多形性胶质母细胞瘤对免疫系统的规避:实现有效治疗的障碍

Kevin Johanes Kawengian, S. Wanandi
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摘要

多形性胶质母细胞瘤(GBM)是一种侵袭性极强的恶性脑癌,一直是肿瘤学领域的重大挑战。尽管治疗策略在不断进步,但 GBM 患者的预后仍然不容乐观,5 年生存率徘徊在 5%左右。GBM 的治疗涉及多种治疗方法,包括免疫疗法,但在克服肿瘤复发和耐药性方面尚未取得最佳治疗效果。导致 GBM 耐药性和病情进展的一个关键因素是肿瘤逃避免疫系统的能力,即所谓的癌症免疫逃逸。这一现象反映了肿瘤细胞为适应和在机体免疫反应中存活所做的努力。GBM 细胞释放和表达的 TGF-ß、IL-10、PD-L1 和 NKG2DL 等分子会影响免疫系统对肿瘤细胞的激活、识别和清除。此外,MDSCs、Tregs 和 TAMs 等细胞的参与也会抑制免疫系统的功能,从而促进 GBM 细胞的发展。在技术进步的支持下,更好地理解 GBM 的免疫逃逸将大大有助于未来对 GBM 患者的治疗管理。 关键词:多形性胶质母细胞瘤;GBM;癌症免疫;免疫逃避;免疫逃逸;免疫疗法
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evasion of the Immune System by Glioblastoma Multiforme: An Obstacle to Achieving Effective Therapies
Glioblastoma multiforme (GBM), a highly aggressive and malignant form of brain cancer, continues to pose a significant challenge in the field of oncology. Despite ongoing advancements in treatment strategies, the prognosis for GBM patients remains grim, with a 5-year survival rate hovering around 5%. The management of GBM involves multiple therapeutic approaches, including immunotherapy, but optimal treatment outcomes in terms of overcoming tumor recurrence and resistance have not been achieved. A key factor contributing to therapy resistance and the progression of GBM is the tumor's ability to evade the immune system, referred to as immune escape from cancer. This phenomenon reflects the tumor cells' efforts to adapt and survive the body's immune response. The release and expression of molecules like TGF-ß, IL-10, PD-L1, and NKG2DL by GBM cells impact the activation, recognition, and elimination of tumor cells by the immune system. Additionally, the involvement of cells such as MDSCs, Tregs, and TAMs plays a role in inhibiting the immune system's function, thereby promoting the development of GBM cells. A better comprehension of GBM's immune escape, supported by technological advances, will significantly aid in the future management of GBM patients' treatment.Keywords: glioblastoma multiforme, GBM, cancer immunity, immune evasion, immune escape, immunotherapy
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