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过继性细胞疗法:一种用于胶质母细胞瘤的新型潜在免疫疗法。

Adoptive Cell Therapy: A Novel and Potential Immunotherapy for Glioblastoma.

作者信息

Wang Jingyu, Shen Fang, Yao Ying, Wang Lin-Lin, Zhu Yongjian, Hu Jue

机构信息

Department of Neurosurgery, Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China.

Department of Orthopaedic Surgery's Spine Division, The Affiliated Hospital of Medical School of Ningbo University, Ningbo, China.

出版信息

Front Oncol. 2020 Jan 31;10:59. doi: 10.3389/fonc.2020.00059. eCollection 2020.

Abstract

Glioblastoma multiforme (GBM) is the most common primary brain tumor in adults with very poor prognosis and few advances in its treatment. Recently, fast-growing cancer immunotherapy provides a glimmer of hope for GBM treatment. Adoptive cell therapy (ACT) aims at infusing immune cells with direct anti-tumor activity, including tumor-infiltrating lymphocyte (TIL) transfer and genetically engineered T cells transfer. For example, complete regressions in patients with melanoma and refractory lymphoma have been shown by using naturally tumor-reactive T cells and genetically engineered T cells expressing the chimeric anti-CD19 receptor, respectively. Recently, the administration of ACT showed therapeutic potentials for GBM treatment as well. In this review, we summarize the success of ACT in the treatment of cancer and provide approaches to overcome some challenges of ACT to allow its adoption for GBM treatment.

摘要

多形性胶质母细胞瘤(GBM)是成人中最常见的原发性脑肿瘤,预后极差,治疗进展甚微。最近,快速发展的癌症免疫疗法为GBM治疗带来了一线希望。过继性细胞疗法(ACT)旨在输注具有直接抗肿瘤活性的免疫细胞,包括肿瘤浸润淋巴细胞(TIL)转移和基因工程T细胞转移。例如,分别使用天然肿瘤反应性T细胞和表达嵌合抗CD19受体的基因工程T细胞,已在黑色素瘤和难治性淋巴瘤患者中显示出完全缓解。最近,ACT给药在GBM治疗中也显示出治疗潜力。在本综述中,我们总结了ACT在癌症治疗中的成功经验,并提供了克服ACT一些挑战的方法,以使其能够应用于GBM治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/56af/7005203/3da969b89fa2/fonc-10-00059-g0001.jpg

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