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:KIR2DS2+ NK cells in cancer patients demonstrate high activation in response to tumour-targeting antibodies.
KIR2DS2+ NK cells in cancer patients demonstrate high activation in response to tumour-targeting antibodies.
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动员自然杀伤(NK)细胞对抗癌症的策略包括肿瘤靶向抗体、NK细胞衔接器(NKCEs)以及过继转移体外扩增的健康供者来源NK细胞。遗传学和功能研究已揭示,活化性杀伤细胞免疫球蛋白样受体KIR2DS2的表达与健康供者NK细胞功能增强以及多种不同恶性肿瘤预后改善相关。
然而,目前尚不清楚利用KIR2DS2+ NK细胞进行治疗的最佳策略。因此,在本研究中,我们评估了表达KIR2DS2的NK细胞在临床相关肿瘤靶向抗体激活下以及体外扩增后对抗癌症的反应。
我们发现,与KIR2DS2- NK细胞相比,来自慢性淋巴细胞白血病和肝细胞癌患者的KIR2DS2高表达NK细胞在肿瘤靶向抗体作用下具有增强的活化。
然而,健康供者来源的KIR2DS2高表达NK细胞的优越功能在体外扩增后丧失,而体外扩增是过继转移治疗策略所必需的。这些数据提供证据表明,直接在癌症患者中靶向KIR2DS2可能使其增强的效应功能得以利用,然而这种活性在体外扩增后可能丧失。
Strategies to mobilise natural killer (NK) cells against cancer include tumour-targeting antibodies, NK cell engagers (NKCEs) and the adoptive transfer of ex vivo expanded healthy donor-derived NK cells. Genetic and functional studies have revealed that expression of the activating killer immunoglobulin-like receptor KIR2DS2 is associated with enhanced function in NK cells from healthy donors and improved outcome in several different malignancies.
The optimal strategy to leverage KIR2DS2+ NK cells therapeutically is however currently unclear. In this study, we therefore evaluated the response of KIR2DS2-expressing NK cells to activation against cancer with clinically relevant tumour-targeting antibodies and following ex vivo expansion.
We identified that KIR2DS2 high NK cells from patients with chronic lymphocytic leukaemia and hepatocellular carcinoma had enhanced activation in response to tumour-targeting antibodies compared to KIR2DS2- NK cells.
However, the superior function of healthy donor derived KIR2DS2 high NK cells was lost following ex vivo expansion which is required for adoptive transfer-based therapeutic strategies. These data provide evidence that targeting KIR2DS2 directly in cancer patients may allow for the utilisation of their enhanced effector function, however such activity may be lost following their ex vivo expansion.
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