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:Melanoma Clonal Heterogeneity Leads to Secondary Resistance after Adoptive Cell Therapy with Tumor-Infiltrating Lymphocytes.
Melanoma Clonal Heterogeneity Leads to Secondary Resistance after Adoptive Cell Therapy with Tumor-Infiltrating Lymphocytes.
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TIL(肿瘤浸润淋巴细胞)过继细胞治疗(ACT)对黑色素瘤患者有效,但持久应答似乎仅限于获得完全缓解的患者。许多患者在TIL-ACT后出现继发性耐药,其机制尚不明确。本研究描述了一例可能由肿瘤内异质性及输注T细胞选择耐药肿瘤细胞克隆所致的TIL-ACT继发性耐药病例。据我们所知,这是首例既存的非优势肿瘤细胞克隆被选择扩增的报告。本病例揭示了TIL-ACT继发性耐药的相关机制,可能改变当前临床实践,因为结果支持治疗前从多个肿瘤部位采集T细胞,并分析肿瘤异质性。
Adoptive cell therapy (ACT) with tumor-infiltrating lymphocytes (TIL) is effective in patients with melanoma, although long-term responses seem restricted in patients who have complete remissions. Many patients develop secondary resistance to TIL-ACT but the involved mechanisms are unclear. In this study, we describe a case of secondary resistance to TIL-ACT possibly due to intratumoral heterogeneity and selection of a resistant tumor cell clone by the transferred T cells.
To the best our knowledge, this is the first case of clonal selection of a pre-existing nondominant tumor cell clone; this report demonstrates the mechanism involved in secondary resistance to TIL-ACT that can potentially change current clinical practice because it advocates for T-cell collection from multiple tumor sites and analysis of tumor heterogeneity before treatment with TIL-ACT.
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