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:Tumor immunology: unraveling the complex interaction between tumors and the immune system: a narrative review.
Tumor immunology: unraveling the complex interaction between tumors and the immune system: a narrative review.
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肿瘤免疫学是癌症研究的一个关键领域,主要关注免疫系统与肿瘤细胞之间的相互作用。免疫系统能够通过多种免疫细胞,如细胞毒性T淋巴细胞(CTLs)和自然杀伤(NK)细胞,识别并清除癌细胞。然而,肿瘤已经发展出复杂的机制来逃避免疫检测,例如肿瘤抗原表达的缺失、免疫抑制细胞的募集以及免疫检查点的上调。这些免疫逃逸策略使肿瘤能够不受控制地生长和转移。免疫疗法已成为一种有前景的治疗方式,利用免疫系统的力量来对抗癌症。关键策略包括免疫检查点抑制剂,其阻断抑制性受体如程序性细胞死亡蛋白1和细胞毒性T淋巴细胞相关蛋白4,以及过继性细胞疗法,其涉及将肿瘤特异性T细胞或NK细胞转移到患者体内。此外,单克隆抗体和癌症疫苗正在被探索用于直接靶向肿瘤细胞并增强免疫反应。尽管这些疗法取得了成功,但肿瘤异质性、治疗耐药性和免疫相关不良反应等挑战仍然存在。
Tumor immunology is a critical area of cancer research that focuses on the interplay between the immune system and tumor cells. The immune system has the ability to recognize and eliminate cancer cells through various immune cells, such as cytotoxic T lymphocytes (CTLs) and natural killer (NK) cells.
However, tumors have developed sophisticated mechanisms to evade immune detection, such as the loss of tumor antigen expression, recruitment of immunosuppressive cells, and upregulation of immune checkpoints. These immune evasion strategies allow tumors to grow uncontrollably and metastasize.
Immunotherapy has emerged as a promising treatment modality that harnesses the power of the immune system to fight cancer. Key strategies include immune checkpoint inhibitors, which block inhibitory receptors like programmed cell death protein 1 and cytotoxic T-lymphocyte-associated protein 4, and adoptive cell therapies, which involve the transfer of tumor-specific T cells or NK cells into patients.
Additionally, monoclonal antibodies and cancer vaccines are being explored to directly target tumor cells and enhance immune responses. Despite the success of these therapies, challenges such as tumor heterogeneity, resistance to treatment, and immune-related adverse effects persist.
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