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Infection-Mimicking Materials to Program Dendritic Cells In Situ

Cancer vaccines typically depend on cumbersome and expensive manipulation of cells in the laboratory, and subsequent cell transplantation leads to poor lymph node homing and limited efficacy. We propose that materials mimicking key aspects of bacterial infection may instead be used to directly contr...

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Detalles Bibliográficos
Autores principales: Ali, Omar A., Huebsch, Nathaniel, Cao, Lan, Dranoff, Glenn, Mooney, David J.
Formato: Texto
Lenguaje:English
Publicado: 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2684978/
https://www.ncbi.nlm.nih.gov/pubmed/19136947
http://dx.doi.org/10.1038/nmat2357
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author Ali, Omar A.
Huebsch, Nathaniel
Cao, Lan
Dranoff, Glenn
Mooney, David J.
author_facet Ali, Omar A.
Huebsch, Nathaniel
Cao, Lan
Dranoff, Glenn
Mooney, David J.
author_sort Ali, Omar A.
collection PubMed
description Cancer vaccines typically depend on cumbersome and expensive manipulation of cells in the laboratory, and subsequent cell transplantation leads to poor lymph node homing and limited efficacy. We propose that materials mimicking key aspects of bacterial infection may instead be used to directly control immune cell trafficking and activation in the body. It is demonstrated that polymers can be designed to first release a cytokine to recruit and house host dendritic cells (DCs), and subsequently present cancer antigens and danger signals to activate the resident DCs and dramatically enhance their homing to lymph nodes. Specific and protective anti-tumor immunity was generated with these materials, as 90% survival was achieved in animals that otherwise die from cancer within 25 days. These materials show promise as cancer vaccines, and more broadly suggest that polymers may be designed to program and control the trafficking of a variety of cell types in the body.
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spelling pubmed-26849782009-08-01 Infection-Mimicking Materials to Program Dendritic Cells In Situ Ali, Omar A. Huebsch, Nathaniel Cao, Lan Dranoff, Glenn Mooney, David J. Nat Mater Article Cancer vaccines typically depend on cumbersome and expensive manipulation of cells in the laboratory, and subsequent cell transplantation leads to poor lymph node homing and limited efficacy. We propose that materials mimicking key aspects of bacterial infection may instead be used to directly control immune cell trafficking and activation in the body. It is demonstrated that polymers can be designed to first release a cytokine to recruit and house host dendritic cells (DCs), and subsequently present cancer antigens and danger signals to activate the resident DCs and dramatically enhance their homing to lymph nodes. Specific and protective anti-tumor immunity was generated with these materials, as 90% survival was achieved in animals that otherwise die from cancer within 25 days. These materials show promise as cancer vaccines, and more broadly suggest that polymers may be designed to program and control the trafficking of a variety of cell types in the body. 2009-01-11 2009-02 /pmc/articles/PMC2684978/ /pubmed/19136947 http://dx.doi.org/10.1038/nmat2357 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Ali, Omar A.
Huebsch, Nathaniel
Cao, Lan
Dranoff, Glenn
Mooney, David J.
Infection-Mimicking Materials to Program Dendritic Cells In Situ
title Infection-Mimicking Materials to Program Dendritic Cells In Situ
title_full Infection-Mimicking Materials to Program Dendritic Cells In Situ
title_fullStr Infection-Mimicking Materials to Program Dendritic Cells In Situ
title_full_unstemmed Infection-Mimicking Materials to Program Dendritic Cells In Situ
title_short Infection-Mimicking Materials to Program Dendritic Cells In Situ
title_sort infection-mimicking materials to program dendritic cells in situ
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2684978/
https://www.ncbi.nlm.nih.gov/pubmed/19136947
http://dx.doi.org/10.1038/nmat2357
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