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In vivo generated human CAR T cells eradicate tumor cells

机译:在体内产生的人轿厢T细胞根除肿瘤细胞

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摘要

Chimeric antigen receptor (CAR) T cells are in prime focus of current research in cancer immunotherapy. Facilitating CAR T cell generation is among the top goals. We have recently demonstrated direct in vivo generation of human CD19-CAR T cells by targeting CD8+ cells using lentiviral vectors (LVs). The anti-tumor potency of in vivo generated CAR T cells was assessed in human PBMC-transplanted NSG mice carrying i.v. injected CD19+ Nalm-6 tumor cells. A single injection of CD8-targeted LV delivering CD19-CAR was sufficient to completely eliminate the tumor cells from bone marrow and spleen, whereas control animals contained high levels of CD19+ cells. Tumor elimination was due to in vivo generated CAR+ cells. Notably, these were not only composed of T lymphocytes but also included CAR+ natural killer cells (NK and NKT). This is the first demonstration of tumor elimination by in vivo generated human CAR T cells.
机译:嵌合抗原受体(汽车)T细胞是癌症免疫疗法目前研究的主要重点。 促进汽车T细胞的一代是最重要的目标。 我们最近通过使用慢病毒载体(LVS)靶向CD8 +细胞的CD8 +细胞直接在人类CD19-CAR T细胞中展示。 在携带I.V的人PBMC移植的NSG小鼠中评估体内产生的CAR T细胞的抗肿瘤效力。 注射CD19 + NALM-6肿瘤细胞。 单一注射CD8靶向LV递送CD19-X型载体足以完全消除来自骨髓和脾脏的肿瘤细胞,而对照动物含有高水平的CD19 +细胞。 肿瘤消除是由于体内产生的轿厢+细胞。 值得注意的是,这些不仅由T淋巴细胞组成,而且包括Car +天然杀伤细胞(NK和NKT)。 这是第一次通过体内产生的人轿厢T细胞进行肿瘤消除的演示。

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