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:Neoantigen-Reactive T Cells: The Driving Force behind Successful Melanoma Immunotherapy.
Neoantigen-Reactive T Cells: The Driving Force behind Successful Melanoma Immunotherapy.
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转移性皮肤黑色素瘤患者在接受检查点阻断免疫治疗或过继细胞治疗后出现了显著的临床反应。新抗原是源自肿瘤特异性突变的突变蛋白。据推测,T细胞对新抗原的识别是T细胞介导的抗肿瘤反应及随后肿瘤消退的关键步骤。除了描述新抗原外,我们还综述了具有开创性及正在进行的临床试验,这些试验有助于塑造目前皮肤黑色素瘤患者的治疗方案。我们还介绍了现有证据,这些证据确立了新抗原反应性T细胞与黑色素瘤免疫治疗临床反应之间的相关性。
Patients with metastatic cutaneous melanoma have experienced significant clinical responses after checkpoint blockade immunotherapy or adoptive cell therapy. Neoantigens are mutated proteins that arise from tumor-specific mutations. It is hypothesized that the neoantigen recognition by T cells is the critical step for T-cell-mediated anti-tumor responses and subsequent tumor regressions.
In addition to describing neoantigens, we review the sentinel and ongoing clinical trials that are helping to shape the current treatments for patients with cutaneous melanoma.
We also present the existing evidence that establishes the correlations between neoantigen-reactive T cells and clinical responses in melanoma immunotherapy.
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