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:MICA-specific nanobodies for diagnosis and immunotherapy of MICA(+) tumors.
MICA-specific nanobodies for diagnosis and immunotherapy of MICA(+) tumors.
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MICA 和 MICB 是 I 类 MHC 相关糖蛋白,在细胞受到应激(例如感染或恶性转化)时其表面表达上调。MICA/B 是 NKG2D 的配体,NKG2D 是 NK 细胞、CD8+ T 细胞和 γδ T 细胞上的活化受体。当 MICA/B 与 NKG2D 结合后,这些细胞毒性细胞会清除 MICA/B 阳性的靶细胞。MICA 经常在上皮来源和造血来源的癌细胞表面过表达。在此,我们创建了识别 MICA 的纳米抗体。纳米抗体,即 VHH,是骆驼科重链-only 免疫球蛋白的可变区的重组表达形式。它们保留了抗原识别能力,但以其稳定性和易于生产为特点。本文所述的纳米抗体通过流式细胞术可在体外检测癌细胞表面暴露的 MICA,并且当与美登素衍生物 DM1 融合时,可作为纳米抗体-药物偶联物用于治疗。纳米抗体-DM1 偶联物在体外选择性杀伤 MICA 阳性肿瘤细胞。
MICA and MICB are Class I MHC-related glycoproteins that are upregulated on the surface of cells in response to stress, for instance due to infection or malignant transformation. MICA/B are ligands for NKG2D, an activating receptor on NK cells, CD8 + T cells, and γδ T cells. Upon engagement of MICA/B with NKG2D, these cytotoxic cells eradicate MICA/B-positive targets. MICA is frequently overexpressed on the surface of cancer cells of epithelial and hematopoietic origin.
Here, we created nanobodies that recognize MICA. Nanobodies, or VHHs, are the recombinantly expressed variable regions of camelid heavy chain-only immunoglobulins. They retain the capacity of antigen recognition but are characterized by their stability and ease of production.
The nanobodies described here detect surface-disposed MICA on cancer cells in vitro by flow cytometry and can be used therapeutically as nanobody-drug conjugates when fused to the Maytansine derivative DM1. The nanobody-DM1 conjugate selectively kills MICA positive tumor cells in vitro.
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