Yangjie Liu, Cao Peng, Faiza Ahad, Syed Aqib Ali Zaidi, Tobias Achu Muluh, Qiuxia Fu
{"title":"Advanced Strategies of CAR-T Cell Therapy in Solid Tumors and Hematological Malignancies.","authors":"Yangjie Liu, Cao Peng, Faiza Ahad, Syed Aqib Ali Zaidi, Tobias Achu Muluh, Qiuxia Fu","doi":"10.2174/0115748928277331231218115402","DOIUrl":null,"url":null,"abstract":"<p><p>Chimeric antigen receptor T-cells, known as CAR-T cells, represent a promising breakthrough in the realm of adoptive cell therapy. These T-cells are genetically engineered to carry chimeric antigen receptors that specifically target tumors. They have achieved notable success in the treatment of blood-related cancers, breathing new life into this field of medical research. However, numerous obstacles limit chimeric antigen receptors T-cell therapy's efficacy, such as it cannot survive in the body long. It is prone to fatigue and exhaustion, leading to difficult tumor elimination and repeated recurrence, affecting solid tumors and hematological malignancies. The challenges posed by solid tumors, especially in the context of the complex solid-tumor microenvironment, require specific strategies. This review outlines recent advancements in improving chimeric antigen receptors T-cell therapy by focusing on the chimeric antigen receptors protein, modifying T-cells, and optimizing the interaction between T-cells and other components within the tumor microenvironment. This article aims to provide an extensive summary of the latest discoveries regarding CAR-T cell therapy, encompassing its application across various types of human cancers. Moreover, it will delve into the obstacles that have emerged in recent times, offering insights into the challenges faced by this innovative approach. Finally, it highlights novel therapeutic options in treating hematological and solid malignancies with chimeric antigen receptors T-cell therapies.</p>","PeriodicalId":94186,"journal":{"name":"Recent patents on anti-cancer drug discovery","volume":" ","pages":"557-572"},"PeriodicalIF":0.0000,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Recent patents on anti-cancer drug discovery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/0115748928277331231218115402","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Chimeric antigen receptor T-cells, known as CAR-T cells, represent a promising breakthrough in the realm of adoptive cell therapy. These T-cells are genetically engineered to carry chimeric antigen receptors that specifically target tumors. They have achieved notable success in the treatment of blood-related cancers, breathing new life into this field of medical research. However, numerous obstacles limit chimeric antigen receptors T-cell therapy's efficacy, such as it cannot survive in the body long. It is prone to fatigue and exhaustion, leading to difficult tumor elimination and repeated recurrence, affecting solid tumors and hematological malignancies. The challenges posed by solid tumors, especially in the context of the complex solid-tumor microenvironment, require specific strategies. This review outlines recent advancements in improving chimeric antigen receptors T-cell therapy by focusing on the chimeric antigen receptors protein, modifying T-cells, and optimizing the interaction between T-cells and other components within the tumor microenvironment. This article aims to provide an extensive summary of the latest discoveries regarding CAR-T cell therapy, encompassing its application across various types of human cancers. Moreover, it will delve into the obstacles that have emerged in recent times, offering insights into the challenges faced by this innovative approach. Finally, it highlights novel therapeutic options in treating hematological and solid malignancies with chimeric antigen receptors T-cell therapies.
嵌合抗原受体T细胞(又称CAR-T细胞)是采用性细胞疗法领域一个很有希望的突破。这些 T 细胞经过基因工程改造,携带有专门针对肿瘤的嵌合抗原受体。它们在治疗血液相关癌症方面取得了显著成功,为这一医学研究领域注入了新的活力。然而,许多障碍限制了嵌合抗原受体 T 细胞疗法的疗效,例如它无法在体内长期存活。它容易产生疲劳和衰竭,导致肿瘤难以消除和反复复发,影响实体瘤和血液恶性肿瘤。实体瘤带来的挑战,尤其是在复杂的实体瘤微环境背景下,需要特定的策略。这篇综述概述了通过关注嵌合抗原受体蛋白、改造 T 细胞以及优化 T 细胞与肿瘤微环境中其他成分之间的相互作用来改进嵌合抗原受体 T 细胞疗法的最新进展。本文旨在广泛总结有关 CAR-T 细胞疗法的最新发现,包括其在各类人类癌症中的应用。此外,文章还将深入探讨近来出现的障碍,深入分析这种创新方法所面临的挑战。最后,它将重点介绍利用嵌合抗原受体 T 细胞疗法治疗血液和实体恶性肿瘤的新型治疗方案。