STING疗法中的 "刺痛":改善STING激活的新型传输载体

Sina Khorsandi, Kristin Huntoon, Jacques Lux
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引用次数: 0

摘要

利用免疫感应干扰素基因刺激器(STING)通路已成为一种潜在的强大癌症治疗方法。然而,目前的 STING 激动剂缺乏稳定性和特异性,导致毒性不良反应和令人失望的患者疗效。因此,需要新颖的给药载体来减轻不良反应,提高 STING 激动剂的疗效。在此,我们将讨论基于微粒的创新策略,以及这些策略如何提高 STING 激动剂的治疗效果。我们回顾了超声响应载体、pH 值响应微粒、无机微粒、缓释载体以及同时作为 STING 激动剂和/或药物载体的微粒。这些策略的进一步优化有可能使 STING 激动剂用于癌症治疗的临床应用成为可能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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 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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