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:The emerging field of oncolytic virus-based cancer immunotherapy.
The emerging field of oncolytic virus-based cancer immunotherapy.
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溶瘤病毒(OVs)为对传统疗法耐药的癌症患者提供了新颖且有前景的治疗选择。天然或基因修饰的OVs是多方面的肿瘤杀手。它们直接裂解肿瘤细胞而不伤害正常细胞,并通过释放抗原和激活肿瘤微环境中的炎症反应间接增强抗肿瘤免疫。然而,一些局限性,如OVs对肿瘤的渗透有限、持续时间短以及宿主抗病毒免疫反应,正在阻碍溶瘤病毒疗法广泛转化为临床应用。如果这些挑战能够被克服,联合疗法,如OVs加免疫检查点阻断(ICB)、嵌合抗原受体(CAR)T细胞或CAR自然杀伤(NK)细胞,可能在临床上提供强大的治疗平台。
Oncolytic viruses (OVs) provide novel and promising therapeutic options for patients with cancers resistant to traditional therapies. Natural or genetically modified OVs are multifaceted tumor killers. They directly lyse tumor cells while sparing normal cells, and indirectly potentiate antitumor immunity by releasing antigens and activating inflammatory responses in the tumor microenvironment.
However, some limitations, such as limited penetration of OVs into tumors, short persistence, and the host antiviral immune response, are impeding the broad translation of oncolytic virotherapy into the clinic. If these challenges can be overcome, combination therapies, such as OVs plus immune checkpoint blockade (ICB), chimeric antigen receptor (CAR) T cells, or CAR natural killer (NK) cells, may provide powerful therapeutic platforms in the clinic.
在 PubMed 查看 → 出版商原文(DOI) 全文 PDF(PMC)· 可下载 治疗专题与资料阅读指南 资料来源与翻译说明 报告译文或资料问题 →
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