An in situ depot for the sustained release of a TLR7/8 agonist in combination with a TGFβ inhibitor promotes anti-tumor immune responses

Cancer curing immune responses against heterogeneous solid cancers require that a coordinated immune activation is initiated in the antigen avid but immunosuppressive tumor microenvironment (TME). The plastic TME, and the poor systemic tolerability of immune activating drugs are, however, fundamental barriers to generating curative anticancer immune responses. Here, we introduce the CarboCell technology to overcome these barriers by forming an intratumoral sustained drug release depot that provides high payloads of immune stimulatory drugs selectively within the TME. The CarboCell thereby induces a hot spot for immune cell training and polarization and further drives and maintains the tumor-draining lymph nodes in an anticancer and immune activated state. Mechanistically, this transforms cancerous tissues, consequently generating systemic anticancer immunoreactivity. CarboCell can be injected through standard thin-needle technologies and has inherent imaging contrast which secure accurate intratumoral positioning. In particular, here we report the therapeutic performance for a dual-drug CarboCell providing sustained release of a Toll-like receptor 7/8 agonist and a transforming growth factor-β inhibitor in preclinical tumor models in female mice.

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Publication Details

Journal
Nature Communications
Published
2024-09-03
DOI
https://doi.org/10.1038/s41467-024-50967-w
Citations
8
Primary Topic
Immunotherapy and Immune Responses
Type
article
Field-Weighted Citation Impact
1.92

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article

An in situ depot for the sustained release of a TLR7/8 agonist in combination with a TGFβ inhibitor promotes anti-tumor immune responses

Camilla Stavnsbjerg, Jonas R. Henriksen, Elizabeth Serrano-Chávez, Thomas L. Andresen et al.
8 citations
Nature Communications
Immunotherapy and Immune Responses
1.92
article

An in situ depot for the sustained release of a TLR7/8 agonist in combination with a TGFβ inhibitor promotes anti-tumor immune responses

Camilla Stavnsbjerg, Jonas R. Henriksen, Elizabeth Serrano-Chávez, Thomas L. Andresen, Lars Ringgaard, Lajos Balogh, Andreas I. Jensen, Esben Christensen, Linda M. Bruun, Marouschka J. Scheeper, Fredrik Melander, Trine B. Engel, Andreas Kjær, Hólmfridur R. Halldórsdóttir, Jennifer Solgaard Jørgensen, Unnur Jóna Björgvinsdóttir, Anders E. Hansen, Martin Bak, Ditte Elisabeth Jæhger, Serhii Kostrikov, Julianna Thuróczy, Sophie B. Jensen
article en
8 citations

Abstract

Cancer curing immune responses against heterogeneous solid cancers require that a coordinated immune activation is initiated in the antigen avid but immunosuppressive tumor microenvironment (TME). The plastic TME, and the poor systemic tolerability of immune activating drugs are, however, fundamental barriers to generating curative anticancer immune responses. Here, we introduce the CarboCell technology to overcome these barriers by forming an intratumoral sustained drug release depot that provides high payloads of immune stimulatory drugs selectively within the TME. The CarboCell thereby induces a hot spot for immune cell training and polarization and further drives and maintains the tumor-draining lymph nodes in an anticancer and immune activated state. Mechanistically, this transforms cancerous tissues, consequently generating systemic anticancer immunoreactivity. CarboCell can be injected through standard thin-needle technologies and has inherent imaging contrast which secure accurate intratumoral positioning. In particular, here we report the therapeutic performance for a dual-drug CarboCell providing sustained release of a Toll-like receptor 7/8 agonist and a transforming growth factor-β inhibitor in preclinical tumor models in female mice.

Nature CommunicationsVol. 15(1)
University of Copenhagen (DK), Buda Health Center (HU), Copenhagen University Hospital (DK), Theranostics (New Zealand) (NZ), Technical University of Denmark (DK)
Lundbeckfonden, H. Lundbeck A/S
Good health and well-being
Openalex Percentile: Top 14%
Immunotherapy and Immune Responses
1.92
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