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A systems approach to designing next generation vaccines: combining α-galactose modified antigens with nanoparticle platforms

Innovative vaccine platforms are needed to develop effective countermeasures against emerging and re-emerging diseases. These platforms should direct antigen internalization by antigen presenting cells and promote immunogenic responses. This work describes an innovative systems approach combining tw...

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Autores principales: Phanse, Yashdeep, Carrillo-Conde, Brenda R., Ramer-Tait, Amanda E., Broderick, Scott, Kong, Chang Sun, Rajan, Krishna, Flick, Ramon, Mandell, Robert B., Narasimhan, Balaji, Wannemuehler, Michael J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3895907/
https://www.ncbi.nlm.nih.gov/pubmed/24441019
http://dx.doi.org/10.1038/srep03775
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author Phanse, Yashdeep
Carrillo-Conde, Brenda R.
Ramer-Tait, Amanda E.
Broderick, Scott
Kong, Chang Sun
Rajan, Krishna
Flick, Ramon
Mandell, Robert B.
Narasimhan, Balaji
Wannemuehler, Michael J.
author_facet Phanse, Yashdeep
Carrillo-Conde, Brenda R.
Ramer-Tait, Amanda E.
Broderick, Scott
Kong, Chang Sun
Rajan, Krishna
Flick, Ramon
Mandell, Robert B.
Narasimhan, Balaji
Wannemuehler, Michael J.
author_sort Phanse, Yashdeep
collection PubMed
description Innovative vaccine platforms are needed to develop effective countermeasures against emerging and re-emerging diseases. These platforms should direct antigen internalization by antigen presenting cells and promote immunogenic responses. This work describes an innovative systems approach combining two novel platforms, αGalactose (αGal)-modification of antigens and amphiphilic polyanhydride nanoparticles as vaccine delivery vehicles, to rationally design vaccine formulations. Regimens comprising soluble αGal-modified antigen and nanoparticle-encapsulated unmodified antigen induced a high titer, high avidity antibody response with broader epitope recognition of antigenic peptides than other regimen. Proliferation of antigen-specific CD4(+) T cells was also enhanced compared to a traditional adjuvant. Combining the technology platforms and augmenting immune response studies with peptide arrays and informatics analysis provides a new paradigm for rational, systems-based design of next generation vaccine platforms against emerging and re-emerging pathogens.
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spelling pubmed-38959072014-01-21 A systems approach to designing next generation vaccines: combining α-galactose modified antigens with nanoparticle platforms Phanse, Yashdeep Carrillo-Conde, Brenda R. Ramer-Tait, Amanda E. Broderick, Scott Kong, Chang Sun Rajan, Krishna Flick, Ramon Mandell, Robert B. Narasimhan, Balaji Wannemuehler, Michael J. Sci Rep Article Innovative vaccine platforms are needed to develop effective countermeasures against emerging and re-emerging diseases. These platforms should direct antigen internalization by antigen presenting cells and promote immunogenic responses. This work describes an innovative systems approach combining two novel platforms, αGalactose (αGal)-modification of antigens and amphiphilic polyanhydride nanoparticles as vaccine delivery vehicles, to rationally design vaccine formulations. Regimens comprising soluble αGal-modified antigen and nanoparticle-encapsulated unmodified antigen induced a high titer, high avidity antibody response with broader epitope recognition of antigenic peptides than other regimen. Proliferation of antigen-specific CD4(+) T cells was also enhanced compared to a traditional adjuvant. Combining the technology platforms and augmenting immune response studies with peptide arrays and informatics analysis provides a new paradigm for rational, systems-based design of next generation vaccine platforms against emerging and re-emerging pathogens. Nature Publishing Group 2014-01-20 /pmc/articles/PMC3895907/ /pubmed/24441019 http://dx.doi.org/10.1038/srep03775 Text en Copyright © 2014, Macmillan Publishers Limited. All rights reserved http://creativecommons.org/licenses/by-nc-nd/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/3.0/
spellingShingle Article
Phanse, Yashdeep
Carrillo-Conde, Brenda R.
Ramer-Tait, Amanda E.
Broderick, Scott
Kong, Chang Sun
Rajan, Krishna
Flick, Ramon
Mandell, Robert B.
Narasimhan, Balaji
Wannemuehler, Michael J.
A systems approach to designing next generation vaccines: combining α-galactose modified antigens with nanoparticle platforms
title A systems approach to designing next generation vaccines: combining α-galactose modified antigens with nanoparticle platforms
title_full A systems approach to designing next generation vaccines: combining α-galactose modified antigens with nanoparticle platforms
title_fullStr A systems approach to designing next generation vaccines: combining α-galactose modified antigens with nanoparticle platforms
title_full_unstemmed A systems approach to designing next generation vaccines: combining α-galactose modified antigens with nanoparticle platforms
title_short A systems approach to designing next generation vaccines: combining α-galactose modified antigens with nanoparticle platforms
title_sort systems approach to designing next generation vaccines: combining α-galactose modified antigens with nanoparticle platforms
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3895907/
https://www.ncbi.nlm.nih.gov/pubmed/24441019
http://dx.doi.org/10.1038/srep03775
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