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:PD-1 Inhibition-Trouble for Subsequent TIL Therapy in Patients with Melanoma?
PD-1 Inhibition-Trouble for Subsequent TIL Therapy in Patients with Melanoma?
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为探究抗PD-1治疗经历患者接受过继细胞转移(ACT)疗效较低的原因,我们评估了肿瘤突变负荷(TMB)、预测新抗原频率及TIL(肿瘤浸润淋巴细胞)对新抗原的反应性。即使在TMB相近的患者中,新抗原特异性TIL频率降低仍与ACT应答较低相关,提示PD-1抑制可能对T细胞扩增产生潜在不利影响。另见Levi等发表于第3042页的相关文章。
To explore the lower efficacy of adoptive cell transfer (ACT) therapy in patients with anti-PD-1 experienced melanoma, tumor mutational burden (TMB), predicted neoantigen frequencies, and tumor-infiltrating lymphocyte (TIL) neoantigen reactivity were assessed. Reduced neoantigen-specific TIL frequencies correlated with lower ACT response even in patients with similar TMB, suggesting a potentially harmful effect of PD-1 inhibition on T-cell outgrowth. See related article by Levi et al., p. 3042.
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