RNF43 p.G659fs 通过 PI3K/AKT/mTOR 信号通路和 HLA-E 上调导致 MSI-high 结直肠癌中 NK 细胞功能障碍
RNF43 p.G659fs leads to natural killer cell dysfunction in MSI-high colorectal cancer through PI3K/AKT/mTOR signaling and HLA-E up-regulation.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Dendritic cell‑based vaccines for colorectal cancer: Mechanisms, clinical progress and future directions (Review).
Dendritic cell‑based vaccines for colorectal cancer: Mechanisms, clinical progress and future directions (Review).
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
基于树突状细胞(DC)的疫苗已成为一种有前景的免疫疗法,可用于对抗多种癌症。DC是哨兵抗原呈递细胞,通过先天免疫反应识别肿瘤抗原,随后刺激适应性T细胞介导的抗肿瘤反应,在癌症免疫监视中发挥关键作用。自体DC疫苗激发个体免疫系统识别并摧毁肿瘤细胞,旨在实现持久的抗肿瘤免疫并阻止肿瘤复发。DC疫苗用于癌症治疗的安全性和有效性已在多项临床研究中得到证实,无论是作为单一疗法(如Sipuleucel-T)还是与化疗和免疫检查点阻断等其他疗法联合使用。本综述全面概述了DC疫苗用于结直肠癌(CRC)的当前进展和临床应用。详细探讨了DC的各种亚群及其在抗肿瘤免疫中的生物学作用,并讨论了DC疫苗开发的机制见解。
此外,本综述重点介绍了近期自体DC疫苗用于晚期CRC临床试验的结果,以及在CRC开发和临床应用中所面临的挑战和克服策略。
总之,本综述强调了DC疫苗用于CRC的潜力和局限性,以提供更好的理解并指导未来开发有效的DC治疗性疫苗用于CRC的方向。
Dendritic cell (DC)‑based vaccines have emerged as a promising immunotherapy against a broad range of cancers. DCs are sentinel antigen‑presenting cells that play a pivotal role in cancer immunosurveillance by recognizing tumor antigens via innate immune responses and subsequently stimulating adaptive T‑cell‑mediated anti‑tumor responses. Autologous DC‑based vaccines prime the individual's immune system to recognize and destroy tumor cells, aiming to achieve durable anti‑tumor immunity and impede tumor relapse.
The safety and effectiveness of DC‑based vaccines for cancer treatment have been demonstrated in several clinical studies, either as monotherapy (such as Sipuleucel‑T) or in combination with other therapies such as chemotherapy and immune checkpoint blockade.
The present review provides a comprehensive overview of the current progress and clinical applications of DC‑based vaccines for colorectal cancer (CRC). Various subsets of DCs and their biological roles in anti‑tumor immunity are explored in detail and the mechanistic insights into DC‑based vaccine development are discussed.
Additionally, the present review highlighted the outcomes of recent clinical trials of autologous DC‑based vaccines for advanced CRC, as well as the challenges and strategies for overcoming them in the development and clinical applications for CRC. Taken together, the potential and limitations of DC‑based vaccines for CRC are underscored in the present review to provide an improved understanding and guide future directions in developing efficacious DC‑based therapeutic vaccines for CRC.
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