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:The promising role of engineered T lymphocytes in immunotherapy for high-grade serous ovarian carcinoma: a review of mechanisms, clinical landscape, and future strategies.
高级别浆液性卵巢癌(HGSC)预后不良,复发率约为80%,且存在显著化疗耐药。
高级别浆液性卵巢癌(HGSC)预后差,复发率约80%,且存在显著化疗耐药。常规检查点抑制剂疗效有限(10-15%),因此需要替代性免疫治疗策略。工程化T淋巴细胞,尤其是CAR-T和TCR-T细胞,已成为HGSC的有前景策略。本文献综述探讨了工程化T淋巴细胞在HGSC免疫治疗中的有前景作用。在PubMed、Scopus和Cochrane Library数据库中全面检索了2015年至2025年间发表的经同行评议的研究。检索词包括工程化T淋巴细胞、CAR-T细胞、TCR-T细胞、卵巢癌免疫治疗。CAR-T细胞在HGSC中显示出有前景的临床前抗肿瘤活性,高亲和力T细胞克隆显示出强效疗效。工程化T淋巴细胞在多种疾病背景下展现出有前景的方法。在高级别浆液性卵巢癌中,工程化T淋巴细胞通过协调的颗粒酶/穿孔素和Fas/FasL信号传导调控肿瘤细胞凋亡,从而能够快速细胞毒性清除多个肿瘤靶点。
High-grade serous ovarian carcinoma (HGSC) demonstrates poor prognosis with approximately 80% recurrence rates and significant chemotherapy resistance. Conventional checkpoint inhibitors show limited efficacy (10-15%), necessitating alternative immunotherapeutic approaches. Engineered T lymphocytes, particularly CAR-T and TCR-T cells, have emerged as promising strategies for HGSC. This literature review examines the promising role of engineered T lymphocytes in immunotherapy for HGSC. A comprehensive literature search was conducted across PubMed, Scopus, and Cochrane Library databases for peer-reviewed studies published between 2015 and 2025. Search terms included "engineered T lymphocytes," "CAR-T cells," "TCR-T cells," "ovarian cancer immunotherapy". CAR-T cells demonstrate promising preclinical antitumor activity in HGSC, with high-avidity T-cell clones showing robust efficacy. Engineered T lymphocytes demonstrate promising approaches across disease contexts. In high-grade serous ovarian carcinoma, Engineered T lymphocytes orchestrate tumor cell apoptosis through coordinated granzyme/perforin and Fas/FasL signaling, enabling rapid cytotoxic elimination of multiple tumor targets.
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