Therapeutic mRNAs for cancer immunotherapy: From structure to delivery.

3区 医学 Q2 Medicine
Advances in Immunology Pub Date : 2025-01-01 Epub Date: 2024-12-03 DOI:10.1016/bs.ai.2024.10.013
Monika Vishwakarma, Wasim Akram, Tanweer Haider
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引用次数: 0

Abstract

mRNA carries genetic information and is used for the synthesis of proteins, fragments of proteins, and peptides in the scope of biotechnology and medicine. Once introduced into cells, this mRNA gets translated into a corresponding protein with cellular machinery. All kinds of mRNA encoding any protein, peptide, and fragment of proteins have been designed to be used for various therapeutic goals, including cancerous diseases, immunotherapy, vaccine preparation, tissue engineering, and genetic disorders, among others. These vaccines encode tumor-specific antigens that stimulate the immune system to recognize and attack cancer cells. Additionally, mRNA can be designed to produce proteins that modulate immune checkpoints, thereby enhancing the immune system's ability to target cancer cells. Synthetic mRNA can also engineer immune cells, such as T cells, to improve their cancer-fighting capabilities. For instance, mRNA can be engineered to generate CAR T cells targeting specific antigens that are expressed in the cancer. Designed mRNA can encode functional proteins in patients suffering from genetic disorders characterized by an absence or defect in a particular protein. However, mRNA is intrinsically unstable and may require special mechanisms to protect it from degradation. mRNA delivery to target cells remains a challenge. Engineered nanocarriers containing mRNA can improve the efficiency and enable the delivery to specific sites, that can provide a stimulant or substance for therapeutic purposes. This combination may improve their stability and efficacy in multiple applications of therapies. The following chapter throws light on basic advances in mRNA-based cancer therapy and provides insights into the nanotherapeutics using mRNA in key preclinical developments and the evolving clinical landscape.

癌症免疫治疗的治疗性mrna:从结构到递送。
mRNA携带遗传信息,在生物技术和医学领域用于蛋白质、蛋白质片段和肽的合成。一旦被引入细胞,这种mRNA就会通过细胞机制被翻译成相应的蛋白质。编码任何蛋白质、肽和蛋白质片段的各种mRNA已被设计用于各种治疗目的,包括癌症疾病、免疫治疗、疫苗制备、组织工程和遗传疾病等。这些疫苗编码肿瘤特异性抗原,刺激免疫系统识别和攻击癌细胞。此外,mRNA可以被设计成产生调节免疫检查点的蛋白质,从而增强免疫系统靶向癌细胞的能力。合成mRNA还可以改造免疫细胞,如T细胞,以提高它们的抗癌能力。例如,mRNA可以被改造成产生CAR - T细胞,靶向在癌症中表达的特定抗原。设计的mRNA可以在患有以特定蛋白质缺失或缺陷为特征的遗传疾病的患者中编码功能蛋白。然而,mRNA本质上是不稳定的,可能需要特殊的机制来保护它免受降解。mRNA递送到靶细胞仍然是一个挑战。含有mRNA的工程化纳米载体可以提高效率并使其能够递送到特定的位点,从而可以提供用于治疗目的的兴奋剂或物质。这种组合可以提高它们在多种治疗应用中的稳定性和疗效。下一章介绍了基于mRNA的癌症治疗的基本进展,并提供了在关键的临床前发展和不断发展的临床前景中使用mRNA的纳米治疗的见解。
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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来源期刊
Advances in Immunology
Advances in Immunology 医学-免疫学
CiteScore
9.90
自引率
0.00%
发文量
13
期刊介绍: Advances in Immunology has provided students and researchers with the latest information in Immunology for over 50 years. You can continue to rely on Advances in Immunology to provide you with critical reviews that examine subjects of vital importance to the field through summary and evaluation of current knowledge and research. The articles stress fundamental concepts, but also evaluate the experimental approaches.
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