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Immunotherapy with engineered bacteria by targeting the STING pathway for anti-tumor immunity

Synthetic biology is a powerful tool to create therapeutics which can be rationally designed to enable unique and combinatorial functionalities. Here we utilize non-pathogenic E coli Nissle as a versatile platform for the development of a living biotherapeutic for the treatment of cancer. The engine...

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Autores principales: Leventhal, Daniel S., Sokolovska, Anna, Li, Ning, Plescia, Christopher, Kolodziej, Starsha A., Gallant, Carey W., Christmas, Rudy, Gao, Jian-Rong, James, Michael J., Abin-Fuentes, Andres, Momin, Munira, Bergeron, Christopher, Fisher, Adam, Miller, Paul F., West, Kip A., Lora, Jose M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7264239/
https://www.ncbi.nlm.nih.gov/pubmed/32483165
http://dx.doi.org/10.1038/s41467-020-16602-0
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author Leventhal, Daniel S.
Sokolovska, Anna
Li, Ning
Plescia, Christopher
Kolodziej, Starsha A.
Gallant, Carey W.
Christmas, Rudy
Gao, Jian-Rong
James, Michael J.
Abin-Fuentes, Andres
Momin, Munira
Bergeron, Christopher
Fisher, Adam
Miller, Paul F.
West, Kip A.
Lora, Jose M.
author_facet Leventhal, Daniel S.
Sokolovska, Anna
Li, Ning
Plescia, Christopher
Kolodziej, Starsha A.
Gallant, Carey W.
Christmas, Rudy
Gao, Jian-Rong
James, Michael J.
Abin-Fuentes, Andres
Momin, Munira
Bergeron, Christopher
Fisher, Adam
Miller, Paul F.
West, Kip A.
Lora, Jose M.
author_sort Leventhal, Daniel S.
collection PubMed
description Synthetic biology is a powerful tool to create therapeutics which can be rationally designed to enable unique and combinatorial functionalities. Here we utilize non-pathogenic E coli Nissle as a versatile platform for the development of a living biotherapeutic for the treatment of cancer. The engineered bacterial strain, referred to as SYNB1891, targets STING-activation to phagocytic antigen-presenting cells (APCs) in the tumor and activates complementary innate immune pathways. SYNB1891 treatment results in efficacious antitumor immunity with the formation of immunological memory in murine tumor models and robust activation of human APCs. SYNB1891 is designed to meet manufacturability and regulatory requirements with built in biocontainment features which do not compromise its efficacy. This work provides a roadmap for the development of future therapeutics and demonstrates the transformative potential of synthetic biology for the treatment of human disease when drug development criteria are incorporated into the design process for a living medicine.
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spelling pubmed-72642392020-06-12 Immunotherapy with engineered bacteria by targeting the STING pathway for anti-tumor immunity Leventhal, Daniel S. Sokolovska, Anna Li, Ning Plescia, Christopher Kolodziej, Starsha A. Gallant, Carey W. Christmas, Rudy Gao, Jian-Rong James, Michael J. Abin-Fuentes, Andres Momin, Munira Bergeron, Christopher Fisher, Adam Miller, Paul F. West, Kip A. Lora, Jose M. Nat Commun Article Synthetic biology is a powerful tool to create therapeutics which can be rationally designed to enable unique and combinatorial functionalities. Here we utilize non-pathogenic E coli Nissle as a versatile platform for the development of a living biotherapeutic for the treatment of cancer. The engineered bacterial strain, referred to as SYNB1891, targets STING-activation to phagocytic antigen-presenting cells (APCs) in the tumor and activates complementary innate immune pathways. SYNB1891 treatment results in efficacious antitumor immunity with the formation of immunological memory in murine tumor models and robust activation of human APCs. SYNB1891 is designed to meet manufacturability and regulatory requirements with built in biocontainment features which do not compromise its efficacy. This work provides a roadmap for the development of future therapeutics and demonstrates the transformative potential of synthetic biology for the treatment of human disease when drug development criteria are incorporated into the design process for a living medicine. Nature Publishing Group UK 2020-06-01 /pmc/articles/PMC7264239/ /pubmed/32483165 http://dx.doi.org/10.1038/s41467-020-16602-0 Text en © The Author(s) 2020 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Leventhal, Daniel S.
Sokolovska, Anna
Li, Ning
Plescia, Christopher
Kolodziej, Starsha A.
Gallant, Carey W.
Christmas, Rudy
Gao, Jian-Rong
James, Michael J.
Abin-Fuentes, Andres
Momin, Munira
Bergeron, Christopher
Fisher, Adam
Miller, Paul F.
West, Kip A.
Lora, Jose M.
Immunotherapy with engineered bacteria by targeting the STING pathway for anti-tumor immunity
title Immunotherapy with engineered bacteria by targeting the STING pathway for anti-tumor immunity
title_full Immunotherapy with engineered bacteria by targeting the STING pathway for anti-tumor immunity
title_fullStr Immunotherapy with engineered bacteria by targeting the STING pathway for anti-tumor immunity
title_full_unstemmed Immunotherapy with engineered bacteria by targeting the STING pathway for anti-tumor immunity
title_short Immunotherapy with engineered bacteria by targeting the STING pathway for anti-tumor immunity
title_sort immunotherapy with engineered bacteria by targeting the sting pathway for anti-tumor immunity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7264239/
https://www.ncbi.nlm.nih.gov/pubmed/32483165
http://dx.doi.org/10.1038/s41467-020-16602-0
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