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In situ genetic engineering of tumors for long-lasting and systemic immunotherapy
Cancer immunotherapy has been the subject of extensive research, but highly effective and broadly applicable methods remain elusive. Moreover, a general approach to engender endogenous patient-specific cellular therapy, without the need for a priori knowledge of tumor antigen, ex vivo cellular manip...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7049107/ https://www.ncbi.nlm.nih.gov/pubmed/32034097 http://dx.doi.org/10.1073/pnas.1916039117 |
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author | Tzeng, Stephany Y. Patel, Kisha K. Wilson, David R. Meyer, Randall A. Rhodes, Kelly R. Green, Jordan J. |
author_facet | Tzeng, Stephany Y. Patel, Kisha K. Wilson, David R. Meyer, Randall A. Rhodes, Kelly R. Green, Jordan J. |
author_sort | Tzeng, Stephany Y. |
collection | PubMed |
description | Cancer immunotherapy has been the subject of extensive research, but highly effective and broadly applicable methods remain elusive. Moreover, a general approach to engender endogenous patient-specific cellular therapy, without the need for a priori knowledge of tumor antigen, ex vivo cellular manipulation, or cellular manufacture, could dramatically reduce costs and broaden accessibility. Here, we describe a biotechnology based on synthetic, biodegradable nanoparticles that can genetically reprogram cancer cells and their microenvironment in situ so that the cancer cells can act as tumor-associated antigen-presenting cells (tAPCs) by inducing coexpression of a costimulatory molecule (4-1BBL) and immunostimulatory cytokine (IL-12). In B16-F10 melanoma and MC38 colorectal carcinoma mouse models, reprogramming nanoparticles in combination with checkpoint blockade significantly reduced tumor growth over time and, in some cases, cleared the tumor, leading to long-term survivors that were then resistant to the formation of new tumors upon rechallenge at a distant site. In vitro and in vivo analyses confirmed that locally delivered tAPC-reprogramming nanoparticles led to a significant cell-mediated cytotoxic immune response with systemic effects. The systemic tumor-specific and cell-mediated immunotherapy response was achieved without requiring a priori knowledge of tumor-expressed antigens and reflects the translational potential of this nanomedicine. |
format | Online Article Text |
id | pubmed-7049107 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-70491072020-03-06 In situ genetic engineering of tumors for long-lasting and systemic immunotherapy Tzeng, Stephany Y. Patel, Kisha K. Wilson, David R. Meyer, Randall A. Rhodes, Kelly R. Green, Jordan J. Proc Natl Acad Sci U S A Biological Sciences Cancer immunotherapy has been the subject of extensive research, but highly effective and broadly applicable methods remain elusive. Moreover, a general approach to engender endogenous patient-specific cellular therapy, without the need for a priori knowledge of tumor antigen, ex vivo cellular manipulation, or cellular manufacture, could dramatically reduce costs and broaden accessibility. Here, we describe a biotechnology based on synthetic, biodegradable nanoparticles that can genetically reprogram cancer cells and their microenvironment in situ so that the cancer cells can act as tumor-associated antigen-presenting cells (tAPCs) by inducing coexpression of a costimulatory molecule (4-1BBL) and immunostimulatory cytokine (IL-12). In B16-F10 melanoma and MC38 colorectal carcinoma mouse models, reprogramming nanoparticles in combination with checkpoint blockade significantly reduced tumor growth over time and, in some cases, cleared the tumor, leading to long-term survivors that were then resistant to the formation of new tumors upon rechallenge at a distant site. In vitro and in vivo analyses confirmed that locally delivered tAPC-reprogramming nanoparticles led to a significant cell-mediated cytotoxic immune response with systemic effects. The systemic tumor-specific and cell-mediated immunotherapy response was achieved without requiring a priori knowledge of tumor-expressed antigens and reflects the translational potential of this nanomedicine. National Academy of Sciences 2020-02-25 2020-02-07 /pmc/articles/PMC7049107/ /pubmed/32034097 http://dx.doi.org/10.1073/pnas.1916039117 Text en Copyright © 2020 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) . |
spellingShingle | Biological Sciences Tzeng, Stephany Y. Patel, Kisha K. Wilson, David R. Meyer, Randall A. Rhodes, Kelly R. Green, Jordan J. In situ genetic engineering of tumors for long-lasting and systemic immunotherapy |
title | In situ genetic engineering of tumors for long-lasting and systemic immunotherapy |
title_full | In situ genetic engineering of tumors for long-lasting and systemic immunotherapy |
title_fullStr | In situ genetic engineering of tumors for long-lasting and systemic immunotherapy |
title_full_unstemmed | In situ genetic engineering of tumors for long-lasting and systemic immunotherapy |
title_short | In situ genetic engineering of tumors for long-lasting and systemic immunotherapy |
title_sort | in situ genetic engineering of tumors for long-lasting and systemic immunotherapy |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7049107/ https://www.ncbi.nlm.nih.gov/pubmed/32034097 http://dx.doi.org/10.1073/pnas.1916039117 |
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