Cargando…
Intratumoral delivery of TransCon(™) TLR7/8 Agonist promotes sustained anti-tumor activity and local immune cell activation while minimizing systemic cytokine induction
BACKGROUND: Intratumoral (IT) delivery of toll-like receptor (TLR) agonists has shown encouraging anti-tumor benefit in preclinical and early clinical studies. However, IT delivery of TLR agonists may lead to rapid effusion from the tumor microenvironment (TME), potentially limiting the duration of...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9484246/ https://www.ncbi.nlm.nih.gov/pubmed/36123697 http://dx.doi.org/10.1186/s12935-022-02708-6 |
_version_ | 1784791841069072384 |
---|---|
author | Zúñiga, Luis Alejandro Leßmann, Torben Uppal, Karan Bisek, Nicola Hong, Enping Rasmussen, Caroline E. Karlsson, Jens-Jakob Zettler, Joachim Holten-Andersen, Lars Bang, Kathy Thakar, Dhruv Lee, Yu-Chi Martinez, Salomon Sabharwal, Simran Singh Stark, Sebastian Faltinger, Frank Kracker, Oliver Weisbrod, Samuel Müller, Robin Voigt, Tobias Bigott, Kornelia Tabrizifard, Mohammad Breinholt, Vibeke Miller Mirza, Amer M. Rosen, David B. Sprogøe, Kennett Punnonen, Juha |
author_facet | Zúñiga, Luis Alejandro Leßmann, Torben Uppal, Karan Bisek, Nicola Hong, Enping Rasmussen, Caroline E. Karlsson, Jens-Jakob Zettler, Joachim Holten-Andersen, Lars Bang, Kathy Thakar, Dhruv Lee, Yu-Chi Martinez, Salomon Sabharwal, Simran Singh Stark, Sebastian Faltinger, Frank Kracker, Oliver Weisbrod, Samuel Müller, Robin Voigt, Tobias Bigott, Kornelia Tabrizifard, Mohammad Breinholt, Vibeke Miller Mirza, Amer M. Rosen, David B. Sprogøe, Kennett Punnonen, Juha |
author_sort | Zúñiga, Luis Alejandro |
collection | PubMed |
description | BACKGROUND: Intratumoral (IT) delivery of toll-like receptor (TLR) agonists has shown encouraging anti-tumor benefit in preclinical and early clinical studies. However, IT delivery of TLR agonists may lead to rapid effusion from the tumor microenvironment (TME), potentially limiting the duration of local inflammation and increasing the risk of systemic adverse events. METHODS: To address these limitations, TransCon(™) TLR7/8 Agonist—an investigational sustained-release prodrug of resiquimod that uses a TransCon linker and hydrogel technology to achieve sustained and predictable IT release of resiquimod—was developed. TransCon TLR7/8 Agonist was characterized for resiquimod release in vitro and in vivo, in mice and rats, and was assessed for anti-tumor efficacy and pharmacodynamic activity in mice. RESULTS: Following a single IT dose, TransCon TLR7/8 Agonist mediated potent tumor growth inhibition which was associated with sustained resiquimod release over several weeks with minimal induction of systemic cytokines. TransCon TLR7/8 Agonist monotherapy promoted activation of antigen-presenting cells in the TME and tumor-draining lymph nodes, with evidence of activation and expansion of CD8(+) T cells in the tumor-draining lymph node and TME. Combination of TransCon TLR7/8 Agonist with systemic immunotherapy further promoted anti-tumor activity in TransCon TLR7/8 Agonist-treated tumors. In a bilateral tumor setting, combination of TransCon TLR7/8 Agonist with systemic IL-2 potentiated tumor growth inhibition in both injected and non-injected tumors and conferred protection against tumor rechallenge following complete regressions. CONCLUSIONS: Our findings show that a single dose of TransCon TLR7/8 Agonist can mediate sustained local release of resiquimod in the TME and promote potent anti-tumor effects as monotherapy and in combination with systemic immunotherapy, supporting TransCon TLR7/8 Agonist as a novel intratumoral TLR agonist for cancer therapy. A clinical trial to evaluate the safety and efficacy of TransCon TLR7/8 Agonist, as monotherapy and in combination with pembrolizumab, in cancer patients is currently ongoing (transcendIT-101; NCT04799054). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12935-022-02708-6. |
format | Online Article Text |
id | pubmed-9484246 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-94842462022-09-20 Intratumoral delivery of TransCon(™) TLR7/8 Agonist promotes sustained anti-tumor activity and local immune cell activation while minimizing systemic cytokine induction Zúñiga, Luis Alejandro Leßmann, Torben Uppal, Karan Bisek, Nicola Hong, Enping Rasmussen, Caroline E. Karlsson, Jens-Jakob Zettler, Joachim Holten-Andersen, Lars Bang, Kathy Thakar, Dhruv Lee, Yu-Chi Martinez, Salomon Sabharwal, Simran Singh Stark, Sebastian Faltinger, Frank Kracker, Oliver Weisbrod, Samuel Müller, Robin Voigt, Tobias Bigott, Kornelia Tabrizifard, Mohammad Breinholt, Vibeke Miller Mirza, Amer M. Rosen, David B. Sprogøe, Kennett Punnonen, Juha Cancer Cell Int Research BACKGROUND: Intratumoral (IT) delivery of toll-like receptor (TLR) agonists has shown encouraging anti-tumor benefit in preclinical and early clinical studies. However, IT delivery of TLR agonists may lead to rapid effusion from the tumor microenvironment (TME), potentially limiting the duration of local inflammation and increasing the risk of systemic adverse events. METHODS: To address these limitations, TransCon(™) TLR7/8 Agonist—an investigational sustained-release prodrug of resiquimod that uses a TransCon linker and hydrogel technology to achieve sustained and predictable IT release of resiquimod—was developed. TransCon TLR7/8 Agonist was characterized for resiquimod release in vitro and in vivo, in mice and rats, and was assessed for anti-tumor efficacy and pharmacodynamic activity in mice. RESULTS: Following a single IT dose, TransCon TLR7/8 Agonist mediated potent tumor growth inhibition which was associated with sustained resiquimod release over several weeks with minimal induction of systemic cytokines. TransCon TLR7/8 Agonist monotherapy promoted activation of antigen-presenting cells in the TME and tumor-draining lymph nodes, with evidence of activation and expansion of CD8(+) T cells in the tumor-draining lymph node and TME. Combination of TransCon TLR7/8 Agonist with systemic immunotherapy further promoted anti-tumor activity in TransCon TLR7/8 Agonist-treated tumors. In a bilateral tumor setting, combination of TransCon TLR7/8 Agonist with systemic IL-2 potentiated tumor growth inhibition in both injected and non-injected tumors and conferred protection against tumor rechallenge following complete regressions. CONCLUSIONS: Our findings show that a single dose of TransCon TLR7/8 Agonist can mediate sustained local release of resiquimod in the TME and promote potent anti-tumor effects as monotherapy and in combination with systemic immunotherapy, supporting TransCon TLR7/8 Agonist as a novel intratumoral TLR agonist for cancer therapy. A clinical trial to evaluate the safety and efficacy of TransCon TLR7/8 Agonist, as monotherapy and in combination with pembrolizumab, in cancer patients is currently ongoing (transcendIT-101; NCT04799054). SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12935-022-02708-6. BioMed Central 2022-09-19 /pmc/articles/PMC9484246/ /pubmed/36123697 http://dx.doi.org/10.1186/s12935-022-02708-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Zúñiga, Luis Alejandro Leßmann, Torben Uppal, Karan Bisek, Nicola Hong, Enping Rasmussen, Caroline E. Karlsson, Jens-Jakob Zettler, Joachim Holten-Andersen, Lars Bang, Kathy Thakar, Dhruv Lee, Yu-Chi Martinez, Salomon Sabharwal, Simran Singh Stark, Sebastian Faltinger, Frank Kracker, Oliver Weisbrod, Samuel Müller, Robin Voigt, Tobias Bigott, Kornelia Tabrizifard, Mohammad Breinholt, Vibeke Miller Mirza, Amer M. Rosen, David B. Sprogøe, Kennett Punnonen, Juha Intratumoral delivery of TransCon(™) TLR7/8 Agonist promotes sustained anti-tumor activity and local immune cell activation while minimizing systemic cytokine induction |
title | Intratumoral delivery of TransCon(™) TLR7/8 Agonist promotes sustained anti-tumor activity and local immune cell activation while minimizing systemic cytokine induction |
title_full | Intratumoral delivery of TransCon(™) TLR7/8 Agonist promotes sustained anti-tumor activity and local immune cell activation while minimizing systemic cytokine induction |
title_fullStr | Intratumoral delivery of TransCon(™) TLR7/8 Agonist promotes sustained anti-tumor activity and local immune cell activation while minimizing systemic cytokine induction |
title_full_unstemmed | Intratumoral delivery of TransCon(™) TLR7/8 Agonist promotes sustained anti-tumor activity and local immune cell activation while minimizing systemic cytokine induction |
title_short | Intratumoral delivery of TransCon(™) TLR7/8 Agonist promotes sustained anti-tumor activity and local immune cell activation while minimizing systemic cytokine induction |
title_sort | intratumoral delivery of transcon(™) tlr7/8 agonist promotes sustained anti-tumor activity and local immune cell activation while minimizing systemic cytokine induction |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9484246/ https://www.ncbi.nlm.nih.gov/pubmed/36123697 http://dx.doi.org/10.1186/s12935-022-02708-6 |
work_keys_str_mv | AT zunigaluisalejandro intratumoraldeliveryoftranscontlr78agonistpromotessustainedantitumoractivityandlocalimmunecellactivationwhileminimizingsystemiccytokineinduction AT leßmanntorben intratumoraldeliveryoftranscontlr78agonistpromotessustainedantitumoractivityandlocalimmunecellactivationwhileminimizingsystemiccytokineinduction AT uppalkaran intratumoraldeliveryoftranscontlr78agonistpromotessustainedantitumoractivityandlocalimmunecellactivationwhileminimizingsystemiccytokineinduction AT biseknicola intratumoraldeliveryoftranscontlr78agonistpromotessustainedantitumoractivityandlocalimmunecellactivationwhileminimizingsystemiccytokineinduction AT hongenping intratumoraldeliveryoftranscontlr78agonistpromotessustainedantitumoractivityandlocalimmunecellactivationwhileminimizingsystemiccytokineinduction AT rasmussencarolinee intratumoraldeliveryoftranscontlr78agonistpromotessustainedantitumoractivityandlocalimmunecellactivationwhileminimizingsystemiccytokineinduction AT karlssonjensjakob intratumoraldeliveryoftranscontlr78agonistpromotessustainedantitumoractivityandlocalimmunecellactivationwhileminimizingsystemiccytokineinduction AT zettlerjoachim intratumoraldeliveryoftranscontlr78agonistpromotessustainedantitumoractivityandlocalimmunecellactivationwhileminimizingsystemiccytokineinduction AT holtenandersenlars intratumoraldeliveryoftranscontlr78agonistpromotessustainedantitumoractivityandlocalimmunecellactivationwhileminimizingsystemiccytokineinduction AT bangkathy intratumoraldeliveryoftranscontlr78agonistpromotessustainedantitumoractivityandlocalimmunecellactivationwhileminimizingsystemiccytokineinduction AT thakardhruv intratumoraldeliveryoftranscontlr78agonistpromotessustainedantitumoractivityandlocalimmunecellactivationwhileminimizingsystemiccytokineinduction AT leeyuchi intratumoraldeliveryoftranscontlr78agonistpromotessustainedantitumoractivityandlocalimmunecellactivationwhileminimizingsystemiccytokineinduction AT martinezsalomon intratumoraldeliveryoftranscontlr78agonistpromotessustainedantitumoractivityandlocalimmunecellactivationwhileminimizingsystemiccytokineinduction AT sabharwalsimransingh intratumoraldeliveryoftranscontlr78agonistpromotessustainedantitumoractivityandlocalimmunecellactivationwhileminimizingsystemiccytokineinduction AT starksebastian intratumoraldeliveryoftranscontlr78agonistpromotessustainedantitumoractivityandlocalimmunecellactivationwhileminimizingsystemiccytokineinduction AT faltingerfrank intratumoraldeliveryoftranscontlr78agonistpromotessustainedantitumoractivityandlocalimmunecellactivationwhileminimizingsystemiccytokineinduction AT krackeroliver intratumoraldeliveryoftranscontlr78agonistpromotessustainedantitumoractivityandlocalimmunecellactivationwhileminimizingsystemiccytokineinduction AT weisbrodsamuel intratumoraldeliveryoftranscontlr78agonistpromotessustainedantitumoractivityandlocalimmunecellactivationwhileminimizingsystemiccytokineinduction AT mullerrobin intratumoraldeliveryoftranscontlr78agonistpromotessustainedantitumoractivityandlocalimmunecellactivationwhileminimizingsystemiccytokineinduction AT voigttobias intratumoraldeliveryoftranscontlr78agonistpromotessustainedantitumoractivityandlocalimmunecellactivationwhileminimizingsystemiccytokineinduction AT bigottkornelia intratumoraldeliveryoftranscontlr78agonistpromotessustainedantitumoractivityandlocalimmunecellactivationwhileminimizingsystemiccytokineinduction AT tabrizifardmohammad intratumoraldeliveryoftranscontlr78agonistpromotessustainedantitumoractivityandlocalimmunecellactivationwhileminimizingsystemiccytokineinduction AT breinholtvibekemiller intratumoraldeliveryoftranscontlr78agonistpromotessustainedantitumoractivityandlocalimmunecellactivationwhileminimizingsystemiccytokineinduction AT mirzaamerm intratumoraldeliveryoftranscontlr78agonistpromotessustainedantitumoractivityandlocalimmunecellactivationwhileminimizingsystemiccytokineinduction AT rosendavidb intratumoraldeliveryoftranscontlr78agonistpromotessustainedantitumoractivityandlocalimmunecellactivationwhileminimizingsystemiccytokineinduction AT sprogøekennett intratumoraldeliveryoftranscontlr78agonistpromotessustainedantitumoractivityandlocalimmunecellactivationwhileminimizingsystemiccytokineinduction AT punnonenjuha intratumoraldeliveryoftranscontlr78agonistpromotessustainedantitumoractivityandlocalimmunecellactivationwhileminimizingsystemiccytokineinduction |