调节性 T 细胞 (Treg) 在肿瘤发生中的作用:全面文献综述

Kian Torabiardakani
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摘要

简介调节性 T 细胞(Tregs)是 CD4+ T 淋巴细胞的一个亚群,它通过抑制过度的免疫激活来促进免疫平衡。然而,这些免疫抑制特性会导致抗肿瘤免疫反应受到抑制。通过疗法消耗或阻断Tregs已成为增强抗肿瘤免疫力的一种可能方法。然而,缺乏对肿瘤微环境中 Tregs 的选择性靶向是 Treg 疗法有效性的一大限制。因此,本研究旨在回顾目前有关 Tregs 如何抑制抗肿瘤免疫反应以及如何靶向 Tregs 促进抗肿瘤免疫的文献。方法:本综述研究了肿瘤微环境中 Tregs 的最新文献,重点关注细胞接触依赖机制和独立机制。此外还包括临床试验研究,以评估Tregs的治疗靶点。本文在PubMed数据库中系统检索了2010年至今的英文文章,并辅以无日期限制的人工检索。布尔表达确保了研究检索的全面性。结果Tregs参与多种癌症类型的发展是显而易见的,以这些细胞为靶点有可能提高抗肿瘤免疫的效果。此外,我们还汇编了一份目前用于癌症Treg靶向的新方法清单。讨论:本综述为基于 Treg 的疗法确定了最有前景的靶点,为加速开发创新癌症疗法开辟了道路。结论我们的文献综述让我们深入了解了免疫系统与癌症之间复杂的相互作用。对这种相互作用的理解不仅仅是一个终点,还有可能成为新科学发现的垫脚石。
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The Role of Regulatory T cells (Tregs) in Tumorigenesis: A Comprehensive Literature Review
Introduction: Regulatory T cells (Tregs) are a subpopulation of CD4+ T lymphocytes that contribute to immune homeostasis by suppressing excessive immune activation. However, these immunosuppressive properties can lead to the suppression of anti-tumor immune responses. Depletion or blocking of Tregs through therapeutics has emerged as a possible method for enhancing anti-tumor immunity. However, the lack of selective targeting of Tregs in the tumor microenvironment is a significant limitation to the effectiveness of Treg therapies. Therefore, this investigation aims to review current literature on how Tregs suppress the antitumor immune response and how they can be targeted to promote anti-tumor immunity. Methods: This review examines recent literature on Tregs in the tumor microenvironment, focusing on both cell-contact dependent and independent mechanisms. Clinical trial studies were also included to assess therapeutic targeting of Tregs. The PubMed database was systematically searched for English articles from 2010 to present, supplemented by manual searches without date restrictions. Boolean expressions ensured comprehensive study retrieval. Results: The involvement of Tregs in the development of multiple cancer types is evident, and targeting these cells could potentially enhance the efficacy of antitumor immunity. In addition, we compiled a list of the novel approaches currently being used for Treg targeting in the context of cancer. Discussion: This review has identified the most promising targets for Treg-based therapies, opening avenues for accelerating the development of innovative cancer treatments. Conclusion: Our literature review offers insights into the complex interplay between the immune system and cancer. The understanding of this interaction is not just an endpoint but could potentially act as a steppingstone towards new scientific discoveries.
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