Prospects for the use of small interfering RNAs as inhibitors of immune checkpoints for immunotherapy in oncology

A. Bogdanov, V. Vysochinskaya, A. A. Kornev, A. Emelyanov, A. Bogdanov, V. Moiseyenko
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Abstract

Immune therapy is one of the most promising areas of cancer treatment. It is aimed at a cascade of processes responsible for the antitumor immune response. The involved regulatory mechanisms become targets for various therapeutic approaches aimed at restoring the impaired functions of immune cells that eliminate cancer cells. The ability of malignant cells to affect receptors of immune checkpoints is one of the most important mechanisms for suppressing antitumor immunity. The development of immune check-point inhibitors (ICIs) based on monoclonal antibodies, as well as the methods of adoptive cell therapy (ACT), are a breakthrough in the immunotherapy of malignant diseases, but it carries a number of limitations such as insufficient efficiency, safety and cost-effectiveness. The use of RNA interference technologies opens up prospects for the development of fundamentally new class of ICIs and, as a consequence, the development of more efficient ACT methods. This review presents the main problems and prospects of the use of small interfering RNA (siRNA) as the ICIs are highlighted in order to optimize modern AKT approaches
肿瘤免疫治疗中使用小干扰rna作为免疫检查点抑制剂的前景
免疫疗法是癌症治疗中最有前途的领域之一。它的目标是负责抗肿瘤免疫反应的一系列过程。所涉及的调节机制成为各种治疗方法的目标,旨在恢复免疫细胞的受损功能,从而消除癌细胞。恶性肿瘤细胞影响免疫检查点受体的能力是抑制抗肿瘤免疫的重要机制之一。基于单克隆抗体的免疫检查点抑制剂(ICIs)和过继细胞治疗(ACT)方法的发展是恶性疾病免疫治疗的突破,但存在效率、安全性和成本效益不足等局限性。RNA干扰技术的使用为开发全新类型的ici开辟了前景,并因此开发了更有效的ACT方法。本文综述了利用小干扰RNA (siRNA)作为ICIs的主要问题和前景,以优化现代AKT方法
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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