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:Recent updates on chimeric antigen receptor T cell therapy for hepatocellular carcinoma.
CAR-T 细胞疗法是一种新型肿瘤免疫疗法,通过基因工程技术使T细胞能够特异性识别肿瘤相关抗原,从而发挥抗肿瘤作用,在白血病和淋巴瘤中已取得令人鼓舞的疗效。
CAR-T 细胞治疗是一种新型肿瘤免疫疗法,通过基因工程使 T 细胞特异性识别肿瘤相关抗原并发挥抗肿瘤作用;该疗法已在白血病和淋巴瘤中取得令人鼓舞的疗效。随着相关领域进展,CAR-T 治疗也有望用于实体瘤。肝细胞癌(HCC)是最常见的原发性肝癌,通常确诊时已处于晚期。目前 HCC 治疗选择有限;既往研究虽显示 CAR-T 细胞治疗具有可行性,但尚未达到理想疗效。这部分归因于肿瘤抗原异质性、肿瘤内高压、免疫抑制性微环境、CAR-T 细胞耗竭及严重不良反应,这些因素均会削弱 CAR-T 免疫治疗 HCC 的效果。为克服这些挑战,许多临床前和临床研究正在开展。本综述总结 HCC CAR-T 治疗的现有靶点,讨论当前障碍及可能的解决方案,并介绍提高 HCC 患者 CAR-T 疗效的潜在策略。
Chimeric antigen receptor T cell (CAR-T) therapy is novel tumor immunotherapy that enables T cells to specifically recognize tumor-associated antigens through genetic engineering technology, thus exerting antitumor effects, and it has achieved encouraging outcomes in leukemia and lymphoma. Building on excellent progress, CAR-T therapy is also expected to work well in solid tumors. Hepatocellular carcinoma (HCC), the most common primary liver cancer, is usually diagnosed at an advanced stage. Current management options for HCC remain limited, and although previous studies have indicated the feasibility of CAR-T cells, ideal therapeutic effects have not yet been achieved. This is, in part, due to the heterogeneity of tumor antigens, high intratumor pressure, immunosuppressive microenvironment, CAR-T cell exhaustion, and serious adverse reactions, which compromise the therapeutic efficiency of CAR-T immunotherapy in HCC. To overcoming these challenges, many ongoing preclinical and clinical studies were conducted. This review summarizes current CAR-T therapy targets in the treatment of HCC, discusses current obstacles and possible solutions in the process, and describes potential strategies to improve the efficacy of CAR-T cells for patients with HCC.
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