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PLAP-CAR T 细胞对结肠癌细胞具有高特异性细胞毒性。

PLAP -CAR T cells mediate high specific cytotoxicity against colon cancer cells.

机构信息

The Ohio State University.

Promab Biotechnologies, 2600 Hilltop Drive, Building B, Richmond, CA 94806.

出版信息

Front Biosci (Landmark Ed). 2020 Jun 1;25(9):1765-1786. doi: 10.2741/4877.

Abstract

Placental alkaline phosphatase, PLAP encoded by gene in humans is mainly expressed in placenta and testis, and not expressed in any other normal tissues. PLAP is overexpressed in colorectal cancers which makes it an attractive target for CAR (chimeric antigen receptor)-T cell therapy. PLAP mRNA expression was detected in 21.5% (25 out of 116) of colorectal cancer cell lines and this expression was confirmed by FACS at the protein level. In addition, IHC staining on primary colorectal cancer tumors demonstrated PLAP expression in >20% of colorectal cancer tumors. We generated mouse and humanized PLAP ScFv-CAR-T cells and demonstrated high specificity against PLAP-positive colon cancer cells using RTCA (real-time cytotoxicity assay) and IFN-gamma secretion. In addition, humanized-CAR-T cells significantly decreased Lovo xenograft tumor growth . The combination of hPLAP-CAR-T cells with PD-1, PD-L1 or LAG-3 checkpoint inhibitors significantly increased the activity of hPLAP-CAR-T cells. This study demonstrates ability of novel PLAP-CAR-T cells to kill colorectal cancers and that the extent of killing can be increased by combination with checkpoint inhibitors.

摘要

人源基因编码的胎盘碱性磷酸酶(PLAP)主要在胎盘和睪丸中表达,而在其他正常组织中不表达。PLAP 在结直肠癌中过度表达,使其成为嵌合抗原受体(CAR)-T 细胞治疗的一个有吸引力的靶点。在 21.5%(25/116)的结直肠癌细胞系中检测到 PLAP mRNA 表达,这一表达在蛋白质水平上通过 FACS 得到证实。此外,对原发性结直肠癌肿瘤的免疫组化染色显示,超过 20%的结直肠癌肿瘤表达 PLAP。我们生成了小鼠和人源化 PLAP ScFv-CAR-T 细胞,并使用 RTCA(实时细胞毒性测定)和 IFN-γ分泌证明了它们对 PLAP 阳性结肠癌细胞的高特异性。此外,人源化 CAR-T 细胞显著降低了 Lovo 异种移植肿瘤的生长。hPLAP-CAR-T 细胞与 PD-1、PD-L1 或 LAG-3 检查点抑制剂的联合使用显著增加了 hPLAP-CAR-T 细胞的活性。这项研究证明了新型 PLAP-CAR-T 细胞能够杀死结直肠癌,并且通过与检查点抑制剂联合使用可以增加杀伤的程度。

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