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:Impact of vitamin D plasma levels on in vitro natural killer cell cytotoxicity against non-small cell lung carcinoma in the presence of nivolumab.
Impact of vitamin D plasma levels on in vitro natural killer cell cytotoxicity against non-small cell lung carcinoma in the presence of nivolumab.
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非小细胞肺癌(NSCLC)仍然是癌症相关死亡的主要原因。尽管靶向 PD-1/PD-L1 通路的免疫检查点抑制剂(ICIs)改善了患者预后,但应答差异很大。自然杀伤(NK)细胞对抗肿瘤免疫至关重要,但在肿瘤微环境中常受到抑制。新出现的证据表明,维生素 D 可能影响免疫活性, potentially 增强 NK 细胞细胞毒性并提高 ICI 应答。
本研究在 NSCLC 模型中探讨了 PD-L1 表达、NK 细胞功能与供者维生素 D 水平之间的关系。采用 RIA 测定 63 名志愿者的血清维生素 D 水平,并按维生素 D 状态对供者进行分组获取 NK 细胞。使用 MTT 法在 A549(低 PD-L1)和 HCC827(高 PD-L1)NSCLC 细胞系上检测 NK 细胞毒性,分别在有或无通过 nivolumab 进行 PD-1 阻断的条件下。还分析了性别相关差异。发现供者维生素 D 充足与 NK 细胞对 HCC827 细胞的细胞毒性之间存在显著正相关,但在 A549 细胞中未观察到这种关联。这种效应在血清维生素 D 水平至少为 20 ng/mL 的男性供者中最强,更高水平未带来额外获益。这些发现表明,维持充足的维生素 D 水平可能增强 NSCLC 中 NK 细胞对 PD-1 抑制剂的应答,尤其是在 PD-L1 高表达的肿瘤中。
总体而言,这些结果支持将维生素 D 作为免疫治疗的一种经济可及的免疫调节辅助手段进行探索,并强调了个性化、生物标志物指导治疗策略的重要性。
Non-small cell lung cancer (NSCLC) continues to be a leading cause of cancer-related death. Although immune checkpoint inhibitors (ICIs) targeting the PD-1/PD-L1 pathway have improved patient outcomes, responses vary widely. Natural killer (NK) cells are crucial to antitumor immunity but are often suppressed within the tumor microenvironment. Emerging evidence indicates that vitamin D may influence immune activity, potentially boosting NK cell cytotoxicity and enhancing ICI responses.
This study investigated the relationship between PD-L1 expression, NK cell function, and donor vitamin D levels in NSCLC models. Serum vitamin D levels from 63 volunteers were measured by RIA, and NK cells from donors grouped by vitamin D status. NK cytotoxicity was tested using MTT assays on A549 (low PD-L1) and HCC827 (high PD-L1) NSCLC cell lines, with or without PD-1 blockade via nivolumab.
Sex-related differences were also analyzed. A significant positive correlation was found between donor vitamin D sufficiency and NK cell cytotoxicity against HCC827 cells, but no such link was observed in A549 cells. This effect was the strongest in male donors with serum vitamin D levels of at least 20 ng/mL, with no additional benefit at higher levels.
These findings suggest that maintaining adequate vitamin D levels could enhance NK cell responses to PD-1 inhibitors in NSCLC, especially in tumors with high PD-L1 expression.
Overall, the results support exploring vitamin D as an affordable, immune-modulating adjunct to immunotherapy and highlight the importance of personalized, biomarker-guided treatment strategies.
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