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Intratumoral delivered novel circular mRNA encoding cytokines for immune modulation and cancer therapy
The success of the two mRNA vaccines developed by Moderna and BioNTech during the COVID-19 pandemic increased research interest into the application of mRNA technologies. Compared with the canonical linear mRNA used in these vaccines, circular mRNA has been found to mediate more potent and durable p...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Gene & Cell Therapy
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9482165/ https://www.ncbi.nlm.nih.gov/pubmed/36156907 http://dx.doi.org/10.1016/j.omtn.2022.09.010 |
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author | Yang, Jiali Zhu, Jiafeng Sun, Jiaojiao Chen, Yiyun Du, Yaran Tan, Yiling Wu, Linpeng Zhai, Mengting Wei, Lixiang Li, Na Huang, Ke Hou, Qiangbo Tong, Zhenbo Bechthold, Andreas Tian, Hao Sun, Zhenhua Zuo, Chijian |
author_facet | Yang, Jiali Zhu, Jiafeng Sun, Jiaojiao Chen, Yiyun Du, Yaran Tan, Yiling Wu, Linpeng Zhai, Mengting Wei, Lixiang Li, Na Huang, Ke Hou, Qiangbo Tong, Zhenbo Bechthold, Andreas Tian, Hao Sun, Zhenhua Zuo, Chijian |
author_sort | Yang, Jiali |
collection | PubMed |
description | The success of the two mRNA vaccines developed by Moderna and BioNTech during the COVID-19 pandemic increased research interest into the application of mRNA technologies. Compared with the canonical linear mRNA used in these vaccines, circular mRNA has been found to mediate more potent and durable protein expression and demands a simpler manufacturing procedure. However, the application of circular mRNA is still at the initiation stage, and proof of concept for its use as a future medicine or vaccine is required. In the current study, we established a novel type of circular mRNA, termed cmRNA, based on the echovirus 29-derived internal ribosome entry site element and newly designed homology arms and RNA spacers. Our results demonstrated that this type of circular mRNA could mediate strong and durable expression of various types of proteins, compared with typical linear mRNA. Moreover, for the first time, our study demonstrated that direct intratumoral administration of cmRNA encoding a mixture of cytokines achieved successful modulation of intratumoral and systematic anti-tumor immune responses and enhanced anti-programmed cell death protein 1 (PD-1) antibody-induced tumor repression in a syngeneic mouse model. This novel circular mRNA platform is thereby suitable for direct intratumoral administration for cancer therapy. |
format | Online Article Text |
id | pubmed-9482165 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Society of Gene & Cell Therapy |
record_format | MEDLINE/PubMed |
spelling | pubmed-94821652022-09-19 Intratumoral delivered novel circular mRNA encoding cytokines for immune modulation and cancer therapy Yang, Jiali Zhu, Jiafeng Sun, Jiaojiao Chen, Yiyun Du, Yaran Tan, Yiling Wu, Linpeng Zhai, Mengting Wei, Lixiang Li, Na Huang, Ke Hou, Qiangbo Tong, Zhenbo Bechthold, Andreas Tian, Hao Sun, Zhenhua Zuo, Chijian Mol Ther Nucleic Acids Original Article The success of the two mRNA vaccines developed by Moderna and BioNTech during the COVID-19 pandemic increased research interest into the application of mRNA technologies. Compared with the canonical linear mRNA used in these vaccines, circular mRNA has been found to mediate more potent and durable protein expression and demands a simpler manufacturing procedure. However, the application of circular mRNA is still at the initiation stage, and proof of concept for its use as a future medicine or vaccine is required. In the current study, we established a novel type of circular mRNA, termed cmRNA, based on the echovirus 29-derived internal ribosome entry site element and newly designed homology arms and RNA spacers. Our results demonstrated that this type of circular mRNA could mediate strong and durable expression of various types of proteins, compared with typical linear mRNA. Moreover, for the first time, our study demonstrated that direct intratumoral administration of cmRNA encoding a mixture of cytokines achieved successful modulation of intratumoral and systematic anti-tumor immune responses and enhanced anti-programmed cell death protein 1 (PD-1) antibody-induced tumor repression in a syngeneic mouse model. This novel circular mRNA platform is thereby suitable for direct intratumoral administration for cancer therapy. American Society of Gene & Cell Therapy 2022-09-17 /pmc/articles/PMC9482165/ /pubmed/36156907 http://dx.doi.org/10.1016/j.omtn.2022.09.010 Text en © 2022 The Authors https://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 | Original Article Yang, Jiali Zhu, Jiafeng Sun, Jiaojiao Chen, Yiyun Du, Yaran Tan, Yiling Wu, Linpeng Zhai, Mengting Wei, Lixiang Li, Na Huang, Ke Hou, Qiangbo Tong, Zhenbo Bechthold, Andreas Tian, Hao Sun, Zhenhua Zuo, Chijian Intratumoral delivered novel circular mRNA encoding cytokines for immune modulation and cancer therapy |
title | Intratumoral delivered novel circular mRNA encoding cytokines for immune modulation and cancer therapy |
title_full | Intratumoral delivered novel circular mRNA encoding cytokines for immune modulation and cancer therapy |
title_fullStr | Intratumoral delivered novel circular mRNA encoding cytokines for immune modulation and cancer therapy |
title_full_unstemmed | Intratumoral delivered novel circular mRNA encoding cytokines for immune modulation and cancer therapy |
title_short | Intratumoral delivered novel circular mRNA encoding cytokines for immune modulation and cancer therapy |
title_sort | intratumoral delivered novel circular mrna encoding cytokines for immune modulation and cancer therapy |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9482165/ https://www.ncbi.nlm.nih.gov/pubmed/36156907 http://dx.doi.org/10.1016/j.omtn.2022.09.010 |
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