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Vaccine technologies: From whole organisms to rationally designed protein assemblies
Vaccines have been the single most significant advancement in public health, preventing morbidity and mortality in millions of people annually. Vaccine development has traditionally focused on whole organism vaccines, either live attenuated or inactivated vaccines. While successful for many differen...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc.
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5079805/ https://www.ncbi.nlm.nih.gov/pubmed/27157411 http://dx.doi.org/10.1016/j.bcp.2016.05.001 |
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author | Karch, Christopher P. Burkhard, Peter |
author_facet | Karch, Christopher P. Burkhard, Peter |
author_sort | Karch, Christopher P. |
collection | PubMed |
description | Vaccines have been the single most significant advancement in public health, preventing morbidity and mortality in millions of people annually. Vaccine development has traditionally focused on whole organism vaccines, either live attenuated or inactivated vaccines. While successful for many different infectious diseases whole organisms are expensive to produce, require culture of the infectious agent, and have the potential to cause vaccine associated disease in hosts. With advancing technology and a desire to develop safe, cost effective vaccine candidates, the field began to focus on the development of recombinantly expressed antigens known as subunit vaccines. While more tolerable, subunit vaccines tend to be less immunogenic. Attempts have been made to increase immunogenicity with the addition of adjuvants, either immunostimulatory molecules or an antigen delivery system that increases immune responses to vaccines. An area of extreme interest has been the application of nanotechnology to vaccine development, which allows for antigens to be expressed on a particulate delivery system. One of the most exciting examples of nanovaccines are rationally designed protein nanoparticles. These nanoparticles use some of the basic tenants of structural biology, biophysical chemistry, and vaccinology to develop protective, safe, and easily manufactured vaccines. Rationally developed nanoparticle vaccines are one of the most promising candidates for the future of vaccine development. |
format | Online Article Text |
id | pubmed-5079805 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-50798052017-11-15 Vaccine technologies: From whole organisms to rationally designed protein assemblies Karch, Christopher P. Burkhard, Peter Biochem Pharmacol Research Update Vaccines have been the single most significant advancement in public health, preventing morbidity and mortality in millions of people annually. Vaccine development has traditionally focused on whole organism vaccines, either live attenuated or inactivated vaccines. While successful for many different infectious diseases whole organisms are expensive to produce, require culture of the infectious agent, and have the potential to cause vaccine associated disease in hosts. With advancing technology and a desire to develop safe, cost effective vaccine candidates, the field began to focus on the development of recombinantly expressed antigens known as subunit vaccines. While more tolerable, subunit vaccines tend to be less immunogenic. Attempts have been made to increase immunogenicity with the addition of adjuvants, either immunostimulatory molecules or an antigen delivery system that increases immune responses to vaccines. An area of extreme interest has been the application of nanotechnology to vaccine development, which allows for antigens to be expressed on a particulate delivery system. One of the most exciting examples of nanovaccines are rationally designed protein nanoparticles. These nanoparticles use some of the basic tenants of structural biology, biophysical chemistry, and vaccinology to develop protective, safe, and easily manufactured vaccines. Rationally developed nanoparticle vaccines are one of the most promising candidates for the future of vaccine development. Elsevier Inc. 2016-11-15 2016-05-06 /pmc/articles/PMC5079805/ /pubmed/27157411 http://dx.doi.org/10.1016/j.bcp.2016.05.001 Text en © 2016 Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Research Update Karch, Christopher P. Burkhard, Peter Vaccine technologies: From whole organisms to rationally designed protein assemblies |
title | Vaccine technologies: From whole organisms to rationally designed protein assemblies |
title_full | Vaccine technologies: From whole organisms to rationally designed protein assemblies |
title_fullStr | Vaccine technologies: From whole organisms to rationally designed protein assemblies |
title_full_unstemmed | Vaccine technologies: From whole organisms to rationally designed protein assemblies |
title_short | Vaccine technologies: From whole organisms to rationally designed protein assemblies |
title_sort | vaccine technologies: from whole organisms to rationally designed protein assemblies |
topic | Research Update |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5079805/ https://www.ncbi.nlm.nih.gov/pubmed/27157411 http://dx.doi.org/10.1016/j.bcp.2016.05.001 |
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