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An in situ hydrogel-mediated chemo-immunometabolic cancer therapy

Metabolic reprogramming of the tumor microenvironment (TME) and poor immunogenicity are two of the challenges that cancer immunotherapies have to overcome for improved clinical benefits. Among various immunosuppressive metabolites that keep anti-tumor immunity in check, the tryptophan catabolite kyn...

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Autores principales: Wang, Bo, Chen, Jing, Caserto, Julia S., Wang, Xi, Ma, Minglin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9250515/
https://www.ncbi.nlm.nih.gov/pubmed/35780226
http://dx.doi.org/10.1038/s41467-022-31579-8
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author Wang, Bo
Chen, Jing
Caserto, Julia S.
Wang, Xi
Ma, Minglin
author_facet Wang, Bo
Chen, Jing
Caserto, Julia S.
Wang, Xi
Ma, Minglin
author_sort Wang, Bo
collection PubMed
description Metabolic reprogramming of the tumor microenvironment (TME) and poor immunogenicity are two of the challenges that cancer immunotherapies have to overcome for improved clinical benefits. Among various immunosuppressive metabolites that keep anti-tumor immunity in check, the tryptophan catabolite kynurenine (Kyn) is an attractive target for blockade given its role in mediating immunosuppression through multiple pathways. Here, we present a local chemo-immunometabolic therapy through injection of a supramolecular hydrogel concurrently releasing doxorubicin that induces immunogenic tumor cell death and kynureninase that disrupts Kyn-mediated immunosuppressive pathways in TME. The combination synergically enhances tumor immunogenicity and unleashes anti-tumor immunity. In mouse models of triple negative breast cancer and melanoma, a single low dose peritumoral injection of the therapeutic hydrogel promotes TME transformation toward more immunostimulatory, which leads to enhanced tumor suppression and extended mouse survival. In addition, the systemic anti-tumor surveillance induced by the local treatment exhibits an abscopal effect and prevents tumor relapse post-resection. This versatile approach for local chemo-immunometabolic therapy may serve as a general strategy for enhancing anti-tumor immunity and boosting the efficacy of cancer immunotherapies.
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spelling pubmed-92505152022-07-04 An in situ hydrogel-mediated chemo-immunometabolic cancer therapy Wang, Bo Chen, Jing Caserto, Julia S. Wang, Xi Ma, Minglin Nat Commun Article Metabolic reprogramming of the tumor microenvironment (TME) and poor immunogenicity are two of the challenges that cancer immunotherapies have to overcome for improved clinical benefits. Among various immunosuppressive metabolites that keep anti-tumor immunity in check, the tryptophan catabolite kynurenine (Kyn) is an attractive target for blockade given its role in mediating immunosuppression through multiple pathways. Here, we present a local chemo-immunometabolic therapy through injection of a supramolecular hydrogel concurrently releasing doxorubicin that induces immunogenic tumor cell death and kynureninase that disrupts Kyn-mediated immunosuppressive pathways in TME. The combination synergically enhances tumor immunogenicity and unleashes anti-tumor immunity. In mouse models of triple negative breast cancer and melanoma, a single low dose peritumoral injection of the therapeutic hydrogel promotes TME transformation toward more immunostimulatory, which leads to enhanced tumor suppression and extended mouse survival. In addition, the systemic anti-tumor surveillance induced by the local treatment exhibits an abscopal effect and prevents tumor relapse post-resection. This versatile approach for local chemo-immunometabolic therapy may serve as a general strategy for enhancing anti-tumor immunity and boosting the efficacy of cancer immunotherapies. Nature Publishing Group UK 2022-07-02 /pmc/articles/PMC9250515/ /pubmed/35780226 http://dx.doi.org/10.1038/s41467-022-31579-8 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Wang, Bo
Chen, Jing
Caserto, Julia S.
Wang, Xi
Ma, Minglin
An in situ hydrogel-mediated chemo-immunometabolic cancer therapy
title An in situ hydrogel-mediated chemo-immunometabolic cancer therapy
title_full An in situ hydrogel-mediated chemo-immunometabolic cancer therapy
title_fullStr An in situ hydrogel-mediated chemo-immunometabolic cancer therapy
title_full_unstemmed An in situ hydrogel-mediated chemo-immunometabolic cancer therapy
title_short An in situ hydrogel-mediated chemo-immunometabolic cancer therapy
title_sort in situ hydrogel-mediated chemo-immunometabolic cancer therapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9250515/
https://www.ncbi.nlm.nih.gov/pubmed/35780226
http://dx.doi.org/10.1038/s41467-022-31579-8
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