Toll-like receptor-targeted particles: A paradigm to manipulate the tumor microenvironment for cancer immunotherapy
- PMID: 31129358
- DOI: 10.1016/j.actbio.2019.05.043
Toll-like receptor-targeted particles: A paradigm to manipulate the tumor microenvironment for cancer immunotherapy
Abstract
The expression of Toll-like receptors (TLRs) on antigen presenting cells, especially dendritic cells, offers several sensitive mediators to trigger an adaptive immune response, which potentially can be exploited to detect and eliminate pathogenic objects. Consequently, numerous agonists that target TLRs are being used clinically either alone or in combination with other therapies to strengthen the immune system in the battle against cancer. This review summarizes the roles of TLRs in tumor biology, and focuses on relevant TLR-dependent antitumor pathways and the conjugation of TLR agonists as adjuvants to nano- and micro-particles for boosting responses leading to cancer suppression and eradication. STATEMENT OF SIGNIFICANCE: Toll-like receptors (TLRs), which express on antigen presenting cells, such as dendritic cells and macrophages, play an important role in sensing pathogenic agents and inducing adaptive immunity. As a result, several TLR agonists have been investigating as therapeutic agents individually or in combination with other treatment modalities for cancer treatment through boosting the immune system. This review aims to focus on the roles of TLRs in cancer and TLR-dependent antitumor pathways as well as the use of different nano- or micro-particles bearing TLR agonists for tumor inhibition and elimination.
Keywords: Biomaterials; Cancer; Immunotherapy; Particulate systems; Toll-like receptors.
Copyright © 2019 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
Similar articles
-
In vivo cancer vaccination: Which dendritic cells to target and how?Cancer Treat Rev. 2018 Dec;71:88-101. doi: 10.1016/j.ctrv.2018.10.012. Epub 2018 Oct 25. Cancer Treat Rev. 2018. PMID: 30390423 Free PMC article. Review.
-
Toll-like receptors TLR-2, TLR-4, TLR-7, and TLR-9 in tumor tissue and serum of the patients with esophageal squamous cell carcinoma and gastro-esophageal junction cancer.Adv Clin Exp Med. 2019 Apr;28(4):515-522. doi: 10.17219/acem/87012. Adv Clin Exp Med. 2019. PMID: 29968427
-
Toll-like receptors as adjuvant receptors.Biochim Biophys Acta. 2002 Feb 13;1589(1):1-13. doi: 10.1016/s0167-4889(01)00182-3. Biochim Biophys Acta. 2002. PMID: 11909637 Review.
-
The Use of Toll-Like Receptor Agonists in HIV-1 Cure Strategies.Front Immunol. 2020 Jun 11;11:1112. doi: 10.3389/fimmu.2020.01112. eCollection 2020. Front Immunol. 2020. PMID: 32595636 Free PMC article. Review.
-
TLR activation pathways in HIV-1-exposed seronegative individuals.J Immunol. 2010 Mar 1;184(5):2710-7. doi: 10.4049/jimmunol.0902463. Epub 2010 Feb 1. J Immunol. 2010. PMID: 20124101
Cited by
-
Targeting the PD-1/PD-L1 axis for cancer treatment: a review on nanotechnology.R Soc Open Sci. 2022 Apr 13;9(4):211991. doi: 10.1098/rsos.211991. eCollection 2022 Apr. R Soc Open Sci. 2022. PMID: 35425626 Free PMC article. Review.
-
Reprogramming the tumor microenvironment - macrophages emerge as key players in breast cancer immunotherapy.Front Immunol. 2024 Nov 26;15:1457491. doi: 10.3389/fimmu.2024.1457491. eCollection 2024. Front Immunol. 2024. PMID: 39660126 Free PMC article. Review.
-
Biomarker exploration of microRNA-203 as a promising substrate for predicting poor survival outcome in colorectal cancer.BMC Cancer. 2020 Oct 15;20(1):1003. doi: 10.1186/s12885-020-07512-x. BMC Cancer. 2020. PMID: 33059609 Free PMC article.
-
Applications and clinical trial landscape using Toll-like receptor agonists to reduce the toll of cancer.NPJ Precis Oncol. 2023 Mar 8;7(1):26. doi: 10.1038/s41698-023-00364-1. NPJ Precis Oncol. 2023. PMID: 36890302 Free PMC article. Review.
-
A cowpea mosaic virus adjuvant conjugated to liposomes loaded with tumor cell lysates as an ovarian cancer vaccine.Nat Commun. 2025 May 30;16(1):5047. doi: 10.1038/s41467-025-60239-w. Nat Commun. 2025. PMID: 40447608 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Research Materials
Miscellaneous