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Engineered E. coli Nissle 1917 for delivery of bioactive IL-2 for cancer immunotherapy

In this study we performed a step-wise optimization of biologically active IL-2 for delivery using E. coli Nissle 1917. Engineering of the strain was coupled with an in vitro cell assay to measure the biological activity of microbially produced IL-2 (mi-IL2). Next, we assessed the immune modulatory...

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Autores principales: Tumas, Sarunas, Meldgaard, Trine Sundebo, Vaaben, Troels Holger, Suarez Hernandez, Sara, Rasmussen, Annemette Tengstedt, Vazquez-Uribe, Ruben, Hadrup, Sine Reker, Sommer, Morten O. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10397246/
https://www.ncbi.nlm.nih.gov/pubmed/37532747
http://dx.doi.org/10.1038/s41598-023-39365-2
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author Tumas, Sarunas
Meldgaard, Trine Sundebo
Vaaben, Troels Holger
Suarez Hernandez, Sara
Rasmussen, Annemette Tengstedt
Vazquez-Uribe, Ruben
Hadrup, Sine Reker
Sommer, Morten O. A.
author_facet Tumas, Sarunas
Meldgaard, Trine Sundebo
Vaaben, Troels Holger
Suarez Hernandez, Sara
Rasmussen, Annemette Tengstedt
Vazquez-Uribe, Ruben
Hadrup, Sine Reker
Sommer, Morten O. A.
author_sort Tumas, Sarunas
collection PubMed
description In this study we performed a step-wise optimization of biologically active IL-2 for delivery using E. coli Nissle 1917. Engineering of the strain was coupled with an in vitro cell assay to measure the biological activity of microbially produced IL-2 (mi-IL2). Next, we assessed the immune modulatory potential of mi-IL2 using a 3D tumor spheroid model demonstrating a strong effect on immune cell activation. Finally, we evaluated the anticancer properties of the engineered strain in a murine CT26 tumor model. The engineered strain was injected intravenously and selectively colonized tumors. The treatment was well-tolerated, and tumors of treated mice showed a modest reduction in tumor growth rate, as well as significantly elevated levels of IL-2 in the tumor. This work demonstrates a workflow for researchers interested in engineering E. coli Nissle for a new class of microbial therapy against cancer.
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spelling pubmed-103972462023-08-04 Engineered E. coli Nissle 1917 for delivery of bioactive IL-2 for cancer immunotherapy Tumas, Sarunas Meldgaard, Trine Sundebo Vaaben, Troels Holger Suarez Hernandez, Sara Rasmussen, Annemette Tengstedt Vazquez-Uribe, Ruben Hadrup, Sine Reker Sommer, Morten O. A. Sci Rep Article In this study we performed a step-wise optimization of biologically active IL-2 for delivery using E. coli Nissle 1917. Engineering of the strain was coupled with an in vitro cell assay to measure the biological activity of microbially produced IL-2 (mi-IL2). Next, we assessed the immune modulatory potential of mi-IL2 using a 3D tumor spheroid model demonstrating a strong effect on immune cell activation. Finally, we evaluated the anticancer properties of the engineered strain in a murine CT26 tumor model. The engineered strain was injected intravenously and selectively colonized tumors. The treatment was well-tolerated, and tumors of treated mice showed a modest reduction in tumor growth rate, as well as significantly elevated levels of IL-2 in the tumor. This work demonstrates a workflow for researchers interested in engineering E. coli Nissle for a new class of microbial therapy against cancer. Nature Publishing Group UK 2023-08-02 /pmc/articles/PMC10397246/ /pubmed/37532747 http://dx.doi.org/10.1038/s41598-023-39365-2 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Tumas, Sarunas
Meldgaard, Trine Sundebo
Vaaben, Troels Holger
Suarez Hernandez, Sara
Rasmussen, Annemette Tengstedt
Vazquez-Uribe, Ruben
Hadrup, Sine Reker
Sommer, Morten O. A.
Engineered E. coli Nissle 1917 for delivery of bioactive IL-2 for cancer immunotherapy
title Engineered E. coli Nissle 1917 for delivery of bioactive IL-2 for cancer immunotherapy
title_full Engineered E. coli Nissle 1917 for delivery of bioactive IL-2 for cancer immunotherapy
title_fullStr Engineered E. coli Nissle 1917 for delivery of bioactive IL-2 for cancer immunotherapy
title_full_unstemmed Engineered E. coli Nissle 1917 for delivery of bioactive IL-2 for cancer immunotherapy
title_short Engineered E. coli Nissle 1917 for delivery of bioactive IL-2 for cancer immunotherapy
title_sort engineered e. coli nissle 1917 for delivery of bioactive il-2 for cancer immunotherapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10397246/
https://www.ncbi.nlm.nih.gov/pubmed/37532747
http://dx.doi.org/10.1038/s41598-023-39365-2
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