Putting the sting back in STING therapy: novel delivery vehicles for improved STING activation

Engaging the immune sensing Stimulator of Interferon Genes (STING) pathway has emerged as a potentially powerful approach to cancer therapy. However, current STING agonists lack stability and specificity, resulting in toxic adverse effects and disappointing patient outcomes. Therefore, novel deliver...

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Main Authors: Sina Khorsandi, Kristin Huntoon, Jacques Lux
Format: Article
Language:English
Published: Frontiers Media S.A. 2024-04-01
Series:Frontiers in Chemical Biology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fchbi.2024.1386220/full
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author Sina Khorsandi
Kristin Huntoon
Jacques Lux
author_facet Sina Khorsandi
Kristin Huntoon
Jacques Lux
author_sort Sina Khorsandi
collection DOAJ
description Engaging the immune sensing Stimulator of Interferon Genes (STING) pathway has emerged as a potentially powerful approach to cancer therapy. However, current STING agonists lack stability and specificity, resulting in toxic adverse effects and disappointing patient outcomes. Therefore, novel delivery vehicles are needed to mitigate negative results and improve the efficacy of STING agonists. Here we discuss innovative particle-based strategies and how they have increased the therapeutic results seen with STING agonists. We review ultrasound-responsive vehicles, pH-responsive particles, inorganic particles, carriers for extended release, and particles that act as both STING agonists and/or drug carriers. Further optimization of these strategies can potentially enable the clinical use of STING agonists for cancer therapy.
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spelling doaj.art-944f43a34c904b5abb486d3aa3780dfc2024-04-05T04:43:32ZengFrontiers Media S.A.Frontiers in Chemical Biology2813-530X2024-04-01310.3389/fchbi.2024.13862201386220Putting the sting back in STING therapy: novel delivery vehicles for improved STING activationSina Khorsandi0Kristin Huntoon1Jacques Lux2Department of Radiology, University of Texas Southwestern Medical Center, Dallas, TX, United StatesDepartment of Neurosurgery, Emory University, Atlanta, GA, United StatesDepartment of Radiology, University of Texas Southwestern Medical Center, Dallas, TX, United StatesEngaging the immune sensing Stimulator of Interferon Genes (STING) pathway has emerged as a potentially powerful approach to cancer therapy. However, current STING agonists lack stability and specificity, resulting in toxic adverse effects and disappointing patient outcomes. Therefore, novel delivery vehicles are needed to mitigate negative results and improve the efficacy of STING agonists. Here we discuss innovative particle-based strategies and how they have increased the therapeutic results seen with STING agonists. We review ultrasound-responsive vehicles, pH-responsive particles, inorganic particles, carriers for extended release, and particles that act as both STING agonists and/or drug carriers. Further optimization of these strategies can potentially enable the clinical use of STING agonists for cancer therapy.https://www.frontiersin.org/articles/10.3389/fchbi.2024.1386220/fullSTINGimmunotherapycancer therapydrug deliveryparticles
spellingShingle Sina Khorsandi
Kristin Huntoon
Jacques Lux
Putting the sting back in STING therapy: novel delivery vehicles for improved STING activation
Frontiers in Chemical Biology
STING
immunotherapy
cancer therapy
drug delivery
particles
title Putting the sting back in STING therapy: novel delivery vehicles for improved STING activation
title_full Putting the sting back in STING therapy: novel delivery vehicles for improved STING activation
title_fullStr Putting the sting back in STING therapy: novel delivery vehicles for improved STING activation
title_full_unstemmed Putting the sting back in STING therapy: novel delivery vehicles for improved STING activation
title_short Putting the sting back in STING therapy: novel delivery vehicles for improved STING activation
title_sort putting the sting back in sting therapy novel delivery vehicles for improved sting activation
topic STING
immunotherapy
cancer therapy
drug delivery
particles
url https://www.frontiersin.org/articles/10.3389/fchbi.2024.1386220/full
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