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:Bulk and single-cell transcriptomics identify gene signatures of stem cell-derived NK cell donors with superior cytolytic activity.
Bulk and single-cell transcriptomics identify gene signatures of stem cell-derived NK cell donors with superior cytolytic activity.
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异体自然杀伤(NK)细胞疗法具有显著的安全性和良好的疗效特征,是一种有价值的肿瘤治疗选择。异体供者使现成 NK 细胞产品得以快速用于患者治疗,但供者间固有差异可能影响临床疗效。要确保过继性 NK 细胞治疗成功,识别抗肿瘤活性更强的供者至关重要。
本研究考察了 10 批脐带血干细胞来源 NK 细胞的异质性。首先,我们评估各供者细胞对实体瘤和血液系统肿瘤细胞系的细胞毒性潜力,将其区分为抗肿瘤杀伤表现优异组(4/10)和良好组(6/10)。随后,在 NK 细胞分化的不同阶段进行整体 RNA 测序和单细胞 RNA 测序,发现两组具有不同的转录组特征。优异组的细胞毒性通路富集、髓系特征减少,这与分化早期效应样 NK 细胞群体占比更高有关。据此,我们确定了一种多因素基因表达特征,可用于预测供者的细胞毒性潜力。
本研究有助于识别优质 NK 细胞批次的关键特征,为开发有效的 NK 细胞疗法和实现持久抗肿瘤应答提供支持。
Allogeneic natural killer (NK) cell therapies are a valuable treatment option for cancer, given their remarkable safety and favorable efficacy profile. Although the use of allogeneic donors allows for off-the-shelf and timely patient treatment, intrinsic interindividual differences put clinical efficacy at risk. The identification of donors with superior anti-tumor activity is essential to ensure the success of adoptive NK cell therapies.
Here, we investigated the heterogeneity of 10 umbilical cord blood stem cell-derived NK cell batches. First, we evaluated the donors' cytotoxic potential against tumor cell lines from solid and hematological cancer indications, to distinguish a group of superior, "excellent" killers (4/10), compared with "good" killers (6/10).
Next, bulk and single-cell RNA sequencing, performed at different stages of NK differentiation, revealed distinct transcriptomic features of the two groups. Excellent donors showed an enrichment in cytotoxicity pathways and a depletion of myeloid traits, linked to the presence of a larger population of effector-like NK cells early on during differentiation. Consequently, we defined a multi-factorial gene expression signature able to predict the donors' cytotoxic potential.
Our study contributes to the identification of key traits of superior NK cell batches, supporting the development of efficacious NK therapeutics and the achievement of durable anti-tumor responses.
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