免疫检查点阻断通过扩增效应 CD8⁺ T 细胞克隆增强淋巴细胞清除性化疗诱导的抗肿瘤免疫
Immune Checkpoint Blockade Augments Lymphodepleting Chemotherapy-Induced Antitumor Immunity by Expanding Effector CD8+ T-cell Clones.
CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:PRAME Expression: A Target for Cancer Immunotherapy and a Prognostic Factor in Uveal Melanoma.
PRAME Expression: A Target for Cancer Immunotherapy and a Prognostic Factor in Uveal Melanoma.
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我们证实 PRAME 与 UM 的不良预后相关,并与 8q 额外拷贝有强关联。我们表明,在辅助治疗中,PRAME 特异性免疫治疗在包括 UM 在内的恶性肿瘤治疗中具有前景。
葡萄膜黑色素瘤(UM)是一种罕见且死亡率高的疾病,目前正在研究新的治疗选择。黑色素瘤优先表达抗原(PRAME)是一种癌睾丸抗原,在睾丸中表达,但也在包括葡萄膜黑色素瘤在内的癌症中表达。PRAME被认为是多种癌症免疫治疗的靶点,且已证明PRAME特异性T细胞克隆能够杀伤UM细胞。
我们研究了PRAME在血液系统恶性肿瘤和实体恶性肿瘤(包括UM)中表达的文献,以及其作为免疫治疗靶点的作用。我们在来自Leiden University Medical Center(LUMC)的64例患者队列和癌症基因组图谱(TCGA)的80例病例队列中,比较了PRAME高表达与PRAME低表达UM之间的肿瘤特征分布,并在LUMC队列中进行了差异基因表达分析。
PRAME在许多恶性肿瘤中表达,常与不良预后相关,并可作为T细胞受体(TCR)转导T细胞的靶点,这是一种具有高亲和力和安全性的有前景的治疗选择。在UM中,PRAME在26%至45%的病例中表达,并与更差的预后相关。在LUMC和TCGA队列中,PRAME高表达与更大的直径、更高的肿瘤-淋巴结-转移(TNM)分期、更频繁的8q染色体增益以及炎症表型相关。
Uveal melanoma (UM) is a rare disease with a high mortality, and new therapeutic options are being investigated. Preferentially Expressed Antigen in Melanoma (PRAME) is a cancer testis antigen, expressed in the testis, but also in cancers, including uveal melanoma. PRAME is considered a target for immune therapy in several cancers, and PRAME-specific T cell clones have been shown to kill UM cells.
We studied the literature on PRAME expression in hematological and solid malignancies, including UM, and its role as a target for immunotherapy. The distribution of tumor features was compared between PRAME-high and PRAME-low UM in a 64-patient cohort from the Leiden University Medical Center (LUMC) and in the Cancer Genome Atlas (TCGA) cohort of 80 cases and differential gene expression analysis was performed in the LUMC cohort.
PRAME is expressed in many malignancies, it is frequently associated with a negative prognosis, and can be the target of T cell receptor (TCR)-transduced T cells, a promising treatment option with high avidity and safety. In UM, PRAME is expressed in 26% to 45% of cases and is correlated with a worse prognosis. In the LUMC and the TCGA cohorts, high PRAME expression was associated with larger diameter, higher Tumor-Node-Metastasis (TNM) stage, more frequent gain of chromosome 8q, and an inflammatory phenotype.
We confirm that PRAME is associated with poor prognosis in UM and has a strong connection with extra copies of 8q. We show that PRAME-specific immunotherapy in an adjuvant setting is promising in treatment of malignancies, including UM.
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