Abramson Cancer Center, University of Pennsylvania, Philadelphia, PA 19104, USA.
Sci Transl Med. 2011 Aug 10;3(95):95ra73. doi: 10.1126/scitranslmed.3002842.
Tumor immunotherapy with T lymphocytes, which can recognize and destroy malignant cells, has been limited by the ability to isolate and expand T cells restricted to tumor-associated antigens. Chimeric antigen receptors (CARs) composed of antibody binding domains connected to domains that activate T cells could overcome tolerance by allowing T cells to respond to cell surface antigens; however, to date, lymphocytes engineered to express CARs have demonstrated minimal in vivo expansion and antitumor effects in clinical trials. We report that CAR T cells that target CD19 and contain a costimulatory domain from CD137 and the T cell receptor ζ chain have potent non-cross-resistant clinical activity after infusion in three of three patients treated with advanced chronic lymphocytic leukemia (CLL). The engineered T cells expanded >1000-fold in vivo, trafficked to bone marrow, and continued to express functional CARs at high levels for at least 6 months. Evidence for on-target toxicity included B cell aplasia as well as decreased numbers of plasma cells and hypogammaglobulinemia. On average, each infused CAR-expressing T cell was calculated to eradicate at least 1000 CLL cells. Furthermore, a CD19-specific immune response was demonstrated in the blood and bone marrow, accompanied by complete remission, in two of three patients. Moreover, a portion of these cells persisted as memory CAR(+) T cells and retained anti-CD19 effector functionality, indicating the potential of this major histocompatibility complex-independent approach for the effective treatment of B cell malignancies.
嵌合抗原受体(CAR)由抗体结合结构域与 T 细胞激活结构域连接组成,可使 T 细胞对细胞表面抗原产生应答,从而克服免疫耐受;但迄今为止,在临床试验中,表达 CAR 的淋巴细胞体内扩增和抗肿瘤效果有限。我们报告,在 3 例晚期慢性淋巴细胞白血病(CLL)患者中,输注靶向 CD19 且包含 CD137 共刺激结构域和 T 细胞受体 ζ 链的 CAR T 细胞,具有较强的非交叉耐药临床活性。在体内,这些经过基因工程改造的 T 细胞扩增超过 1000 倍,归巢至骨髓,并至少在 6 个月内持续高水平表达功能性 CAR。针对靶标的毒性证据包括 B 细胞发育不全以及浆细胞数量减少和低丙种球蛋白血症。平均而言,输注的每个表达 CAR 的 T 细胞可消除至少 1000 个 CLL 细胞。此外,在 2 例患者中,血液和骨髓中均观察到 CD19 特异性免疫应答,同时伴有完全缓解。此外,这些细胞中的一部分作为记忆 CAR(+)T 细胞持续存在,并保留抗 CD19 效应功能,表明这种主要组织相容性复合体非依赖性方法有潜力有效治疗 B 细胞恶性肿瘤。
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