| Literature DB >> 32449776 |
Michael P Plebanek, Michael Sturdivant, Nicholas C DeVito, Brent A Hanks.
Abstract
The dendritic cell (DC) is recognized as a vital mediator of anti-tumor immunity. More recent studies have also demonstrated the important role of DCs in the generation of effective responses to checkpoint inhibitor immunotherapy. Metabolic programming of DCs dictates their functionality and can determine which DCs become immunostimulatory versus those that develop a tolerized phenotype capable of actively suppressing effector T-cell responses to cancers. As a result, there is great interest in understanding what mechanisms have evolved in cancers to alter these metabolic pathways, thereby allowing for their continued progression and metastasis. The therapeutic strategies developed to reverse these processes of DC tolerization in the tumor microenvironment represent promising candidates for future testing in combination immunotherapy clinical trials. © The Japanese Society for Immunology. 2020. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.Entities:
Keywords: 3-dioxygenase; PPAR; fatty acid oxidation; indoleamine 2; lipid bodies; β-catenin
Mesh:
Year: 2020 PMID: 32449776 PMCID: PMC7318778 DOI: 10.1093/intimm/dxaa036
Source DB: PubMed Journal: Int Immunol ISSN: 0953-8178 Impact factor: 4.823