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Kinetic of the Antibody Response Following AddaVax-Adjuvanted Immunization with Recombinant Influenza Antigens

Notwithstanding the current SARS-CoV-2 pandemic, influenza virus infection still represents a global health concern in terms of hospitalizations and possible pandemic threats. The objective of next-generation influenza vaccines is not only to increase the breadth of response but also to improve the...

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Autores principales: Ross, Ted. M., Gokanapudi, Naveen, Ge, Pan, Shi, Hua, Richardson, Robert A., Pierce, Spencer R., Sanchez, Pedro, Ullah, Subhan, De Luca, Eliana, Sautto, Giuseppe A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9415944/
https://www.ncbi.nlm.nih.gov/pubmed/36016202
http://dx.doi.org/10.3390/vaccines10081315
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author Ross, Ted. M.
Gokanapudi, Naveen
Ge, Pan
Shi, Hua
Richardson, Robert A.
Pierce, Spencer R.
Sanchez, Pedro
Ullah, Subhan
De Luca, Eliana
Sautto, Giuseppe A.
author_facet Ross, Ted. M.
Gokanapudi, Naveen
Ge, Pan
Shi, Hua
Richardson, Robert A.
Pierce, Spencer R.
Sanchez, Pedro
Ullah, Subhan
De Luca, Eliana
Sautto, Giuseppe A.
author_sort Ross, Ted. M.
collection PubMed
description Notwithstanding the current SARS-CoV-2 pandemic, influenza virus infection still represents a global health concern in terms of hospitalizations and possible pandemic threats. The objective of next-generation influenza vaccines is not only to increase the breadth of response but also to improve the elicitation of an effective and robust immune response, especially in high-risk populations. To achieve this second objective, the administration of adjuvanted influenza vaccines has been considered. In this regard, the monitoring and characterization of the antibody response associated with the administration of adjuvanted vaccines has been evaluated in this study in order to shed light on the kinetic, magnitude and subclass usage of antibody secreting cells (ASCs) as well as of circulating antigen-specific serum antibodies. Specifically, we utilized the DBA/2J mouse model to assess the kinetic, magnitude and IgG subclass usage of the antibody response following an intramuscular (IM) or intraperitoneal (IP) immunization regimen with AddaVax-adjuvanted bivalent H1N1 and H3N2 computationally optimized broadly reactive antigen (COBRA) influenza recombinant hemagglutinins (rHAs). While the serological evaluation revealed a homogeneous kinetic of the antibody response, the detection of the ASCs through a FluoroSpot platform revealed a different magnitude, subclass usage and kinetic of the antigen-specific IgG secreting cells peaking at day 5 and day 9 following the IP and IM immunization, respectively.
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spelling pubmed-94159442022-08-27 Kinetic of the Antibody Response Following AddaVax-Adjuvanted Immunization with Recombinant Influenza Antigens Ross, Ted. M. Gokanapudi, Naveen Ge, Pan Shi, Hua Richardson, Robert A. Pierce, Spencer R. Sanchez, Pedro Ullah, Subhan De Luca, Eliana Sautto, Giuseppe A. Vaccines (Basel) Communication Notwithstanding the current SARS-CoV-2 pandemic, influenza virus infection still represents a global health concern in terms of hospitalizations and possible pandemic threats. The objective of next-generation influenza vaccines is not only to increase the breadth of response but also to improve the elicitation of an effective and robust immune response, especially in high-risk populations. To achieve this second objective, the administration of adjuvanted influenza vaccines has been considered. In this regard, the monitoring and characterization of the antibody response associated with the administration of adjuvanted vaccines has been evaluated in this study in order to shed light on the kinetic, magnitude and subclass usage of antibody secreting cells (ASCs) as well as of circulating antigen-specific serum antibodies. Specifically, we utilized the DBA/2J mouse model to assess the kinetic, magnitude and IgG subclass usage of the antibody response following an intramuscular (IM) or intraperitoneal (IP) immunization regimen with AddaVax-adjuvanted bivalent H1N1 and H3N2 computationally optimized broadly reactive antigen (COBRA) influenza recombinant hemagglutinins (rHAs). While the serological evaluation revealed a homogeneous kinetic of the antibody response, the detection of the ASCs through a FluoroSpot platform revealed a different magnitude, subclass usage and kinetic of the antigen-specific IgG secreting cells peaking at day 5 and day 9 following the IP and IM immunization, respectively. MDPI 2022-08-14 /pmc/articles/PMC9415944/ /pubmed/36016202 http://dx.doi.org/10.3390/vaccines10081315 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 Communication
Ross, Ted. M.
Gokanapudi, Naveen
Ge, Pan
Shi, Hua
Richardson, Robert A.
Pierce, Spencer R.
Sanchez, Pedro
Ullah, Subhan
De Luca, Eliana
Sautto, Giuseppe A.
Kinetic of the Antibody Response Following AddaVax-Adjuvanted Immunization with Recombinant Influenza Antigens
title Kinetic of the Antibody Response Following AddaVax-Adjuvanted Immunization with Recombinant Influenza Antigens
title_full Kinetic of the Antibody Response Following AddaVax-Adjuvanted Immunization with Recombinant Influenza Antigens
title_fullStr Kinetic of the Antibody Response Following AddaVax-Adjuvanted Immunization with Recombinant Influenza Antigens
title_full_unstemmed Kinetic of the Antibody Response Following AddaVax-Adjuvanted Immunization with Recombinant Influenza Antigens
title_short Kinetic of the Antibody Response Following AddaVax-Adjuvanted Immunization with Recombinant Influenza Antigens
title_sort kinetic of the antibody response following addavax-adjuvanted immunization with recombinant influenza antigens
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9415944/
https://www.ncbi.nlm.nih.gov/pubmed/36016202
http://dx.doi.org/10.3390/vaccines10081315
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