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:Non-invasive cell-tracking methods for adoptive T cell therapies.
Non-invasive cell-tracking methods for adoptive T cell therapies.
分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。
T细胞过继疗法(ACT)在血液系统癌症和黑色素瘤中取得了突破性成果。然而,其成本高、可能发生严重不良事件以及在实体瘤中疗效欠佳,仍是阻碍广泛应用的重要因素。体内细胞追踪可即时、无创地监测患者输注T细胞的分布、肿瘤归巢、持久存续及向其他器官重新分布情况。此外,细胞追踪有助于临床管理,可早期识别无应答患者或严重不良事件。本综述简要介绍细胞追踪的主要原理和潜力,并讨论具有临床应用价值的标记策略及其在ACT中的应用。
Adoptive T cell therapies (ACT) have demonstrated groundbreaking results in blood cancers and melanoma. Nevertheless, their significant cost, the occurrence of severe adverse events, and their poor performance in solid tumors are important hurdles hampering more widespread applicability. In vivo cell-tracking allows instantaneous and non-invasive monitoring of the distribution, tumor homing, persistence, and redistribution to other organs of infused T cells in patients.
Furthermore, cell-tracking could aid in the clinical management of patients, allowing the detection of non-responders or severe adverse events at an early stage. This review provides a concise overview of the main principles and potential of cell-tracking, followed by a discussion of the clinically relevant labeling strategies and their application in ACT.
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