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:Phenotypic and functional characterisation of locally produced natural killer cells ex vivo expanded with the K562-41BBL-mbIL21 cell line.
Phenotypic and functional characterisation of locally produced natural killer cells ex vivo expanded with the K562-41BBL-mbIL21 cell line.
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我们表征了用于临床试验的自然杀伤(NK)细胞的扩增、表型和功能活性。共进行了19次扩增程序,为16例患者获取NK细胞产品。NK细胞在局部制备的K-562饲养细胞系(异位表达4-1BBL和mbIL-21)存在下,从单倍体相合供者外周血单个核细胞中进行体外扩增。中位扩增时间为18天(四分位距15-19)。中位活细胞产量为2.26 × 10 9(范围1.6-3.4 × 10 9),NK含量为96.6%(范围95.1-97.9%)。中位NK细胞扩增倍数为171(范围124-275)。NK细胞扩增倍数取决于接种NK细胞数量、C-myc初始表达水平以及成熟和未成熟NK细胞的初始数量。大多数扩增后的NK细胞具有未成熟活化细胞表型(NKG2A +、双阳性CD56 + + CD16 + +、CD57-),表达NKp30、NKp44、NKp46、NKG2D、CD69、HLA-DR和CD96。尽管表达了耗竭标志物,扩增后的NK细胞对白血病细胞系表现出高细胞溶解活性、高脱颗粒活性和细胞因子产生。在针对患者原始细胞的检测中,注意到NK细胞的功能活性下降。
总之,通过使用局部制备的K562-41BBL-mbIL21细胞进行体外扩增获得的NK细胞具有相对未分化的表型,并增强了对癌细胞系的细胞溶解活性。使用饲养细胞扩增NK细胞可产生足够数量的NK细胞产品,以达到高细胞剂量或增加过继免疫治疗中细胞输注的频率。已在ClinicalTrials.gov注册为NCT04327037。
We characterised the expansion, phenotype and functional activity of natural killer (NK) cells obtained for a clinical trial. Nineteen expansion procedures were performed to obtain NK cell products for 16 patients. NK cells were expanded ex vivo from haploidentical donor peripheral blood mononuclear cells in the presence of the locally generated feeder cell line K-562 with ectopic expression of 4-1BBL and mbIL-21. The median duration of expansion was 18 days (interquartile range 15-19). The median number of live cells yielded was 2. 26 × 10 9 (range 1. 6-3. 4 × 10 9 ) with an NK content of 96. 6% (range 95. 1-97. 9%). The median NK cell fold expansion was 171 (range 124-275).
NK cell fold expansion depended on the number of seeded NK cells, the initial level of C-myc expression and the initial number of mature and immature NK cells. The majority of expanded NK cells had the phenotype of immature activated cells (NKG2A + , double bright CD56 + + CD16 + + , CD57-) expressing NKp30, NKp44, NKp46, NKG2D, CD69, HLA-DR and CD96.
Despite the expression of exhaustion markers, expanded NK cells exhibited high cytolytic activity against leukaemia cell lines, high degranulation activity and cytokine production. There was a noted decrease in the functional activity of NK cells in tests against the patient's blasts.
In conclusion, NK cells obtained by ex vivo expansion with locally generated K562-41BBL-mbIL21 cells had a relatively undifferentiated phenotype and enhanced cytolytic activity against cancer cell lines. Expansion of NK cells with feeder cells yielded a sufficient quantity of the NK cell product to reach high cell doses or increase the frequency of cell infusions for adoptive immunotherapy. Registered at clinicaltrials. gov as NCT04327037.
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