Chapter Graphene and Active Metamaterials: Theoretical Methods and Physical Properties

Protective immune defences are dependent upon critical roles played by dendritic cells (DCs), rendering them important targets for both vaccine delivery and virus infection. Studies in these areas led to successful development of targeted vaccine delivery, including synthetic virus-like particle (SV...

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Main Authors: Mattheakis, Marios, Kaxiras, Efthimios, Tsironis, G. P.
Format: Online
Jezik:angleščina
Izdano: InTechOpen 2021
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Online dostop:ONIX_20210602_10.5772/67900_303
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author Mattheakis, Marios
Kaxiras, Efthimios
Tsironis, G. P.
author_browse Kaxiras, Efthimios
Mattheakis, Marios
Tsironis, G. P.
author_facet Mattheakis, Marios
Kaxiras, Efthimios
Tsironis, G. P.
author_sort Mattheakis, Marios
collection Directory of Open Access Books
description Protective immune defences are dependent upon critical roles played by dendritic cells (DCs), rendering them important targets for both vaccine delivery and virus infection. Studies in these areas led to successful development of targeted vaccine delivery, including synthetic virus-like particle (SVLP) and nanoparticulate RNA vaccines. A major consideration is DC endocytosis, whereby the different endocytic routes influencing the outcome. Rapid clathrin-mediated endocytosis likely favours degradative pathways. Slower processes such as macropinocytosis, caveolar endocytosis and retrograde transport to endoplasmic reticulum relate more to the processing rates leading to antigen presentation by DCs. These pathways are also influential in promoting the initiation of virus replication following infection. DC endocytosis of RNA viruses and RNA vaccines must lead to cytosolic translocation of the RNA for translation, relating to the process of antigen cross-presentation. One can learn from observations on both virus infections and cross-presentation for delivering RNA vaccines. Accordingly, recent advances in nanoparticulate delivery have been applied with self-amplifying replicon RNA (RepRNA), providing efficient delivery to DCs and promoting replicon-encoded antigen translation. Through realising the important relationships between DC endocytic pathways and induction of immune responses, delivery of SVLP and RepRNA vaccines to DCs offers high value for the development of future synthetic vaccine platforms.
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spelling doab-20.500.12854ir-706322024-03-31T22:43:51Z Chapter Graphene and Active Metamaterials: Theoretical Methods and Physical Properties Mattheakis, Marios Kaxiras, Efthimios Tsironis, G. P. dendritic cells, endocytosis, virus infection, vaccines, SVLPs, self-amplifying RNA thema EDItEUR::M Medicine and Nursing::MJ Clinical and internal medicine::MJC Diseases and disorders::MJCM Immunology Protective immune defences are dependent upon critical roles played by dendritic cells (DCs), rendering them important targets for both vaccine delivery and virus infection. Studies in these areas led to successful development of targeted vaccine delivery, including synthetic virus-like particle (SVLP) and nanoparticulate RNA vaccines. A major consideration is DC endocytosis, whereby the different endocytic routes influencing the outcome. Rapid clathrin-mediated endocytosis likely favours degradative pathways. Slower processes such as macropinocytosis, caveolar endocytosis and retrograde transport to endoplasmic reticulum relate more to the processing rates leading to antigen presentation by DCs. These pathways are also influential in promoting the initiation of virus replication following infection. DC endocytosis of RNA viruses and RNA vaccines must lead to cytosolic translocation of the RNA for translation, relating to the process of antigen cross-presentation. One can learn from observations on both virus infections and cross-presentation for delivering RNA vaccines. Accordingly, recent advances in nanoparticulate delivery have been applied with self-amplifying replicon RNA (RepRNA), providing efficient delivery to DCs and promoting replicon-encoded antigen translation. Through realising the important relationships between DC endocytic pathways and induction of immune responses, delivery of SVLP and RepRNA vaccines to DCs offers high value for the development of future synthetic vaccine platforms. 2021-02-10T12:58:18Z 2021-06-02T10:08:59Z 2017 chapter ONIX_20210602_10.5772/67900_303 https://library.oapen.org/handle/20.500.12657/49189 https://directory.doabooks.org/handle/20.500.12854/70632 eng open access image/jpeg image/jpeg n/a n/a https://library.oapen.org/bitstream/20.500.12657/49189/1/54822.pdf https://library.oapen.org/bitstream/20.500.12657/49189/1/54822.pdf InTechOpen 10.5772/67900 10.5772/67900 035ecc65-6737-43cf-a13a-6bdf67ce01f4 open access
spellingShingle dendritic cells, endocytosis, virus infection, vaccines, SVLPs, self-amplifying RNA
thema EDItEUR::M Medicine and Nursing::MJ Clinical and internal medicine::MJC Diseases and disorders::MJCM Immunology
Mattheakis, Marios
Kaxiras, Efthimios
Tsironis, G. P.
Chapter Graphene and Active Metamaterials: Theoretical Methods and Physical Properties
title Chapter Graphene and Active Metamaterials: Theoretical Methods and Physical Properties
title_full Chapter Graphene and Active Metamaterials: Theoretical Methods and Physical Properties
title_fullStr Chapter Graphene and Active Metamaterials: Theoretical Methods and Physical Properties
title_full_unstemmed Chapter Graphene and Active Metamaterials: Theoretical Methods and Physical Properties
title_short Chapter Graphene and Active Metamaterials: Theoretical Methods and Physical Properties
title_sort chapter graphene and active metamaterials theoretical methods and physical properties
topic dendritic cells, endocytosis, virus infection, vaccines, SVLPs, self-amplifying RNA
thema EDItEUR::M Medicine and Nursing::MJ Clinical and internal medicine::MJC Diseases and disorders::MJCM Immunology
topic_facet dendritic cells, endocytosis, virus infection, vaccines, SVLPs, self-amplifying RNA
thema EDItEUR::M Medicine and Nursing::MJ Clinical and internal medicine::MJC Diseases and disorders::MJCM Immunology
url ONIX_20210602_10.5772/67900_303
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