Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Tzeng, Stephany Y., Patel, Kisha K., Wilson, David R., Meyer, Randall A., Rhodes, Kelly R., Green, Jordan J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2020
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
_version_ 1783502380436815872
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
work_keys_str_mv AT tzengstephanyy insitugeneticengineeringoftumorsforlonglastingandsystemicimmunotherapy
AT patelkishak insitugeneticengineeringoftumorsforlonglastingandsystemicimmunotherapy
AT wilsondavidr insitugeneticengineeringoftumorsforlonglastingandsystemicimmunotherapy
AT meyerrandalla insitugeneticengineeringoftumorsforlonglastingandsystemicimmunotherapy
AT rhodeskellyr insitugeneticengineeringoftumorsforlonglastingandsystemicimmunotherapy
AT greenjordanj insitugeneticengineeringoftumorsforlonglastingandsystemicimmunotherapy