400016 重庆,重庆医科大学附属第一医院消化内科
Received:24 May 2022,
Revised:2023-03-28,
Published:30 September 2023
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Song WANG, Binglan ZHANG, Bingqiang ZHANG. EpCAM-targeting CAR-T cells against hepatoma cells
Song WANG, Binglan ZHANG, Bingqiang ZHANG. EpCAM-targeting CAR-T cells against hepatoma cells
目的
2
研究靶向上皮细胞黏附分子(epithelial cell adhesion molecule
EpCAM)的嵌合抗原受体T细胞(chimeric antigen receptor-T cells
CAR-T)在体外对数种肝癌细胞的杀伤效能。
方法
2
采用流式细胞术检测4种人肝癌细胞(SK-hep1、hep-G2、HuH7和BEL-7402) EpCAM的表达情况;通过慢病毒载体构建靶向EpCAM的CAR-T细胞;流式细胞术检测CAR分子的表达情况并分析CAR-T的CD3/4/8表型;为分析杀伤效应,将效应细胞和靶细胞共培养后,收集上清液,通过乳酸脱氢酶(lactate dehydrogenase
LDH)释放实验检测LDH释放情况,酶联免疫吸附试验(enzyme-linked immunosorbent assay
ELISA)检测细胞因子IFN-γ和TNF-α的释放情况。
结果
2
EpCAM在hep-G2、HuH7和BEL-7402中高表达,而在SK-hep1中不表达。流式细胞术表明靶向EpCAM-CAR在慢病毒感染后的T细胞中表达率高达43.21%。流式细胞术分析CAR-T细胞CD3/4/8表型,高达95.1%的外周血单个核细胞(peripheral blood mononuclear cells
PBMCs)为CD3阳性,其中CD8
+
T细胞占61.40%、CD4
+
T细胞占32.13%。LDH释放实验提示CAR-T对EpCAM阳性人肝癌细胞hep-G2、HuH7和BEL-7402有更强的直接杀伤能力(
P
<
0.01);ELISA实验提示EpCAM阳性人肝癌细胞hep-G2、HuH7和BEL-7402诱导CAR-T细胞释放更多的IFN-γ和TNF-α(
P
<
0.05
P
<
0.01),而对于EpCAM阴性的SK-hep1肿瘤细胞,CAR-T组与未转染T细胞对照组IFN-γ和TNF-α的释放量无显著差异,此外,这2种细胞因子水平随着E ∶T比值的增加而增加。
结论
2
相对未转染的T细胞,在体外,EpCAM-CAR-T细胞对EpCAM阳性的肝癌细胞具有更强的杀伤能力,能使其释放出更多的LDH、IFN-γ和TNF-α。
Objective
2
To investigate the killing efficacy of chimeric antigen receptor T (CAR-T) cells targeting epithelial cellular adhesion molecule (EpCAM) in several hepatoma cell lines.
Methods
2
Flow cytometry was used to detect the expression of EpCAM in hepatoma cells (SK-hep1
Hep-G2
HuH7 and BEL-7402). After EpCAM -targeting CAR-T cells were constructed using lentiviral vectors with CAR genes
flow cytometry was used to detect the expression of EpCAM-CAR in the obtained cells
and to analyze the CD3/4/8 phenotype of CAR-T cells without transfection of lentiviral vectors. Then the effector cells and target cells were co-cultured
and LDH release assay and ELISA were used to detect the release of LDH and major cytokines in the supernatant.
Results
2
EpCAM was highly expressed in Hep-G2
HuH7 and BEL-7402 cells
but not in SK-hep1 cells. Flow cytometry showed that the expression rate of EpCAM-CAR was 43.21% in CAR-T cells after lentivirus infection. Flow cytometry also indicated that up to 95.1% of peripheral blood mononuclear cells (PBMCs) were CD3 positive
of which 61.40% were CD8
+
T cells and 32.13% were CD4
+
T cells. LDH release assay revealed that the obtained CAR-T cells had stronger direct killing ability on EpCAM-positive hepatoma cell lines Hep-G2
HuH7
and BEL-7402. ELISA showed that EpCAM-positive target cells Hep-G2
HuH7
and BEL-7402 induced CAR-T cells to release more IFN-γ and TNF-α. For SK-hep1 cells with negative EpCAM expression
IFN-γ and TNF-α releases were not significantly different between the CAR-T group and the control group
and the levels of these 2 cytokines werw increased with the increase of E ∶T ratio.
Results
2
Compared with ordinary CAR-T cells
EpCAM-targeting CAR-T cells have a stronger killing effect on EpCAM-positive hepatocellular carcinoma cells.
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