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:First-in-human evaluation of memory-like NK cells with an IL-15 super-agonist and CTLA-4 blockade in advanced head and neck cancer.
First-in-human evaluation of memory-like NK cells with an IL-15 super-agonist and CTLA-4 blockade in advanced head and neck cancer.
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CIML NK 细胞联合 N-803 和 ipilimumab 治疗头颈癌是安全的,并与更具增殖性的 NK 细胞表型相关。然而,该联合方案导致 HLA 错配 NK 细胞持久性降低,从而成为影响临床试验中 NK 细胞联合疗法的一个重要局限性。这些结果为 CIML NK 疗法用于晚期恶性肿瘤的评估提供了依据,并需考虑与 IPI 的联合应用。
细胞因子诱导的记忆样NK 细胞(CIML NK)联合 IL-15 超级激动剂(N-803)是治疗复发/难治性头颈部癌的一种新型治疗方式。
我们报告一项I期试验的数据,该试验在既往中位接受过6线治疗后的复发/难治性头颈部肿瘤患者中,采用单倍体相合CIML NK细胞联合N-803,加或不加ipilimumab(IPI)。该试验遵循3 + 3剂量递减设计,主要终点为安全性。通过高分辨率免疫表型和转录组分析,对NK细胞及其在体内的相互作用伙伴进行了表征。
主要安全性终点已确立,10例患者中1例出现剂量限制性毒性。短暂的疾病控制率与供者NK细胞扩增相关,后者与IPI无关。CIML NK细胞联合N-803和IPI与早期NK细胞增殖增加、Treg:Tcon收缩、受者CD8+ T细胞快速恢复以及随后供者NK细胞加速排斥相关。
Cytokine induced memory-like natural killer (CIML NK) cells combined with an IL-15 super-agonist (N-803) are a novel modality to treat relapsed/refractory head and neck cancer.
We report data from a phase I trial of haploidentical CIML NK cells combined with N-803 with or without ipilimumab (IPI) in relapsed/refractory head and neck cancer patients after a median of 6 prior lines of therapy. The trial adhered to a 3 + 3 dose de-escalation design, with primary endpoint being safety. High-resolution immunophenotypic and transcriptional profiling characterized the NK cells and their interacting partners in vivo.
The primary safety endpoint was established, with dose-limiting toxicity in 1/10 patients. A transient disease control rate correlated with donor NK cell expansion, the latter occurring irrespective of IPI. The combination of CIML NK cells with N-803 and IPI was associated with increased early NK cell proliferation, contraction of Treg: Tcon, rapid recovery of recipient CD8 + T cells, and subsequent accelerated rejection of donor NK cells.
CIML NK cells combined with N-803 and ipilimumab to treat head and neck cancer is safe, and associated with a more proliferative NK cell phenotype. However, the combination leads to reduced HLA mismatched NK cell persistence, resulting in an important limitation affecting NK cell combination therapies in clinical trials. These results inform evaluation of CIML NK therapy for advanced malignancies, with considerations for combination with IPI. TRIAL REGISTRATION: NCT04290546.
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