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:4-1BB antibody enhances cytotoxic activity of natural killer cells against prostate cancer cells via NKG2D agonist combined with IL-27.
4-1BB antibody enhances cytotoxic activity of natural killer cells against prostate cancer cells via NKG2D agonist combined with IL-27.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
联合NKG2D激动剂、4-1BB抗体和IL-27,增强自然杀伤(NK)细胞对前列腺癌细胞的细胞毒性。
采用流式细胞分选(FACS)检测健康供者分离NK细胞的脱颗粒和细胞表面受体;采用ELISA测定细胞因子浓度;利用细胞计数试剂盒8分析NK细胞细胞毒性。
联合给予NKG2D激动剂、4-1BB抗体和IL-27,可提高NK细胞活化受体表达及IFN-γ和TNF-α分泌,同时降低抑制性受体CD158a表达和IL-10分泌。该联合处理增强NK细胞对PC3和DU145细胞的细胞毒性,同时提高STAT3活化。
4-1BB抗体和IL-27可增强NKG2D激动剂对NK细胞抗前列腺癌作用的促进效果。
Aims: To enhance the cytotoxicity of natural killer (NK) cells against prostate cancer cells via NKG2D agonist, with 4-1BB antibody and IL-27 combination. Materials & methods: FACS was used to detect degranulation and cell surface receptors in NK cells isolated from healthy donors. Cytokine concentrations were measured using ELISA. NK-cell cytotoxicity was analyzed using Cell Counting Kit-8.
Results: NKG2D agonist, 4-1BB antibody and IL-27 combination treatment improved the activating receptor expression and IFN- and TNF- secretion but decreased the suppressive receptor CD158a expression and IL-10 secretion in NK cells. The combined treatment enhanced NK-cell cytotoxicity against both PC3 and DU145 cells with concurrent enhanced STAT3 activation. Conclusion: 4-1BB antibody and IL-27 improved NKG2D agonist function in NK cells against prostate cancer cells.
MEMBER ACCOUNT
登录成功会直接打开下一页。