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:Primary Mouse Invariant Natural Killer T (iNKT) Cell Purification and Transduction.
Primary Mouse Invariant Natural Killer T (iNKT) Cell Purification and Transduction.
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恒定自然杀伤T(iNKT)细胞是一种非传统T细胞群体,表达一种保守的半恒定T细胞受体(TCR),可识别由单态分子CD1d呈递的脂质抗原,如α-半乳糖神经酰胺(α-GalCer)。iNKT细胞在肿瘤免疫监视中发挥核心作用,是抗癌治疗的有力工具,尤其因为它们可以通过工程化表达肿瘤特异性嵌合抗原受体(CAR)或TCR而被有效地重定向以对抗血液系统或实体恶性肿瘤。
然而,iNKT细胞数量稀少,需要特定的体外预筛选和大量体外扩增才能用于过继细胞治疗(ACT)。本方案描述了一种稳健的方法,可获得大量小鼠iNKT细胞,并能通过逆转录病毒(RV)转导进行有效工程化改造。本方案的一个主要优势在于既不需要特殊仪器,也不需要大量小鼠。iNKT细胞从iVα14-Jα18转基因小鼠的脾脏中富集;快速纯化方案可获得高度富集的iNKT细胞群体,经抗CD3/CD28磁珠激活,这比使用负载α-GalCer的骨髓来源树突状细胞更具可重复性且更省时,且无扩增污染性T细胞的风险。激活48小时后,通过离心接种法用选定的RV转导iNKT细胞。本方案可在15天内获得数百万个即用型、高度纯化且稳定转导的iNKT细胞,可用于体外实验和临床前研究中的ACT实验。
Invariant natural killer T (iNKT) cells are a non-conventional T-cell population expressing a conserved semi-invariant T-cell receptor (TCR) that reacts to lipid antigens, such as α-galactosyl ceramide (α-GalCer), presented by the monomorphic molecule CD1d. iNKT cells play a central role in tumor immunosurveillance and represent a powerful tool for anti-cancer treatment, notably because they can be efficiently redirected against hematological or solid malignancies by engineering with tumor-specific chimeric antigen receptors (CARs) or TCRs.
However, iNKT cells are rare and require specific ex vivo pre-selection and substantial in vitro expansion to be exploited for adoptive cell therapy (ACT). This protocol describes a robust method to obtain a large number of mouse iNKT cells that can be effectually engineered by retroviral (RV) transduction. A major advantage of this protocol is that it requires neither particular instrumentation nor a high number of mice.
iNKT cells are enriched from the spleens of iVα14-Jα18 transgenic mice; the rapid purification protocol yields a highly enriched iNKT cell population that is activated by anti-CD3/CD28 beads, which is more reproducible and less time consuming than using bone marrow-derived dendritic cells loaded with α-GalCer, without risks of expanding contaminant T cells.
Forty-eight hours after activation, iNKT cells are transduced with the selected RV by spin inoculation. This protocol allows to obtain, in 15 days, millions of ready-to-use, highly pure, and stably transduced iNKT cells that might be exploited for in vitro assays and ACT experiments in preclinical studies.
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