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嵌合抗原受体 T 细胞疗法治疗神经母细胞瘤。

CAR T Cell Therapy for Neuroblastoma.

机构信息

Department of Pediatrics, Stanford University School of Medicine, Stanford, CA, United States.

Stanford Cancer Institute, Stanford University School of Medicine, Stanford, CA, United States.

出版信息

Front Immunol. 2018 Oct 16;9:2380. doi: 10.3389/fimmu.2018.02380. eCollection 2018.

Abstract

Patients with high risk neuroblastoma have a poor prognosis and survivors are often left with debilitating long term sequelae from treatment. Even after integration of anti-GD2 monoclonal antibody therapy into standard, upftont protocols, 5-year overall survival rates are only about 50%. The success of anti-GD2 therapy has proven that immunotherapy can be effective in neuroblastoma. Adoptive transfer of chimeric antigen receptor (CAR) T cells has the potential to build on this success. In early phase clinical trials, CAR T cell therapy for neuroblastoma has proven safe and feasible, but significant barriers to efficacy remain. These include lack of T cell persistence and potency, difficulty in target identification, and an immunosuppressive tumor microenvironment. With recent advances in CAR T cell engineering, many of these issues are being addressed in the laboratory. In this review, we summarize the clinical trials that have been completed or are underway for CAR T cell therapy in neuroblastoma, discuss the conclusions and open questions derived from these trials, and consider potential strategies to improve CAR T cell therapy for patients with neuroblastoma.

摘要

患有高危神经母细胞瘤的患者预后不良,幸存者往往因治疗而留下长期的衰弱后遗症。即使在将抗 GD2 单克隆抗体治疗纳入标准的 upfront 方案后,5 年总生存率仍仅约为 50%。抗 GD2 治疗的成功证明了免疫疗法在神经母细胞瘤中可能有效。嵌合抗原受体 (CAR) T 细胞的过继转移有可能在此基础上取得成功。在早期临床试验中,CAR T 细胞疗法治疗神经母细胞瘤已被证明是安全且可行的,但疗效仍存在显著障碍。这些障碍包括缺乏 T 细胞持久性和效力、难以确定靶点以及免疫抑制性肿瘤微环境。随着 CAR T 细胞工程的最新进展,许多实验室正在解决这些问题。在这篇综述中,我们总结了已完成或正在进行的神经母细胞瘤 CAR T 细胞治疗的临床试验,讨论了这些试验得出的结论和未解决的问题,并考虑了改善神经母细胞瘤患者 CAR T 细胞治疗的潜在策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1535/6232778/14f4174daaba/fimmu-09-02380-g0001.jpg

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