development of a New Method for the Evaluation of the Immune Responses to Universal Vaccine
title Influenza Anti-Stalk Antibodies: Development of a New Method for the Evaluation of the Immune Responses to Universal Vaccine
title_full Influenza Anti-Stalk Antibodies: Development of a New Method for the Evaluation of the Immune Responses to Universal Vaccine
title_fullStr Influenza Anti-Stalk Antibodies: Development of a New Method for the Evaluation of the Immune Responses to Universal Vaccine
title_full_unstemmed Influenza Anti-Stalk Antibodies: Development of a New Method for the Evaluation of the Immune Responses to Universal Vaccine
title_short Influenza Anti-Stalk Antibodies: Development of a New Method for the Evaluation of the Immune Responses to Universal Vaccine
title_sort influenza anti-stalk antibodies: development of a new method for the evaluation of the immune responses to universal vaccine
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7158664/
https://www.ncbi.nlm.nih.gov/pubmed/31991681
http://dx.doi.org/10.3390/vaccines8010043
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