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Viral vectors for malaria vaccine development

A workshop on viral vectors for malaria vaccine development, organized by the PATH Malaria Vaccine Initiative, was held in Bethesda, MD on October 20, 2005. Recent advancements in viral-vectored malaria vaccine development and emerging vector technologies were presented and discussed. Classic viral...

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Autores principales: Li, Shengqiang, Locke, Emily, Bruder, Joseph, Clarke, David, Doolan, Denise L., Havenga, Menzo J.E., Hill, Adrian V.S., Liljestrom, Peter, Monath, Thomas P., Naim, Hussein Y., Ockenhouse, Christian, Tang, De-chu C., Van Kampen, Kent R., Viret, Jean-Francois, Zavala, Fidel, Dubovsky, Filip
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7131149/
https://www.ncbi.nlm.nih.gov/pubmed/16914237
http://dx.doi.org/10.1016/j.vaccine.2006.07.035
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author Li, Shengqiang
Locke, Emily
Bruder, Joseph
Clarke, David
Doolan, Denise L.
Havenga, Menzo J.E.
Hill, Adrian V.S.
Liljestrom, Peter
Monath, Thomas P.
Naim, Hussein Y.
Ockenhouse, Christian
Tang, De-chu C.
Van Kampen, Kent R.
Viret, Jean-Francois
Zavala, Fidel
Dubovsky, Filip
author_facet Li, Shengqiang
Locke, Emily
Bruder, Joseph
Clarke, David
Doolan, Denise L.
Havenga, Menzo J.E.
Hill, Adrian V.S.
Liljestrom, Peter
Monath, Thomas P.
Naim, Hussein Y.
Ockenhouse, Christian
Tang, De-chu C.
Van Kampen, Kent R.
Viret, Jean-Francois
Zavala, Fidel
Dubovsky, Filip
author_sort Li, Shengqiang
collection PubMed
description A workshop on viral vectors for malaria vaccine development, organized by the PATH Malaria Vaccine Initiative, was held in Bethesda, MD on October 20, 2005. Recent advancements in viral-vectored malaria vaccine development and emerging vector technologies were presented and discussed. Classic viral vectors such as poxvirus, adenovirus and alphavirus vectors have been successfully used to deliver malaria antigens. Some of the vaccine candidates have demonstrated their potential in inducing malaria-specific immunity in animal models and human trials. In addition, emerging viral-vector technologies, such as measles virus (MV), vesicular stomatitis virus (VSV) and yellow fever (YF) virus, may also be useful for malaria vaccine development. Studies in animal models suggest that each viral vector is unique in its ability to induce humoral and/or cellular immune responses. Those studies have also revealed that optimization of Plasmodium genes for mammalian expression is an important aspect of vaccine design. Codon-optimization, surface-trafficking, de-glycosylation and removal of toxic domains can lead to improved immunogenicity. Understanding the vector's ability to induce an immune response and the expression of malaria antigens in mammalian cells will be critical in designing the next generation of viral-vectored malaria vaccines.
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spelling pubmed-71311492020-04-08 Viral vectors for malaria vaccine development Li, Shengqiang Locke, Emily Bruder, Joseph Clarke, David Doolan, Denise L. Havenga, Menzo J.E. Hill, Adrian V.S. Liljestrom, Peter Monath, Thomas P. Naim, Hussein Y. Ockenhouse, Christian Tang, De-chu C. Van Kampen, Kent R. Viret, Jean-Francois Zavala, Fidel Dubovsky, Filip Vaccine Article A workshop on viral vectors for malaria vaccine development, organized by the PATH Malaria Vaccine Initiative, was held in Bethesda, MD on October 20, 2005. Recent advancements in viral-vectored malaria vaccine development and emerging vector technologies were presented and discussed. Classic viral vectors such as poxvirus, adenovirus and alphavirus vectors have been successfully used to deliver malaria antigens. Some of the vaccine candidates have demonstrated their potential in inducing malaria-specific immunity in animal models and human trials. In addition, emerging viral-vector technologies, such as measles virus (MV), vesicular stomatitis virus (VSV) and yellow fever (YF) virus, may also be useful for malaria vaccine development. Studies in animal models suggest that each viral vector is unique in its ability to induce humoral and/or cellular immune responses. Those studies have also revealed that optimization of Plasmodium genes for mammalian expression is an important aspect of vaccine design. Codon-optimization, surface-trafficking, de-glycosylation and removal of toxic domains can lead to improved immunogenicity. Understanding the vector's ability to induce an immune response and the expression of malaria antigens in mammalian cells will be critical in designing the next generation of viral-vectored malaria vaccines. Elsevier Science 2007-03-30 2006-08-01 /pmc/articles/PMC7131149/ /pubmed/16914237 http://dx.doi.org/10.1016/j.vaccine.2006.07.035 Text en 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
Li, Shengqiang
Locke, Emily
Bruder, Joseph
Clarke, David
Doolan, Denise L.
Havenga, Menzo J.E.
Hill, Adrian V.S.
Liljestrom, Peter
Monath, Thomas P.
Naim, Hussein Y.
Ockenhouse, Christian
Tang, De-chu C.
Van Kampen, Kent R.
Viret, Jean-Francois
Zavala, Fidel
Dubovsky, Filip
Viral vectors for malaria vaccine development
title Viral vectors for malaria vaccine development
title_full Viral vectors for malaria vaccine development
title_fullStr Viral vectors for malaria vaccine development
title_full_unstemmed Viral vectors for malaria vaccine development
title_short Viral vectors for malaria vaccine development
title_sort viral vectors for malaria vaccine development
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7131149/
https://www.ncbi.nlm.nih.gov/pubmed/16914237
http://dx.doi.org/10.1016/j.vaccine.2006.07.035
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