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:Engaging natural killer cells for cancer therapy via NKG2D, CD16A and other receptors.
Engaging natural killer cells for cancer therapy via NKG2D, CD16A and other receptors.
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免疫肿瘤学改变了癌症患者照护方式,改善了患者生存和生活质量。该领域的大部分研究聚焦于通过靶向T细胞来发挥适应性免疫应答的作用。尽管这类方法推动了领域进展,但仍存在挑战,且T细胞疗法并非对所有患者或肿瘤类型都有效。因此,激活先天免疫系统等替代策略已成为研究重点。尤其是利用自然杀伤(NK)细胞作为强效先天免疫效应细胞,已成为一种有前景的免疫治疗方式。本文综述选择性激活NK细胞以治疗癌症的策略,重点介绍靶向关键活化受体NK细胞受体2D(NKG2D)和分化簇16A(CD16A)的方法。
The field of immuno-oncology has revolutionized cancer patient care and improved survival and quality of life for patients. Much of the focus in the field has been on exploiting the power of the adaptive immune response through therapeutic targeting of T cells. While these approaches have markedly advanced the field, some challenges remain, and the clinical benefit of T cell therapies does not extend to all patients or tumor indications.
Alternative strategies, such as engaging the innate immune system, have become an intense area of focus in the field. In particular, the engagement of natural killer (NK) cells as potent effectors of the innate immune response has emerged as a promising modality in immunotherapy.
Here, we review therapeutic approaches for selective engagement of NK cells for cancer therapy, with a particular focus on targeting the key activating receptors NK Group 2D (NKG2D) and cluster of differentiation 16A (CD16A).
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