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针对转移性结直肠癌的靶向治疗的 HER2 特异性嵌合抗原受体-T 细胞。

HER2-specific chimeric antigen receptor-T cells for targeted therapy of metastatic colorectal cancer.

机构信息

School of Public Health, Kunming Medical University, Kunming, 650500, China.

Key Laboratory of Environmental Medicine Engineering, Ministry of Education, School of Public Health, Southeast University, Nanjing, 210009, China.

出版信息

Cell Death Dis. 2021 Nov 27;12(12):1109. doi: 10.1038/s41419-021-04100-0.

DOI:10.1038/s41419-021-04100-0
PMID:34839348
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8627513/
Abstract

Chimeric antigen receptor (CAR) - T cell therapy is a new class of cellular immunotherapies, which has made great achievements in the treatment of malignant tumors. Despite improvements in colorectal cancer (CRC) therapy, treatment of many patients fails because of metastasis and recurrence. The human epidermal growth factor receptor 2 (HER2) is a substantiated target for CAR-T therapy, and has been reported recently to be over-expressed in CRC, which may provide a potential therapeutic target for CRC treatment. Herein, HER2 was a promising target of metastatic colorectal cancer (mCRC) in CAR-T therapy as assessed by flow cytometry and tissue microarray (TMA) with 9-year survival follow-up data. Furthermore, HER2-specific CAR-T cells exhibited strong cytotoxicity and cytokine-secreting ability against CRC cells in vitro. Moreover, through the tumor-bearing model of the NOD-PrkdcIl2rg/Nju (NCG) mice, HER2 CAR-T cells showed signs of effectively preventing CRC progression in three different xenograft models. Notably, HER2 CAR-T cells displayed greater aggressiveness in HER2 CRC in the patient-derived tumor xenograft (PDX) models and had potent immunotherapeutic capacity for mCRC in the metastatic xenograft mouse models. In conclusion, our studies provide scientific evidence that HER2 CAR-T cells represent an emerging immunotherapy for the treatment of mCRC.

摘要

嵌合抗原受体 (CAR) - T 细胞疗法是一种新型细胞免疫疗法,在恶性肿瘤治疗方面取得了巨大成就。尽管结直肠癌 (CRC) 的治疗有所改善,但许多患者的治疗因转移和复发而失败。人表皮生长因子受体 2 (HER2) 是 CAR-T 治疗的一个明确靶点,最近有报道称其在 CRC 中过表达,这可能为 CRC 治疗提供一个潜在的治疗靶点。在此,通过流式细胞术和组织微阵列 (TMA) 评估了 9 年生存随访数据,证实 HER2 是转移性结直肠癌 (mCRC) 的有前途的 CAR-T 治疗靶点。此外,HER2 特异性 CAR-T 细胞在体外对 CRC 细胞表现出强大的细胞毒性和细胞因子分泌能力。此外,通过 NOD-PrkdcIl2rg/Nju (NCG) 小鼠荷瘤模型,HER2 CAR-T 细胞在三种不同的异种移植模型中显示出有效预防 CRC 进展的迹象。值得注意的是,HER2 CAR-T 细胞在患者来源的肿瘤异种移植 (PDX) 模型中对 HER2 CRC 表现出更强的侵袭性,并且对转移性异种移植小鼠模型中的 mCRC 具有强大的免疫治疗能力。总之,我们的研究为 HER2 CAR-T 细胞作为治疗 mCRC 的新兴免疫疗法提供了科学依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ea4/8627513/75c6fbf52847/41419_2021_4100_Fig7_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ea4/8627513/75c6fbf52847/41419_2021_4100_Fig7_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ea4/8627513/c03947c5b677/41419_2021_4100_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ea4/8627513/f57acbef5a19/41419_2021_4100_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ea4/8627513/88ec62188aa9/41419_2021_4100_Fig3_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ea4/8627513/4878671969ea/41419_2021_4100_Fig5_HTML.jpg
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