Cargando…

Nano‐optogenetic immunotherapy

Chimeric antigen receptor (CAR) T cell‐based immunotherapy has been increasingly used in the clinic for cancer intervention over the past 5 years. CAR T‐cell therapy takes advantage of genetically‐modified T cells to express synthetic CAR molecules on the cell surface. To date, up to six CAR T cell...

Descripción completa

Detalles Bibliográficos
Autores principales: Huang, Kai, Liu, Xiaoxuan, Han, Gang, Zhou, Yubin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9471049/
https://www.ncbi.nlm.nih.gov/pubmed/36101937
http://dx.doi.org/10.1002/ctm2.1020
_version_ 1784788979579617280
author Huang, Kai
Liu, Xiaoxuan
Han, Gang
Zhou, Yubin
author_facet Huang, Kai
Liu, Xiaoxuan
Han, Gang
Zhou, Yubin
author_sort Huang, Kai
collection PubMed
description Chimeric antigen receptor (CAR) T cell‐based immunotherapy has been increasingly used in the clinic for cancer intervention over the past 5 years. CAR T‐cell therapy takes advantage of genetically‐modified T cells to express synthetic CAR molecules on the cell surface. To date, up to six CAR T cell therapy products have been approved by the Food and Drug Administration for the treatment of leukaemia, lymphoma, and multiple myeloma. In addition, hundreds of CAR‐T products are currently under clinical trials to treat solid tumours. In both the fundamental research and clinical applications, CAR T cell immunotherapy has achieved exciting progress with remarkable remission or suppression of cancers. However, CAR T cell‐based immunotherapy still faces significant safety issues, as exemplified by “on‐target off‐tumour” cytotoxicity due to lack of strict antigen specificity. In addition, uncontrolled massive activation of infused CAR T cells may create severe systemic inflammation with cytokine release syndrome and neurotoxicity. These challenges call for a need to combine nanotechnology and optogenetics with immunoengineering to develop spatiotemporally‐controllable CAR T cells, which enable wireless photo‐tunable activation of therapeutic immune cells to deliver personalised therapy in the tumour microenvironment.
format Online
Article
Text
id pubmed-9471049
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-94710492022-09-28 Nano‐optogenetic immunotherapy Huang, Kai Liu, Xiaoxuan Han, Gang Zhou, Yubin Clin Transl Med Commentary Chimeric antigen receptor (CAR) T cell‐based immunotherapy has been increasingly used in the clinic for cancer intervention over the past 5 years. CAR T‐cell therapy takes advantage of genetically‐modified T cells to express synthetic CAR molecules on the cell surface. To date, up to six CAR T cell therapy products have been approved by the Food and Drug Administration for the treatment of leukaemia, lymphoma, and multiple myeloma. In addition, hundreds of CAR‐T products are currently under clinical trials to treat solid tumours. In both the fundamental research and clinical applications, CAR T cell immunotherapy has achieved exciting progress with remarkable remission or suppression of cancers. However, CAR T cell‐based immunotherapy still faces significant safety issues, as exemplified by “on‐target off‐tumour” cytotoxicity due to lack of strict antigen specificity. In addition, uncontrolled massive activation of infused CAR T cells may create severe systemic inflammation with cytokine release syndrome and neurotoxicity. These challenges call for a need to combine nanotechnology and optogenetics with immunoengineering to develop spatiotemporally‐controllable CAR T cells, which enable wireless photo‐tunable activation of therapeutic immune cells to deliver personalised therapy in the tumour microenvironment. John Wiley and Sons Inc. 2022-09-13 /pmc/articles/PMC9471049/ /pubmed/36101937 http://dx.doi.org/10.1002/ctm2.1020 Text en © 2022 The Authors. Clinical and Translational Medicine published by John Wiley & Sons Australia, Ltd on behalf of Shanghai Institute of Clinical Bioinformatics. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Commentary
Huang, Kai
Liu, Xiaoxuan
Han, Gang
Zhou, Yubin
Nano‐optogenetic immunotherapy
title Nano‐optogenetic immunotherapy
title_full Nano‐optogenetic immunotherapy
title_fullStr Nano‐optogenetic immunotherapy
title_full_unstemmed Nano‐optogenetic immunotherapy
title_short Nano‐optogenetic immunotherapy
title_sort nano‐optogenetic immunotherapy
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9471049/
https://www.ncbi.nlm.nih.gov/pubmed/36101937
http://dx.doi.org/10.1002/ctm2.1020
work_keys_str_mv AT huangkai nanooptogeneticimmunotherapy
AT liuxiaoxuan nanooptogeneticimmunotherapy
AT hangang nanooptogeneticimmunotherapy
AT zhouyubin nanooptogeneticimmunotherapy