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Modified vaccinia virus Ankara as antigen delivery system: how can we best use its potential?
Safety-tested modified vaccinia virus Ankara (MVA) has been established as a potent vector system for the development of candidate recombinant vaccines. The versatility of the vector system was recently demonstrated by the rapid production of experimental MVA vaccines for immunization against severe...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Ltd.
2004
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7127071/ https://www.ncbi.nlm.nih.gov/pubmed/15560976 http://dx.doi.org/10.1016/j.copbio.2004.09.001 |
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author | Drexler, Ingo Staib, Caroline Sutter, Gerd |
author_facet | Drexler, Ingo Staib, Caroline Sutter, Gerd |
author_sort | Drexler, Ingo |
collection | PubMed |
description | Safety-tested modified vaccinia virus Ankara (MVA) has been established as a potent vector system for the development of candidate recombinant vaccines. The versatility of the vector system was recently demonstrated by the rapid production of experimental MVA vaccines for immunization against severe acute respiratory syndrome associated coronavirus. Promising results were also obtained in the delivery of Epstein-Barr virus or human cytomegalovirus antigens and from the clinical testing of MVA vectors for vaccination against immunodeficiency virus, papilloma virus, Plasmodium falciparum or melanoma. Moreover, MVA is considered to be a prime candidate vaccine for safer protection against orthopoxvirus infections. Thus, vector development to challenge dilemmas in vaccinology or immunization against poxvirus biothreat seems possible, yet the right choice should be made for a most beneficial use. |
format | Online Article Text |
id | pubmed-7127071 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | Elsevier Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-71270712020-04-08 Modified vaccinia virus Ankara as antigen delivery system: how can we best use its potential? Drexler, Ingo Staib, Caroline Sutter, Gerd Curr Opin Biotechnol Article Safety-tested modified vaccinia virus Ankara (MVA) has been established as a potent vector system for the development of candidate recombinant vaccines. The versatility of the vector system was recently demonstrated by the rapid production of experimental MVA vaccines for immunization against severe acute respiratory syndrome associated coronavirus. Promising results were also obtained in the delivery of Epstein-Barr virus or human cytomegalovirus antigens and from the clinical testing of MVA vectors for vaccination against immunodeficiency virus, papilloma virus, Plasmodium falciparum or melanoma. Moreover, MVA is considered to be a prime candidate vaccine for safer protection against orthopoxvirus infections. Thus, vector development to challenge dilemmas in vaccinology or immunization against poxvirus biothreat seems possible, yet the right choice should be made for a most beneficial use. Elsevier Ltd. 2004-12 2004-10-13 /pmc/articles/PMC7127071/ /pubmed/15560976 http://dx.doi.org/10.1016/j.copbio.2004.09.001 Text en Copyright © 2004 Elsevier Ltd. 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 | Article Drexler, Ingo Staib, Caroline Sutter, Gerd Modified vaccinia virus Ankara as antigen delivery system: how can we best use its potential? |
title | Modified vaccinia virus Ankara as antigen delivery system: how can we best use its potential? |
title_full | Modified vaccinia virus Ankara as antigen delivery system: how can we best use its potential? |
title_fullStr | Modified vaccinia virus Ankara as antigen delivery system: how can we best use its potential? |
title_full_unstemmed | Modified vaccinia virus Ankara as antigen delivery system: how can we best use its potential? |
title_short | Modified vaccinia virus Ankara as antigen delivery system: how can we best use its potential? |
title_sort | modified vaccinia virus ankara as antigen delivery system: how can we best use its potential? |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7127071/ https://www.ncbi.nlm.nih.gov/pubmed/15560976 http://dx.doi.org/10.1016/j.copbio.2004.09.001 |
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