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Engineering Cellular Biosensors with Customizable Antiviral Responses Targeting Hepatitis B Virus

SynNotch receptor technology is a versatile tool that uses the regulatory notch core portion with an extracellular scFv and an intracellular transcription factor that enables to program customized input and output functions in mammalian cells. In this study, we designed a novel synNotch receptor com...

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Autores principales: Matsunaga, Satoko, Jeremiah, Sundararaj S., Miyakawa, Kei, Kurotaki, Daisuke, Shizukuishi, Sayaka, Watashi, Koichi, Nishitsuji, Hironori, Kimura, Hirokazu, Tamura, Tomohiko, Yamamoto, Naoki, Shimotohno, Kunitada, Wakita, Takaji, Ryo, Akihide
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113479/
https://www.ncbi.nlm.nih.gov/pubmed/32105634
http://dx.doi.org/10.1016/j.isci.2020.100867
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author Matsunaga, Satoko
Jeremiah, Sundararaj S.
Miyakawa, Kei
Kurotaki, Daisuke
Shizukuishi, Sayaka
Watashi, Koichi
Nishitsuji, Hironori
Kimura, Hirokazu
Tamura, Tomohiko
Yamamoto, Naoki
Shimotohno, Kunitada
Wakita, Takaji
Ryo, Akihide
author_facet Matsunaga, Satoko
Jeremiah, Sundararaj S.
Miyakawa, Kei
Kurotaki, Daisuke
Shizukuishi, Sayaka
Watashi, Koichi
Nishitsuji, Hironori
Kimura, Hirokazu
Tamura, Tomohiko
Yamamoto, Naoki
Shimotohno, Kunitada
Wakita, Takaji
Ryo, Akihide
author_sort Matsunaga, Satoko
collection PubMed
description SynNotch receptor technology is a versatile tool that uses the regulatory notch core portion with an extracellular scFv and an intracellular transcription factor that enables to program customized input and output functions in mammalian cells. In this study, we designed a novel synNotch receptor comprising scFv against HBs antigen linked with an intracellular artificial transcription factor and exploited it for viral sensing and cellular immunotherapy. The synNotch receptor expressing cells sensed HBV particles and membrane-bound HBs antigens and responded by expressing reporter molecules, secNL or GFP. We also programmed these cells to dispense antiviral responses such as type I interferon and anti-HBV neutralizing mouse-human chimeric antibodies. Our data reveal that synNotch receptor signaling works for membrane-bound ligands such as enveloped viral particles and proteins borne on liposomal vesicles. This study establishes the concepts of “engineered immunity” where the synNotch platform is utilized for cellular immunotherapy against viral infections.
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spelling pubmed-71134792020-04-03 Engineering Cellular Biosensors with Customizable Antiviral Responses Targeting Hepatitis B Virus Matsunaga, Satoko Jeremiah, Sundararaj S. Miyakawa, Kei Kurotaki, Daisuke Shizukuishi, Sayaka Watashi, Koichi Nishitsuji, Hironori Kimura, Hirokazu Tamura, Tomohiko Yamamoto, Naoki Shimotohno, Kunitada Wakita, Takaji Ryo, Akihide iScience Article SynNotch receptor technology is a versatile tool that uses the regulatory notch core portion with an extracellular scFv and an intracellular transcription factor that enables to program customized input and output functions in mammalian cells. In this study, we designed a novel synNotch receptor comprising scFv against HBs antigen linked with an intracellular artificial transcription factor and exploited it for viral sensing and cellular immunotherapy. The synNotch receptor expressing cells sensed HBV particles and membrane-bound HBs antigens and responded by expressing reporter molecules, secNL or GFP. We also programmed these cells to dispense antiviral responses such as type I interferon and anti-HBV neutralizing mouse-human chimeric antibodies. Our data reveal that synNotch receptor signaling works for membrane-bound ligands such as enveloped viral particles and proteins borne on liposomal vesicles. This study establishes the concepts of “engineered immunity” where the synNotch platform is utilized for cellular immunotherapy against viral infections. Elsevier 2020-02-26 /pmc/articles/PMC7113479/ /pubmed/32105634 http://dx.doi.org/10.1016/j.isci.2020.100867 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Matsunaga, Satoko
Jeremiah, Sundararaj S.
Miyakawa, Kei
Kurotaki, Daisuke
Shizukuishi, Sayaka
Watashi, Koichi
Nishitsuji, Hironori
Kimura, Hirokazu
Tamura, Tomohiko
Yamamoto, Naoki
Shimotohno, Kunitada
Wakita, Takaji
Ryo, Akihide
Engineering Cellular Biosensors with Customizable Antiviral Responses Targeting Hepatitis B Virus
title Engineering Cellular Biosensors with Customizable Antiviral Responses Targeting Hepatitis B Virus
title_full Engineering Cellular Biosensors with Customizable Antiviral Responses Targeting Hepatitis B Virus
title_fullStr Engineering Cellular Biosensors with Customizable Antiviral Responses Targeting Hepatitis B Virus
title_full_unstemmed Engineering Cellular Biosensors with Customizable Antiviral Responses Targeting Hepatitis B Virus
title_short Engineering Cellular Biosensors with Customizable Antiviral Responses Targeting Hepatitis B Virus
title_sort engineering cellular biosensors with customizable antiviral responses targeting hepatitis b virus
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7113479/
https://www.ncbi.nlm.nih.gov/pubmed/32105634
http://dx.doi.org/10.1016/j.isci.2020.100867
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