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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...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2020
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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. |
format | Online Article Text |
id | pubmed-7113479 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
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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