决定异体 CAR T 细胞排斥与扩增的细胞和分子机制
Cellular and molecular mechanisms determining allogeneic CAR T cell rejection and expansion.
我们评估了11例接受单一批次cemacabtagene ansegedleucel(cema-cel)治疗的大B细胞淋巴瘤患者,cemacabtagene ansegedleucel是一种异体抗CD19 CAR T产品。
英文原题:HER2-specific chimeric antigen receptor-T cells for targeted therapy of metastatic colorectal cancer.
我们的研究提供了科学证据,表明HER2 CAR-T细胞代表了一种新兴的免疫疗法,用于治疗mCRC。
嵌合抗原受体(CAR)-T细胞疗法是一类新型细胞免疫疗法,在恶性肿瘤治疗中取得了巨大成就。尽管结直肠癌(CRC)治疗有所改善,但许多患者因转移和复发而治疗失败。人表皮生长因子受体2(HER2)是CAR-T疗法的确证靶点,近期有报道称其在CRC中过表达,这可能为CRC治疗提供潜在的治疗靶点。在此,通过流式细胞术和包含9年生存随访数据的组织微阵列(TMA)评估,HER2是CAR-T疗法中转移性结直肠癌(mCRC)的一个有前景的靶点。此外,HER2特异性CAR-T细胞在体外对CRC细胞表现出强烈的细胞毒性和细胞因子分泌能力。而且,通过NOD-Prkdc em26cd52 Il2rg em26Cd22 /Nju(NCG)小鼠的荷瘤模型,HER2 CAR-T细胞在三种不同的异种移植模型中显示出有效阻止CRC进展的迹象。值得注意的是,在患者来源的肿瘤异种移植(PDX)模型中,HER2 CAR-T细胞在HER2 + CRC中表现出更强的侵袭性,并在转移性异种移植小鼠模型中对mCRC具有强效的免疫治疗能力。总之,我们的研究提供了科学证据,表明HER2 CAR-T细胞代表了一种用于治疗mCRC的新兴免疫疗法。
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-Prkdc em26cd52 Il2rg em26Cd22 /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.
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