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Immunostimulatory nanomedicines synergize with checkpoint blockade immunotherapy to eradicate colorectal tumors
Nanoparticles can potentially stimulate tumour microenvironments to elicit antitumour immunity. Herein, we demonstrate effective immunotherapy of colorectal cancer via systemic delivery of an immunostimulatory chemotherapeutic combination in nanoscale coordination polymer (NCP) core-shell particles....
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6478897/ https://www.ncbi.nlm.nih.gov/pubmed/31015397 http://dx.doi.org/10.1038/s41467-019-09221-x |
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author | Duan, Xiaopin Chan, Christina Han, Wenbo Guo, Nining Weichselbaum, Ralph R. Lin, Wenbin |
author_facet | Duan, Xiaopin Chan, Christina Han, Wenbo Guo, Nining Weichselbaum, Ralph R. Lin, Wenbin |
author_sort | Duan, Xiaopin |
collection | PubMed |
description | Nanoparticles can potentially stimulate tumour microenvironments to elicit antitumour immunity. Herein, we demonstrate effective immunotherapy of colorectal cancer via systemic delivery of an immunostimulatory chemotherapeutic combination in nanoscale coordination polymer (NCP) core-shell particles. Oxaliplatin and dihydroartemesinin have contrasting physicochemical properties but strong synergy in reactive oxygen species (ROS) generation and anticancer activity. The combined ROS generation is harnessed for immune activation to synergize with an anti-PD-L1 antibody for the treatment of murine colorectal cancer tumours. The favourable biodistribution and tumour uptake of NCPs and the absence of peripheral neuropathy allow for repeated dosing to afford 100% tumour eradication. The involvement of innate and adaptive immune systems elicit strong and long lasting antitumour immunity which prevents tumour formation when cured mice are challenged with cancer cells. The intrinsically biodegradable, well tolerated, and systemically available immunostimulatory NCP promises to enter clinical testing as an immunotherapy against colorectal cancer. |
format | Online Article Text |
id | pubmed-6478897 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64788972019-04-25 Immunostimulatory nanomedicines synergize with checkpoint blockade immunotherapy to eradicate colorectal tumors Duan, Xiaopin Chan, Christina Han, Wenbo Guo, Nining Weichselbaum, Ralph R. Lin, Wenbin Nat Commun Article Nanoparticles can potentially stimulate tumour microenvironments to elicit antitumour immunity. Herein, we demonstrate effective immunotherapy of colorectal cancer via systemic delivery of an immunostimulatory chemotherapeutic combination in nanoscale coordination polymer (NCP) core-shell particles. Oxaliplatin and dihydroartemesinin have contrasting physicochemical properties but strong synergy in reactive oxygen species (ROS) generation and anticancer activity. The combined ROS generation is harnessed for immune activation to synergize with an anti-PD-L1 antibody for the treatment of murine colorectal cancer tumours. The favourable biodistribution and tumour uptake of NCPs and the absence of peripheral neuropathy allow for repeated dosing to afford 100% tumour eradication. The involvement of innate and adaptive immune systems elicit strong and long lasting antitumour immunity which prevents tumour formation when cured mice are challenged with cancer cells. The intrinsically biodegradable, well tolerated, and systemically available immunostimulatory NCP promises to enter clinical testing as an immunotherapy against colorectal cancer. Nature Publishing Group UK 2019-04-23 /pmc/articles/PMC6478897/ /pubmed/31015397 http://dx.doi.org/10.1038/s41467-019-09221-x Text en © The Author(s) 2019 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/. |
spellingShingle | Article Duan, Xiaopin Chan, Christina Han, Wenbo Guo, Nining Weichselbaum, Ralph R. Lin, Wenbin Immunostimulatory nanomedicines synergize with checkpoint blockade immunotherapy to eradicate colorectal tumors |
title | Immunostimulatory nanomedicines synergize with checkpoint blockade immunotherapy to eradicate colorectal tumors |
title_full | Immunostimulatory nanomedicines synergize with checkpoint blockade immunotherapy to eradicate colorectal tumors |
title_fullStr | Immunostimulatory nanomedicines synergize with checkpoint blockade immunotherapy to eradicate colorectal tumors |
title_full_unstemmed | Immunostimulatory nanomedicines synergize with checkpoint blockade immunotherapy to eradicate colorectal tumors |
title_short | Immunostimulatory nanomedicines synergize with checkpoint blockade immunotherapy to eradicate colorectal tumors |
title_sort | immunostimulatory nanomedicines synergize with checkpoint blockade immunotherapy to eradicate colorectal tumors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6478897/ https://www.ncbi.nlm.nih.gov/pubmed/31015397 http://dx.doi.org/10.1038/s41467-019-09221-x |
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