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Trial watch: TLR3 agonists in cancer therapy.

Authors :
Le Naour, Julie
Galluzzi, Lorenzo
Zitvogel, Laurence
Kroemer, Guido
Vacchelli, Erika
Source :
OncoImmunology. 2020, Vol. 9 Issue 1, p1-11. 11p.
Publication Year :
2020

Abstract

Toll-like receptor 3 (TLR3) is a pattern recognition receptor that senses exogenous (viral) as well as endogenous (mammalian) double-stranded RNA in endosomes. On activation, TLR3 initiates a signal transduction pathway that culminates with the secretion of pro-inflammatory cytokines including type I interferon (IFN). The latter is essential not only for innate immune responses to infection but also for the initiation of antigen-specific immunity against viruses and malignant cells. These aspects of TLR3 biology have supported the development of various agonists for use as stand-alone agents or combined with other therapeutic modalities in cancer patients. Here, we review recent preclinical and clinical advances in the development of TLR3 agonists for oncological disorders. cDC, conventional dendritic cell; CMT, cytokine modulating treatment; CRC, colorectal carcinoma; CTL, cytotoxic T lymphocyte; DC, dendritic cell; dsRNA, double-stranded RNA; FLT3LG, fms-related receptor tyrosine kinase 3 ligand; HNSCC, head and neck squamous cell carcinoma; IFN, interferon; IL, interleukin; ISV, in situ vaccine; MUC1, mucin 1, cell surface associated; PD-1, programmed cell death 1; PD-L1, programmed death-ligand 1; polyA:U, polyadenylic:polyuridylic acid; polyI:C, polyriboinosinic:polyribocytidylic acid; TLR, Toll-like receptor [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
21624011
Volume :
9
Issue :
1
Database :
Academic Search Index
Journal :
OncoImmunology
Publication Type :
Academic Journal
Accession number :
147926198
Full Text :
https://doi.org/10.1080/2162402X.2020.1771143